Laryngoscope Investig Oto - 2021 - Goyal - Head and Neck Cancer Survivorship Consensus Statement From The American Head and
Laryngoscope Investig Oto - 2021 - Goyal - Head and Neck Cancer Survivorship Consensus Statement From The American Head and
Laryngoscope Investig Oto - 2021 - Goyal - Head and Neck Cancer Survivorship Consensus Statement From The American Head and
See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
Received: 21 September 2020 Revised: 15 October 2021 Accepted: 10 November 2021
DOI: 10.1002/lio2.702
REVIEW
This manuscript represents a consensus statement from the Survivorship, Supportive Care & Rehabilitation Service of the American Head and Neck Society.
This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any
medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
© 2021 The Authors. Laryngoscope Investigative Otolaryngology published by Wiley Periodicals LLC on behalf of The Triological Society.
Correspondence
Neerav Goyal, Department of Abstract
Otolaryngology—Head and Neck Surgery, The Objectives: To provide a consensus statement describing best practices and evi-
Pennsylvania State University, College of
Medicine, 500 University Drive, H091, dence regarding head and neck cancer survivorship.
Hershey, PA 17033-0850, USA. Methods: Key topics regarding head and neck cancer survivorship were identified
Email: [email protected]
by the multidisciplinary membership of the American Head and Neck Society Survi-
Nishant Agrawal, Section of Otolaryngology—
Head and Neck Surgery, University of Chicago, vorship, Supportive Care & Rehabilitation Service. Guidelines were generated by
Pritzker School of Medicine, 5841 S. Maryland
combining expert opinion and a review of the literature and categorized by level of
Avenue, MC 1035, Chicago, IL 60637, USA.
Email: [email protected] evidence.
Results: Several areas regarding survivorship including dysphonia, dysphagia,
fatigue, chronic pain, intimacy, the ability to return to work, financial toxicity,
lymphedema, psycho-oncology, physical activity, and substance abuse were identi-
fied and discussed. Additionally, the group identified and described the role of key
clinicians in survivorship including surgical, medical and radiation oncologists; den-
tists; primary care physicians; psychotherapists; as well as physical, occupational,
speech, and respiratory therapists.
Conclusion: Head and neck cancer survivorship is complex and requires a multi-
disciplinary approach centered around patients and their caregivers. As survival
related to head and neck cancer treatment improves, addressing post-treatment
concerns appropriately is critically important to our patient's quality of life. There
continues to be a need to define effective and efficient programs that can coordi-
nate this multidisciplinary effort toward survivorship.
KEYWORDS
consensus statement, head and neck cancer, survivorship
1 | I N T RO DU CT I O N While cure rates for advanced-stage HNC remain low, with the
increased incidence of HPV associated tumors, there is a rise in overall
In the modern era, cancer remains a major public health problem HNC survivors in the United States.4
worldwide and remains the second leading cause of death in the In 1985, Dr. Fitzhugh Mullan first described his own personal bat-
United States. In 2020, it is estimated 65,630 new cases of head and tle with cancer and fundamentally changed the concept of survivor-
neck cancer (HNC) will occur, which accounts for 3.6% of new onco- ship. He delineated three key phases of survival: “acute survival,” a
logic cases nationwide.1 period that encompasses diagnosis and treatment; “extended sur-
Well-described risk factors in the development of squamous cell vival,” a period that begins at treatment completion and includes sur-
carcinoma (SCC) include tobacco use and alcohol consumption, which veillance; and “permanent survival,” a period vaguely defined as cure.5
2
traditionally accounted for 90% of HNC cases. In recent years, During this journey, survivors may encounter substantial medical,
human papillomavirus (HPV)-associated oropharyngeal SCC, a biologi- psychosocial, interpersonal, financial, and functional consequences.6
cally unique and clinically distinct disease process, has been shown to As a unique discipline, cancer survivorship has garnered much atten-
encompass as much as 70% of new oropharyngeal carcinoma diagno- tion in recent years, with a renewed focus on continuing care for
ses.3 patients beyond their defined surgery, radiation therapy, and/or che-
After completion of an appropriate diagnostic work-up, which motherapy. Recognizing these changes, the American Head and Neck
includes a complete head and neck physical examination, radiographic Society (AHNS) has convened the AHNS Survivorship, Supportive
imaging, and surgical biopsy, management of HNC is largely driven by Care & Rehabilitation Service, a committee on HNC survivorship. In
the primary anatomic site, TNM (tumor, lymph node, and metastasis) this article, the concept of survivorship is reviewed to identify current
classification, and patient medical comorbidities. Single-treatment practice patterns for HNC patients and gaps in survivor care providing
modalities such as surgery or radiation are typically reserved for the a roadmap for future initiatives in HNC survivorship. We expand upon
30%–40% HNC patients who present with early-stage (I or II) disease. the guidelines set forth by the American Cancer Society (ACS) and the
Multi-modality treatment is reserved for the approximately 60% of American Society of Clinical Oncology (ASCO) with special emphasis
HNC patients presenting with locally or regionally advanced disease.2 placed on the importance of the multidisciplinary model.7,8 The goal
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
72 GOYAL ET AL.
TABLE 1 (Continued)
Abbreviations: BID, body image disturbance; CDT, complete decongestive therapy; CT, computed tomography; EBV DNA, Epstein–Barr virus
deoxyribonucleic acid; HNC, head and neck cancer; HPV, human papillomavirus; OPSCC, oropharyngeal squamous cell carcinoma; PCP, primary care
physician; TSH, thyroid-stimulating hormone.
a
NCCN categories of evidence and consensus.
b
Oxford level of evidence.
of this document is to serve as a guide for head and neck oncologists, transition beyond 5 years after treatment completion to focusing less
primary care clinicians, and allied health care providers treating HNC on cancer surveillance and more on other aspects of survivorship care.
survivors. This clinical advice (summarized in Table 1) has been anno- This section will outline the integration of surveillance and survivor-
tated throughout this article with key recommendations categorized ship concepts during the first 5 years after treatment. During this
by level of evidence, as defined by the University of Oxford Center time, the oncologic treatment team provides close clinical surveillance,
for Evidence-based Medicine (Table 2).9 Recommendations supported augmented by appropriate radiographic imaging and other ancillary
by the National Comprehensive Cancer Network (NCCN) are catego- testing designed to detect disease recurrence while also managing
2
rized differently to incorporate expert consensus (Table 3). treatment-related side effects and other aspects of survivorship. The
use of a formal document to outline the details of the treatment and
outline a survivorship care plan can be helpful and several documents
2 | C A NC E R S U R V E I LL A N C E published by AHNS and ASCO can help accomplish this.6,7 Figure 1
illustrates a timeline of a proposed survivorship care plan based on
A person is considered a cancer survivor from the time of diagnosis the recommendations from this document.
through the balance of his or her life. Although cancer surveillance
and cancer survivorship are often described in an intermingled fash-
ion, they represent distinct concepts.7 Cancer surveillance generally 2.1 | Surgical oncology
refers to surveillance for disease recurrence, progression, or second
primary cancers, often during the first 5 years after treatment comple- During the cancer surveillance period, it is recommended that patients
tion. Cancer survivorship is a broader concept of life-long care that follow-up with their head and neck surgeon at regular, established
also includes intervention for consequences of cancer and treatment intervals after treatment completion. The head and neck surgeon may
including physical and psychosocial effects, coordination of care remain a part of the surveillance team even in those settings where
between primary care providers and specialists, prevention of new the patient received non-surgical treatment. The NCCN has
cancers and late effects, and survivorship care planning.2 For HNC established guidelines for surveillance, entitled “Follow-up Recom-
patients, the relationship between cancer surveillance and cancer sur- mendations” (FOLL-A) under the current Treatment Guideline for
vivorship is an area of active research and will be discussed in Sec- Head and Neck Cancers, which are updated periodically (current
tion 2.5. However, most of the existing medical literature supports a v2.2020—June 2020) and summarized below:
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
74 GOYAL ET AL.
• Patients should be evaluated every 1–3 months in the 1st year 2.2 | Radiation oncology
after treatment; every 2–6 months in the 2nd year after treatment;
every 4–8 months in the 3rd–5th year after treatment; and every Patients are recommended to follow-up with their radiation oncolo-
12 months thereafter (NCCN Category 2A). gists, if they received radiation treatment, throughout the cancer sur-
• Clinic visits should include a complete head and neck examination, veillance period. Timely evaluation of possible persistent or recurrent
indirect mirror and/or flexible fiberoptic laryngoscopy, and nasal locoregional disease after completion of radiation is crucial, as well as
endoscopy for patients with sinonasal malignancies (NCCN Cate- close communication with medical and surgical oncologists. In some
gory 2A). cases, it can be quite challenging to distinguish radiation treatment
• In some cases, initial follow-up after surgical treatment may be effects from disease persistence or recurrence, which may require fur-
more frequent based on symptoms, risk factors, treatment ther evaluation. In addition to performing cancer surveillance, the
sequelae, or physician preference (Oxford Category 5). radiation oncologist will manage acute, subacute, and chronic toxic-
• Consider EBV DNA monitoring for nasopharyngeal carcinoma sur- ities of radiation and evaluate QOL measures as well as health mainte-
veillance (NCCN Category 2B). nance. Many head and neck radiation toxicities are discussed in
• Cancer surveillance visits should also include screening and evalua- Sections 3 and 4, and comprehensive reviews regarding these topics
tion for toxicities, quality of life (QOL) measures, and health main- have recently been published.13,14 These toxicities may be complex
tenance (see Sections 3 and 4). and interrelated; for example, xerostomia may cause secondary dental
• Establishment of survivorship care within 1 year of definitive HNC complications, dysphagia, dietary changes, and depression. A multi-
treatment (NCCN Guidelines: Survivorship). disciplinary team approach to manage these manifestations is critical;
the radiation oncologist should coordinate care with speech-language
Currently, no randomized clinical trials have compared outcomes pathologists, dieticians, dentists, physical therapists, and other special-
in patients following recommended cancer surveillance to those not ists as clinically indicated. At each visit, the radiation oncologist should
adhering to practice guidelines. A recent analysis of 3975 HNC provide patient education and emphasize the importance of routine
patients in Ontario revealed that less than 50% met recommended neck and swallowing exercises.
follow-up guidelines after 2 years of treatment.10 Another study of
esophageal cancer surveillance demonstrated a 9% rate of second pri-
mary with early detection made possible with periodic 2.2.1 | Recommendation
11
nasopharyngolaryngoscopy. Detection of early lesions may also be
aided by advanced optical technology such as high definition fiber Patients who have undergone radiation for HNC should be:
optic imaging, video archiving, and narrow-band imaging.12 Education
and training resources for flexible fiberoptic laryngoscopy can be a. Evaluated for thyroid dysfunction (TSH/T4) every 6–12 months,
found through the American Academy of Otolaryngology and particularly in the setting of neck irradiation (NCCN Category 2A).
OTOSOURCE. While “cure” has traditionally been defined as 5 years b. Referred for regular dental examinations, especially if the patient
of disease-free interval, most patients require at least annual follow- received intraoral or salivary gland irradiation (NCCN Cate-
up beyond 5 years for treatment-related concerns (see Section 2.5). gory 2A).
Similarly, screening for second primaries should also be considered c. Followed in close, alternating intervals, in conjunction with surgical
based on risk factors, including the continuation of tobacco and alco- oncology and medical oncology as outlined in Section 2.1 (NCCN
hol use. Category 2A).
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
GOYAL ET AL. 75
2.3 | Medical oncology induced peripheral neurotoxicity (CIPN). Although poorly understood,
CIPN typically carries a dose-dependent and cumulative relationship,
Medical oncologists are recommended to perform detailed cancer- though patients with pre-existing neuropathy or those receiving dou-
related histories and physical examinations at routine, established blet therapy may develop CIPN at lower doses. CIPN presents as a
intervals throughout the care continuum, including post-treatment “glove and stocking” and its incidence decreases as one is further
surveillance, if the patient received systemic therapy (e.g., chemother- from treatment.15,16 Treatment interventions can include duloxetine,
apy, immunotherapy). Specifically, recognizing and managing the side topical menthol, topical 8% capsaicin, and physical therapy.17–20
effects of commonly utilized chemotherapy agents such as platinum There are no well-defined guidelines and limited medical litera-
agents (i.e., cisplatin, carboplatin, and oxaliplatin), taxanes (paclitaxel ture regarding the timing or frequency of evaluation by medical oncol-
and docetaxel), and vinca alkaloids (vincristine and vinblastine) remain ogy.21 Nonetheless, these assessments should be incorporated into a
challenging, including when patients are afflicted with chemotherapy- shared responsibility surveillance plan with surgical and radiation
oncologists that take into account NCCN guidelines. Establishment of
clinical care pathways that incorporate evidence-based guidelines,
TABLE 3 NCCN categories of evidence and consensus clinical expertise, and program infrastructure/feasibility to integrate
Category 1: Based upon high-level evidence, there is uniform NCCN multidisciplinary care, cancer surveillance, and care transitions should
consensus that the intervention is appropriate. also be considered.21 A shared surveillance plan may also serve to
Category 2A: Based upon lower-level evidence, there is uniform reduce patient burden on individual specialties, thus permitting
NCCN consensus that the intervention is appropriate. improved patient access. In addition to cancer surveillance and toxic-
Category 2B: Based upon lower-level evidence, there is NCCN ity monitoring, the role of medical oncology evaluations could also be
consensus that the intervention is appropriate.
viewed as a potential facilitator of improved health promotion and
Category 3: Based upon any level of evidence, there is major NCCN care coordination with primary care physicians (PCPs) and survivor-
disagreement that the intervention is appropriate.
ship clinics to potentially minimize health care fragmentation.22
FIGURE 1 A proposed timeline depicting the timing of the different assessments suggested by these guidelines
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
76 GOYAL ET AL.
prefer specialist-led care.31,32 This represents a recognition on the assessment of baseline function may help identify patients at risk of
part of patients that oncologists familiar with the survivor, cancer chronic dysfunction and those who may require additional assistance
type, and treatment regimen are better equipped to understand late for nutritional needs (i.e., gastrostomy tube) or for phonatory rehabili-
sequelae of disease and associated treatment. Ideally, survivorship tation (i.e., alaryngeal speech). In patients receiving radiotherapy or
care would be provided by a team consisting of nurses, advanced chemoradiation therapy, SLP providers may teach and encourage pro-
practice providers, oral health care providers, medical oncologists, phylactic swallowing exercises that may improve post-treatment func-
radiation oncologists, and/or surgical oncologists working in close tional outcomes.43,44 In such patients, swallowing exercises that help
33
coordination with the patient's primary care provider. maintain oral intake through the treatment phase are associated with
better long-term swallowing outcomes and reduced gastrostomy tube
dependence.45
2.5.1 | Recommendation Patients with HNC also experience difficulties with speech and
voice production that may include a spectrum of presentations:
Patients who are beyond 5 years of HNC treatment and are desig- impaired intelligibility to poor quality of voice or loss of natural
nated as survivors may be: speech. Speech therapy may certainly improve speech quality and
intelligibility.46 SLP providers may also help identify optimal strategies
a. Followed by a multidisciplinary team consisting of nurses, for speech rehabilitation and restoration in alaryngeal patients via an
advanced practice providers, oral health care providers, medical electrolarynx, tracheoesophageal puncture, or esophageal speech.
oncologists, and/or radiation oncologists, in conjunction with the As a result, early referral to SLP providers should be considered
annual follow-up with surgical oncologists, working in close coordi- for patients with HNC as part of their evaluation and treatment plan-
nation with the patient's primary care provider on at least an ning. SLP professionals may play a role in ongoing survivorship care
annual basis (NCCN Category 2A). for patients through surveillance of functional outcomes related to
speech and swallowing. Symptom driven assessment tools including
modified barium swallow study, fiberoptic endoscopic evaluation of
3 | Q U A LI T Y O F L I F E swallowing, and videostroboscopy provide insights into developing
targeted interventions including the teaching of compensatory
3.1 | Dysphonia and dysphagia maneuvers and swallowing exercises when needed.41 Given the
potential for development of late toxicities in patients receiving radia-
Patients affected by HNC commonly experience symptoms related to tion therapy, long-term evaluation of cranial nerve function, speech,
compromised speech, voice, and swallowing function and thus experi- and swallowing are indicated.
ence diminished QOL. Speech and swallowing impairments may arise
from the intrinsic neoplastic process or resultant sequelae of therapy
including surgery, radiation, and/or chemoradiation therapy.34 Factors 3.1.1 | Recommendation
such as anatomic alterations, dentition loss, xerostomia, trismus,
mucositis, post-treatment lymphedema, fibrosis, and neuropathy may Patients who have been diagnosed with HNC, particularly of the
detrimentally influence a person's ability for mastication, deglutition, aerodigestive tract, should be:
and nutritional maintenance.35,36
Symptoms of swallowing disturbance are common among a. Referred to SLP providers for evaluation and management of
patients with HNC. In one SEER based study, the prevalence of dys- speech, voice, and swallowing symptoms (NCCN Category 2A).
phagia, stricture, and aspiration pneumonia was 45.3%, 10.2%, and b. Referred to SLP, if possible, prior to the initiation of therapy to
8.7%, respectively. The prevalence of these signs and symptoms was optimize post-treatment communication and swallowing outcomes
modified by site (lower in oral cavity), stage (higher with more (NCCN Category 2A).
advanced cancers), and by treatment modality (higher in patients
receiving non-surgical or multiple treatment modalities).37 Other stud-
ies suggest that nearly one in two patients experience poor QOL due 3.2 | Fatigue
to dysphagia and that up to 84% of patients may experience aspira-
tion.38,39 The addition of chemotherapy as a radiosensitizer may fur- Cancer-related fatigue is a distressing, persistent, and subjective sense
40
ther exacerbate these symptoms. of physical, emotional, and/or cognitive tiredness or exhaustion
Collaborative multidisciplinary efforts centered on the patient's related to cancer or oncologic treatment that is not proportional to
ability to preserve and recoup functional speech and swallowing may recent activity and interferes with normal function.47 Typically, can-
produce improvements in QOL.41 SLP providers may help identify cer-related fatigue is not relieved by rest or sleep. Most patients diag-
baseline speech and swallowing disturbances and provide education nosed with HNC experience cancer-related fatigue, particularly when
and counseling that may help patients understand the implications of treatment includes radiation or chemoradiation.48,49 Symptoms
42
their disease and its impact on speech and swallowing. This related to fatigue peak early (i.e., within 8 weeks) after initiation of
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
78 GOYAL ET AL.
radiation, with persistent or worsening of symptoms over the first head and neck-specific intimacy questionnaire is created. Referral for
2 years following therapy and contribute to a significant loss of psychosexual therapy may be beneficial in some circumstances.57
48
QOL. Individuals treated with irradiation to the skull base are at risk of
Fatigue may arise from a variety of underlying medical conditions hypothalamic–pituitary axis disorders.58 Specifically, up to 20% of
that may coexist with the diagnosis of HNC. This includes baseline patients treated with radiotherapy for nasopharyngeal carcinoma may
frailty, anemia, anxiety, depression, poor cardiopulmonary reserve, experience hypogonadism.59 As this can have profound effects on sex-
malnutrition, psychological distress, sleep disturbances, thyroid dys- ual function, it is encouraged that these patients undergo regular assess-
function, pain related to cancer and/or its therapy, pro-inflammatory ment of hypothalamic–pituitary function (e.g., screening for symptoms,
or catabolic state, and substance abuse.50 Patients with a history of laboratory testing) with referral to endocrinology as indicated.
HNC can be counseled and screened for fatigue upon initial evalua-
tion and then periodically through their survivorship.47 Patients identi-
fied with symptoms of fatigue should be assessed for underlying 3.3.1 | Recommendation
medical conditions through a comprehensive review of history, physi-
cal examination, appropriate hematology and biochemical testing (i.e., Patients who have undergone treatment for HNC should be:
complete blood count, comprehensive metabolic panel, thyroid func-
tion testing, and nutritional markers), use of screening tools for psy- a. Screened for sexual and intimacy dysfunction, possibly using ques-
chologic distress and depression, and referral to specialists when tionnaires (Oxford Category 2A).
appropriate. b. Offered referrals for therapy for sexual function and intimacy
In addition to counseling and treatment of comorbid medical con- issues (Oxford Category 2A).
ditions contributing to fatigue, patients should be encouraged to par- c. Assessed for pituitary dysfunction if they have received skull base
ticipate in a regular exercise regimen.50,51 Physical therapists irradiation (Oxford Category 2A).
specializing in oncology care can provide treatment to address cancer-
related fatigue. Additionally, clinicians and patients may consider the
use of cognitive-behavioral therapy, yoga, massage therapy, and 3.4 | Chronic pain
others to mitigate cancer-related fatigue.47,52
Chronic pain may be present in up to 45% of patients treated for
HNC.60,61 This can have profound effects on function and QOL
3.2.1 | Recommendation among HNC survivors. There is no clear universally accepted or stan-
dardized tool for assessing chronic pain in patients with HNC. Likert
For patients who have undergone treatment for HNC: scales or validated QOL instruments may be utilized as adjuncts to
better assess the degree of disability experienced by the patient as a
a. Consider evaluating for underlying etiologies of fatigue by the mul- result of pain.62 Over 20% of patients with chronic pain meet criteria
tidisciplinary care team (Oxford Category 5). for a major depressive episode.60 Patients should be evaluated for
depressive symptoms and referred accordingly in this context.
While pain is most often associated with treatment sequelae, it
3.3 | Sexual dysfunction and intimacy can also be a harbinger of recurrent disease. Up to 70% of patients
with recurrent carcinoma will present with pain as the first symp-
HNC and its associated treatment can have significant physical, psy- tom.63 A comprehensive examination of the upper aerodigestive tract
chosocial, and emotional consequences which may adversely affect is imperative in the context of chronic post-treatment pain—particu-
sexual function and intimacy. Patients and partners report a signifi- larly in the setting of lancinating focal pain that radiates to the unilat-
cantly reduced frequency of vaginal and oral sex practices after treat- eral auricle or mandible.
ment for head and neck carcinoma regardless of HPV status.53 Up to Though definitions vary in the literature, a generally accepted def-
44% of patients treated for upper aerodigestive malignancies report inition of chronic pain is pain that extends beyond 3 months beyond
at least some difficulty with sexual function and/or intimacy following the acute phase of treatment—provided that the acute effects of ther-
treatment.54 Furthermore, patients perceive that their questions and apy have resolved.64 Thirteen to fifty percent of patients undergoing
concerns regarding intimacy and sexuality are not being addressed by HNC-directed therapy with curative intent will utilize opioids chroni-
their oncology team. This is most significant among those treated for cally. Chronic use and abuse following treatment are associated with
tumors that do not have a direct effect on fertility and urogenital pre-treatment opioid use, alcohol disorders, and nicotine dependence,
function.55 At the same time, no validated tool exists to address sex- as well as the employment of induction chemotherapy or tri-modal
ual function and intimacy among individuals specifically treated for therapy. Furthermore, depression and anxiety are associated with
56
HNC. At this time, several oncologic and HNC-related quality of life chronic opioid use after cancer treatment.60,65–67 Chronic opioid use
instruments do include items that pertain to sex and intimacy (e.g., has also been associated with decreased disease-free survival among
FACT-HN)56; these may be utilized as screening tools until a validated patients with oral cavity carcinoma.68
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
GOYAL ET AL. 79
Given the opioid crisis that currently exists, patients (particularly commonly encountered post-treatment. Baseline assessment of
those in high-risk groups) should be screened for chronic opioid use shoulder, temporomandibular joint, and neck mobility should be com-
and abuse at 3 months after completion of treatment. Opioid alterna- pleted before therapy and at routine post-treatment visits as a com-
tives with demonstrated success in managing chronic pain include ponent of a comprehensive physical examination by HNC providers.
nonsteroidal anti-inflammatory drugs and acetaminophen. The prevalence of shoulder dysfunction after neck dissection has
Neuromodulators, such as gabapentin, have also demonstrated effi- been variably reported and is associated with the extent of surgery.
cacy in the management of acute treatment-related pain during HNC One meta-analysis demonstrated impaired abduction is observed in
therapy.69,70 and in managing chronic cancer-related pain.71 greater than 90% of patients undergoing radical neck dissection and
For those patients whose chronic opioid use or pain refractory to 23% of patients undergoing modified radical neck dissection.77 Objec-
non-opioid therapy remains a concern, referral to a palliative care or tive assessment of shoulder strength and range of motion may be per-
multidisciplinary pain management team is recommended. These spe- formed using the standard Medical Research Council “0–5” scale and
cialized teams typically take a more holistic approach toward chronic a handheld goniometer, but may not be practical to execute in a surgi-
pain and can provide integration of pharmacotherapy, physiotherapy, cal clinic.78,79 Several patient-directed questionnaires regarding shoul-
psychotherapy, and non-traditional resources. These wide-ranging der function after neck dissection have been developed to quantify
treatment modalities may be beneficial in reducing opioid depen- disability and assess rehabilitation needs.80 One review noted that the
72,73
dence, cost, and pain-related morbidity in certain contexts. Neck Dissection Impairment Index is the only patient-reported out-
come scale to specifically address shoulder function in patients who
have undergone neck dissection.80
3.4.1 | Recommendation When subjective or objective shoulder dysfunction is identified,
the efficacy of physiotherapy is somewhat equivocal based upon the
Patients who have undergone treatment for HNC should be: existing medical literature. McGarvey and colleagues noted in a 2011
review that while well-tolerated by patients, there is little evidence to
a. Screened by the survivorship team for chronic pain at routine suggest that physical therapy is effective in ameliorating shoulder dys-
intervals (NCCN Category 2A). function after neck dissection.81 This same group published a follow-
b. Assessed for the quality and severity of their pain using pain up study in which patients were prospectively randomized to either a
assessment tools by the team (NCCN Category 2A). 12-week shoulder strength program or a control group after neck dis-
c. Evaluated for depressive symptoms in the presence of chronic pain section. They found that the group enrolled in physical therapy had
by the team (NCCN Category 2A). significant improvements in active abduction of the shoulder at
d. Undergo comprehensive evaluation to rule out recurrent disease 3 months postoperatively.82
as a cause of their pain by the team (Category 3B). With advancements in radiation therapy, transverse myelitis fol-
e. Screened for opioid abuse by the team (NCCN Category 2A). lowing HNC treatment is very uncommon (<1% at 54 Gy with con-
f. Offered non-opioid analgesics including nonsteroidal anti- ventional fractionation).83 However, mild spinal cord toxicity can
inflammatory agents, acetaminophen (Oxford Category 2C), occur in the form of L'Hermitte's sign, which is characterized as elec-
neuromodulators (NCCN Category 2A), and acupuncture (Oxford tric-shock sensations down the spinal cord and into the extremities
Category 1A) through palliative and/or pain management consulta- upon neck flexion.84 With historical conformal, field-based radiation
tions by the team. therapy for HNC, rates between 3% and 13% are reported.85 Interest-
g. Referred to palliative and/or pain management specialists for ingly, recent work focusing on intensity-modulated radiation therapy
refractory or opioid-dependent pain (Oxford Category 5) by for thoracic and head and neck malignancy describes an increased
their team. incidence of L'Hermitte's sign between 15% and 29%. Typically,
L'Hermitte's sign develops in the first few months following radiation
therapy and seldom lasts more than 6 months.86 Treatment for
3.5 | Physical therapy patients suffering from this condition remains conservative in nature,
including a soft neck collar, corticosteroids, and hyperbaric oxygen.87
Functional musculoskeletal limitations after HNC-directed therapy are Trismus is variably defined but has been most compellingly vali-
relatively common, though often under-reported and under-treated. dated at a 35 mm inter-incisor distance.88 Among patients with oral
The subsequent disability can result in significant reductions in QOL cavity or oropharyngeal primary tumors, studies estimate that 25%–
and livelihood of HNC survivors. Indeed, a minority of HNC multi- 40% of patients will develop trismus post-therapy with risk factors
disciplinary teams refer patients for physical therapy on a routine including the initial tumor stage, need for reconstruction, receipt of
basis.74 The most common musculoskeletal issues include shoulder chemotherapy, and the receipt of radiation.89,90 Three recent system-
dysfunction, seen in up to 70% of patients undergoing neck dissec- atic reviews note that trismus is improved by exercise therapy and that
tion, and trismus, which may be observed in up to one-half of patients early initiation and compliance resulted in more favorable outcomes. In
undergoing radiotherapy to the pterygoid musculature/temporoman- one review the TheraBite device increased mouth opening significantly
dibular joint region.75,76 Diminished neck range of motion is also with an effect size of 2.6 compared to tongue blades (1.5), forced
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
80 GOYAL ET AL.
opening (1.1.), or microcurrent therapy (0.3). However, a return to nor- Treatment of lymphedema involves improving lymphatic drainage
mal (i.e., >35 mm) levels was not feasible in most cases.91–93 through manual massage and compressive bandages. Manual lym-
phatic drainage (MLD) employs gentle circular massage to improve
lymphatic flow. Complete decongestive therapy (CDT) represents the
3.5.1 | Recommendation “gold standard” for management; it combines MLD, exercise, skincare,
and compressive bandages and is performed by certified lymphedema
Patients who have undergone treatment for HNC may need to be: therapists. This therapy often involves intense, near-daily outpatient
therapy for the first 2–4 weeks followed by a transition to home ther-
a. Screened for physical rehabilitation needs early in the post-treat- apy; however, a motivated patient or caregiver may be able to provide
ment phase and at regular intervals by their survivorship team appropriate and effective home care if frequent clinic visits are not
(Oxford Category 5). feasible.101 Exercises include range of motion exercises of the face,
b. Assessed for trismus, depending on the site of their cancer, before neck, shoulders, and arms as well as swallowing exercises. The com-
and at regular intervals following therapy by their survivorship pressive bandages are often applied after MLD, though some institu-
team (NCCN Category 2A). tions support applying the bandages before and after MLD.94 These
c. Referred to exercise and physiotherapy professionals for struc- therapies are effective in managing lymphedema in HNC patients.102
tured rehabilitation after HNC treatment by their survivorship
team (Oxford Category 5).
d. Undergoing shoulder physiotherapy after completion of neck dis- 3.6.1 | Recommendation
section as early as feasible by their survivorship team (Oxford Cat-
egory 1B). Patients who have undergone treatment for HNC should be:
3.7.2 | Distress, depression, and anxiety a. Screened for BID concerns by their survivorship team (NCCN Cat-
egory 2A).
Distress, depression, and anxiety are prevalent in HNC survivors, who b. Referred to psychology or psychiatry for the management of BID
are at higher risk for developing psychological sequelae than survivors as indicated by their team (NCCN Category 2A).
with other types of cancer.116 As a result, HNC survivors should be c. Assessed for distress, depression, and/or anxiety at regular inter-
assessed periodically for distress, depression, and anxiety using vali- vals with a validated questionnaire by their team (Oxford Cate-
dated screening tools (e.g., NCCN Distress Thermometer, Hospital gory 1A).
Anxiety and Depression Scale, Beck Depression or Anxiety Invento- d. Referred to psychology or psychiatry if distress, depression, and/or
ries, Generalized Anxiety Disorder-7, and Patient Health Question- anxiety are present (Oxford Category 1B).
naire-9).7,117–119 For survivors with clinical findings of distress,
depression, or anxiety, recommended treatments include psychother-
apy, pharmacotherapy, and referral to psycho-oncology. Unfortu- 3.8 | Hearing loss
nately, mental health support is frequently underutilized.7,120 There is
evidence that preventative interventions, before initiation of HNC HNC treatment can have a profound impact on auditory function. For
treatment, may decrease the risk of depression in HNC survivors. A cancers involving the ear, nasopharynx, skull base, and paranasal
landmark trial found that prophylactic escitalopram given to HNC sinuses, both surgery and radiation can have a significant effect on
patients at treatment initiation reduced the risk of depression by more the auditory pathway. Surgical resection of the external auditory canal
than 50%, with beneficial effects seen primarily in those treated with (EAC), tympanic membrane, and/or middle ear space will result in con-
121
definitive radiation-based approaches. Other multidisciplinary HNC ductive hearing loss (CHL). Similarly, surgery of the paranasal sinuses,
programs have integrated health psychologists in the multidisciplinary nasopharynx, and/or skull base can lead to trauma, edema, or dysfunc-
treatment team to aid in pre-treatment evaluation and identification tion of the Eustachian tube leading to CHL from serous otitis media.
of psychosocial risk factors, with close follow-up with intervention as Radiation therapy to the head and neck may also lead to both
indicated. This integration has been well received by patients, care- CHL and sensorineural hearing loss (SNHL). CHL may result via radia-
givers, and medical professionals.122 tion changes to the Eustachian tube apparatus, additionally, external
Although the body of literature remains small for HNC, there is evi- toxicity to the auricle or EAC may lead to otitis externa, EAC stenosis,
dence to suggest support group participation in patients with breast, or ossicular necrosis.129,130 Radiation to the inner ear can also lead to
lung, and colon cancer has been found to decrease anxiety and depres- SNHL anywhere along the auditory pathway from the brainstem to
sion.123 Furthermore, with the advent of internet technology, virtual the cochlea. Studies have identified that the incidence of ototoxicity
support groups have been associated with reductions in physiological is associated with radiation dose and technique, patient age, and the
and psychological stress.124 Online gatherings can promote social sup- combination of radiation with chemotherapy. Studies suggest a radia-
port by increasing functional status, personal empowerment, and self- tion dose greater than 40–45 Gy to the cochlea may be associated
esteem as well as decrease feelings of depression, emotional distress, with a higher incidence of irreversible ototoxicity, though some have
helplessness, and social isolation.125 In a study of 199 patients with described SNHL with radiation doses as low as 20–25 Gy.130–134
HNC, better health-related QOL was associated with being a member Reports of ototoxicity also range from 0% to 43% including a variety
of an online support group for a longer period (B = 0.07, p < .05). With of radiation techniques.131,132,135
these notable benefits, health care professionals should certainly Chemotherapy, particularly platinum-based agents (primarily cis-
encourage and refer patients to seek out regional and support groups platin but also carboplatin and oxaliplatin), can have strong effects on
and information related to their clinical condition. the inner ear and may result in high-frequency SNHL and tinnitus.129
Given the tremendous psychosocial burden of HNC for survivors, These drugs have a cumulative dose-dependent effect; a total dose of
suicide is a critically important issue.126 Up to 16% of HNC survivors more than 100 mg/m2 of cisplatin places patients at risk for develop-
report suicidal ideation within the first year, with the highest risk ing high-frequency SNHL.7 Ototoxic effects related to chemotherapy
being in those with substance abuse and prior psychiatric disor- can be characterized by cochlear dysfunction (hearing loss, tinnitus, or
127
ders. The adjusted suicide risk in HNC survivors ranges from 38 to hyperacusis), vestibular dysfunction (vertigo, dizziness, or imbalance),
60/100,000 person-years; HNC survivors are 2-fold more likely to die or a combination of phenomena.136 Tinnitus, defined as a subjective
from suicide than patients with other types of cancer and 3-fold more perception of sound without an external source can lead to a signifi-
likely than the general US population.27,128 Even more concerning, the cant negative impact on psychological status and QOL; it has been
27
risk of suicide in HNC survivors is increasing over time. There is thus estimated that 40% of patients receiving chemotherapy develop tinni-
an urgent need to develop novel strategies to prevent suicide in HNC tus.137 Vestibular symptoms can trigger a deterioration of QOL includ-
127
survivors and integrate them into routine clinical care. ing interference with driving, riding a bicycle, and other activities as
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
82 GOYAL ET AL.
well as psychological symptoms.138 Hearing loss related to caregiver unmet needs, which often differ from and are put aside for
cochleotoxicity may present immediately or in a delayed fashion and those of the survivor.154,155 These unmet needs include balancing com-
can be progressive, affecting as many as 18% of patients who under- peting roles/responsibilities, making time for self-care, finding effective
went cisplatin therapy.139 The presence of hearing loss in the middle strategies for encouraging patient self-care, changes in intimacy and
of treatment may lead to consideration for an alternative chemother- social/leisure activities, fears/anxiety regarding cancer recurrence, and
apy regimen. the lack of coping strategies for others not acknowledging “the impact
Chemoprotective agents have been studied, though none are that having a partner experience cancer has had on my own life.” These
standard of care.129 Treating and managing ototoxicity are dependent findings suggest the need for information, counseling, and reassurance
on the cause and location. CHL secondary to edema will often resolve that partners and caregivers may require through education, interven-
over time, while losses secondary to scarring/fibrosis or Eustachian tions, and sharing of assessment and management plan by the clinicians.
tube dysfunction may require surgical approaches to relieve the focal It is important to encourage caregivers to pause and take the time to
obstruction. Serous otitis media may also resolve over time but those take care of themselves, as this will allow them to continue taking care
patients with persistent CHL for 3–6 months may benefit from either of HNC survivors. Caregivers should be encouraged to seek help from
simple myringotomy or tympanostomy tube placement.129 Unfortu- others, recognize the limits of their abilities and endurance, and take
nately, there is no established treatment for SNHL with mixed results pride in the care they provide for HNC survivors. For physical health
associated with high-dose steroid administration or hyperbaric oxygen maintenance, they should similarly see their PCP regularly, adopt a
therapy. As outlined by the American Academy of Audiology, patients healthy active lifestyle, and undergo routine age-appropriate and gender-
undergoing platinum-based chemotherapy should undergo pure tone appropriate cancer screening. For mental health concerns, care-
audiometry a few months following completion of chemotherapy givers should be counseled on a wide variety of emotions, such as
followed by monitoring for at least 2 years in the setting of concomi- guilt, anger, depression, and anxiety, particularly around the fear of
tant radiation therapy as hearing loss may progress over time (https:// cancer recurrence. Caregivers should also be encouraged to speak
www.audiology.org/publications-resources/document-library/ openly to their loved ones or talk with a counselor, the oncology
ototoxicity-monitoring). In addition, post-treatment SNHL rehabilita- team, PCP, close friends, or support groups. There remains an
tion relies on the use of hearing amplification (hearing aids).131 For important clinical need for additional research to develop effective
patients with profound bilateral SNHL, cochlear implantation is effec- supportive interventions targeting the unique concerns of HNC
tive with no difference in outcomes as compared to those who did caregiver–survivor dyads.156–159
129,131
not previously receive chemotherapy or radiation.
3.9.1 | Recommendation
3.8.1 | Recommendation
Care of patients who have undergone treatment for HNC should be:
Patients who have undergone platinum-based chemotherapy and/or
radiation therapy for HNC should be: a. Inclusive of partners and caregivers in all aspects of HNC care pro-
vided by the oncology team (Oxford Category 5).
a. Evaluated yearly for hearing loss via pure tone audiometry for at
least 2 years (NCCN Category 2A).
3.10 | Social support groups
Patients who have undergone treatment for HNC should be: As a result of the convergence between improved oncologic out-
comes, increased cost of cancer care, and continued shifting of cost
a. Educated by their survivorship team on social support groups and burden to the patient, there has been a growing awareness of the
their impact on understanding the wide-ranging sequelae of onco- devastating financial toxicity that can burden HNC survivors and their
logic treatment (Oxford Category 5). caregivers.165,166 Financial toxicity is a multidimensional construct: (1)
material hardship that results from increased out-of-pocket costs and
lower-income, (2) psychological distress resulting from material hard-
3.11 | Return to work ship, and (3) compensatory coping strategies that families develop in
response to the financial cost of cancer and its treatment.167,168
Returning to work after cancer treatment can be a daunting task for Patients with HNC are disproportionately burdened by the destruc-
patients. For HNC patients, simple tasks such as eating in public, tive consequences of financial toxicity relative to other types of cancer165
fatigue, radiation dermatitis, and oral ulcers can make functioning in a HNC-related financial toxicity is especially common, with cumulative inci-
public work environment difficult and at times, embarrassing. Due to dence estimates ranging from 40% to 69%.169,170 Patients with HNC
the impact on the patient's speech and voice, communication may be who are particularly high-risk include those with Medicaid, decreased
difficult with coworkers and performing daily work-related duties. It is wealth, higher perceived social isolation, and higher total out-of-pocket
imperative for employers to support the employees' successful return treatment costs.165,170 Financial toxicity is thus yet another aspect of the
to work and provide them engagement opportunities or accommoda- cancer care continuum in which significant and disturbing disparities in
tions to change the nature of their job. Cancelliere and colleagues outcomes exist.166 Financial toxicity can be assessed using quantitative
demonstrated common factors associated with positive return to measures (e.g., financial burden, ratio of out-of-pocket health-related
work outcomes include higher education and socioeconomic status, spending to household income) or patient-reported measures such as the
higher self-efficacy and optimistic expectations for recovery and Comprehensive Score for financial Toxicity questionnaire.171,172 The
return to work, lower severity of injury/illness, return to work coordi- downstream impact of financial toxicity on patients with cancer is signifi-
nation, and multidisciplinary interventions that include the workplace cant, as increased levels of financial toxicity are associated with decreased
and stakeholders. On the other hand, factors associated with negative adherence to cancer treatment, increased symptom burden, decreased
return-to-work outcomes were advanced age, female gender, higher QOL, higher unmet needs for HNC survivors, and decreased survival.173–
177
pain or disability, depression, higher physical work demands, previous Financial toxicity is also a common problem for HNC caregivers and
sick leave and unemployment, and activity limitations.163 one that can have a devastating impact.152,155
It is important for physicians caring for HNC patients to understand Although many sociodemographic determinants of financial toxic-
medical disability and the protections afforded by the United States law. ity are beyond the control of the multidisciplinary HNC team, pro-
When employees are injured or disabled or become ill on the job, they viders can help by increasing awareness that financial toxicity is
may be entitled to medical and/or disability-related leave under two fed- common following treatment for HNC, identifying at-risk patients,
eral laws: the Americans with Disabilities Act (ADA) and the Family and alerting patients and caregiver to resources for its management, and
Medical Leave Act (FMLA). An individual with a disability is defined as a making referrals to social workers and financial navigators who may
person who: (1) has physical or mental impairment that substantially further facilitate engagement with social welfare systems to help
limits one or more major life activities; (2) has a record of such an impair- assess and manage HNC-related financial toxicity.152,166
ment; or (3) is regarded as having such an impairment.164 The ADA does
not specifically require employers to provide medical or disability-related
leave. However, it does require employers to make reasonable accom- 3.12.1 | Recommendation
modations for qualified employees with disabilities if necessary to per-
form essential job functions or to benefit from the same opportunities Patients who have undergone treatment for HNC:
164
and rights afforded employees without disabilities. Accommodations
can include modifications to work schedules (e.g., 8-h shifts instead of a. Can be referred to social workers and financial navigators by their
12-h shifts or 5-day work week, no overtime), restricted duties (i.e., limi- survivorship team to navigate health care costs associated with
tations on lifting), or medical leave.164 HNC care (Oxford Category 5).
Patients who have undergone treatment for HNC should be: 4.1 | Primary care physician
a. Counseled by their survivorship team on medical disability rights PCPs have a critical and continuing role in the management of acute
and protections afforded by federal law (Oxford Category 5). and chronic care of HNC survivors, supporting the diagnosis and
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
84 GOYAL ET AL.
management of HNC, and promoting good health behaviors. It is criti- demineralization/caries, periodontal status, oral hygiene, changes due
cal that the oncology team communicate regularly with the PCP. A to tissue fibrosis (tongue mobility, presence of trismus, oral aperture),
treatment summary, risk of recurrence, short-term and long-term local infection, and exposed bone. Diet and nutritional status should
effects of treatment, and an individualized surveillance/survivorship also be assessed. Dental prophylaxis should include brushing with
plan should be available to PCP and HNC providers. Several docu- remineralizing toothpaste, dental floss utilization, and fluoride supple-
ments exist to help communicate this information including those mentation. Consultation with the oncology team and review of the
6,7
published by AHNS and ASCO. Of note, the use of a standardized radiation fields are indicated prior to any invasive dental treatment is
survivorship care plan has been integrated into the 2020 Commission performed. Although there is limited evidence, consideration may be
on Cancer Standards for member organizations (Standard 4.8).160 given to hyperbaric oxygen therapy in HNC patients with a prior his-
PCPs should be aware of the signs, symptoms, and physical find- tory of radiotherapy who require dental extractions.187 Following this,
ings of cancer recurrence or second malignancy and promptly refer patient management and referral for oral and dental care can be per-
patients back to the oncology team for further investigation of any formed as deemed appropriate. A recent study reported only 50% of
suspicious findings. The PCP should engage in discussion and counsel- HNC survivors received recommended post-treatment oral/dental
ing regarding cardiovascular health, smoking cessation, alcohol con- care, which further highlights the need for a more coordinated and
sumption, diet/nutrition/weight, regular physical activity, dental enhanced multidisciplinary approach in educating and helping patients
hygiene, and mental/psychosocial health. General well-being and utilize oral/dental supportive care.188
QOL should be assessed including weight, energy/fatigue, mood
(depression), sleep, activity (work, avocation). As HNC survivors are at
an increased risk of developing second primary malignancies, both in 4.2.1 | Recommendation
head and neck and non-head and neck sites, the PCP should also per-
form age-appropriate and gender-appropriate screening of HNC survi- Patients who have undergone treatment for HNC:
vors for other neoplasms, as they would for patients in the general
population.178–181 The multidisciplinary cancer team and/or PCP a. Should be counseled by their survivorship team to maintain close
should also routinely evaluate thyroid function by measuring TSH/T4 follow-up with a dental professional (Oxford Category 1B).
every 6–12 months in patients with a surgically compromised thyroid b. Can be encouraged by their survivorship team to avoid tobacco
gland or history of neck irradiation.182–184 and alcohol to minimize the risk of dental disease (Oxford
Category 5).
4.1.1 | Recommendation
4.3 | Substance abuse
Patients who have undergone treatment for HNC should be:
According to pooled analyses of United States HNC cohorts
a. Followed by their PCP for age-appropriate and gender-appropriate (n = 7570, 1981–2006), 58% of HNC survivors were current smokers
screening of other neoplasms, general health, and well-being at diagnosis and 37% reported consuming >3 alcoholic beverages per
(Oxford Category 2A). day.189 Over 50% of HNC survivors continue smoking after diagnosis
and persistent tobacco or alcohol dependence has been associated
with an increased risk of perioperative complications, recurrence, sec-
4.2 | Dental care ond primary cancers, and mortality in HNC survivors.190–196 An esti-
mated 10% of HNC survivors report ever using marijuana.197 While
HNC survivors experience a wide range of changes that increase their studies have not identified a clear association between marijuana and
risk of oral and dental diseases.185,186 Dental providers have a role in HNC, some have reported an association with oropharyngeal squa-
oral and dental care from diagnosis to survivorship of HNC patients, mous cell carcinoma (OPSCC).196,197 Approximately 10% of HNC sur-
establishing oral health and preventive programs, and manage HNC vivors exhibit new opioid dependence 6 months after treatment. In
treatment complications. A comprehensive history and physical exam- the general population, opioid use disorder, defined as a problematic
ination, including issues related to primary cancer treatment and pattern of utilizing opioids that leads to significant distress or impair-
potential survivorship symptoms, should be addressed at each dental ment over 12 months, is associated with increased mortality from
visit. An understanding of prior cancer therapy, especially radiation accidental overdose, trauma, suicide, or infectious disease.65,67,198
dose and treatment fields, is required. The frequency of dental visits Evidence demonstrating that directed tobacco or alcohol treatment in
should be individualized, often requiring more frequent visits. At each HNC patients yields improved abstinence rates compared to usual
visit, the history should address head and neck, oral/dental symptoms, care is limited and underpowered.199–201 Hence, guideline recommen-
tobacco/alcohol cessation, and surveillance for potential recurrence dations for HNC and other cancer patients are inferred from data con-
or second primary cancers. Symptoms include sensory changes (pain, firming the efficacy of treatment in adults generally.202,203 Timely
taste), xerostomia, and dysphagia. Oral and dental evaluation should management of tobacco or alcohol dependence before oncologic
focus on mucosal and gingival integrity, oral hydration, dental treatment is preferred and may associate most strongly with reduced
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
GOYAL ET AL. 85
phonation will also need to keep the prosthesis clean of crusting and a. Counseled by their survivorship team on the sequelae of HPV-
debris with a bristle brush. Should the tracheoesophageal prosthesis related oncologic disease as well as the clinical evidence relating to
become incompetent, it will start leaking esophageal contents into the the benefits of HPV vaccine (Oxford Category 5).
airway, resulting in frank aspiration and mandating replacement. Some
patients may require routine use of a “laryngectomy tube” to maintain
stoma patency and minimize stomal stenosis; these stents should also 5 | CONC LU SION
219
be removed and cleaned of crusting and debris regularly.
Cancer survivorship necessarily incorporates a multidisciplinary
approach centered around the patient and the caregiver, led by oncol-
4.5.3 | Recommendation ogists (surgical, medical, and radiation) and primary care providers and
managed by a wide variety of allied health providers including but not
Patients who have undergone treatment for HNC should be: limited to therapists (speech, physical, occupational, and respiratory),
dieticians, social workers, dentists, and psycho-oncologists. With
a. Educated in the tracheostomy and laryngectomy stoma care if increasing survival related to HNC treatment, addressing post-treat-
either is present by their survivorship team (Oxford Category 5). ment concerns will have a profound impact on patient quality of life
and survival. There continues to be a need to define effective and effi-
cient programs that can coordinate this multidisciplinary effort toward
4.6 | HPV counseling survivorship.
The incidence of HPV-associated OPSCC is rising; the disease now ACKNOWLEDG MENTS
comprises 70% of OPSCC in the United States. Despite this, there is a The authors would like to acknowledge Jenna Loewus and Isabella
significant gap in knowledge and awareness about HPV and HPV- Yeung for administrative support.
associated OPSCC among both general adults and HPV OPSCC survi-
vors.221–225 HPV OPSCC survivors report reduced sexual activity,53 CONFLIC T OF INT ER E ST
informational, emotional, and psychosocial needs related to their diag- None of the authors have any conflicts of interest.
nosis including self-blame, guilt, anxiety, distress, and concern about
transmitting HPV to others.224–226 Broad patient information needs OR CID
may include knowledge regarding: the prevalence, nature, and trans- Neerav Goyal https://orcid.org/0000-0001-7783-1097
mission of HPV infection, risk to current and future partners, and util- Andrew Day https://orcid.org/0000-0001-7187-4125
ity of preventative vaccination. Recent publications have provided Evan Graboyes https://orcid.org/0000-0003-3766-468X
227,228
helpful resources for both clinicians and patients. To better Vlad Sandulache https://orcid.org/0000-0002-9205-385X
understand general knowledge and advocacy intent, a cross-sectional Amy M. Williams https://orcid.org/0000-0001-9643-3684
study (n = 200) of HPV-related cancer survivors (i.e., cervical, vaginal, Cherie-Ann Nathan https://orcid.org/0000-0001-7386-318X
vulvar, penile, anal, or oropharyngeal) revealed only 33% of respon-
dents were aware that their cancer was HPV-associated and 57% RE FE RE NCE S
reported that the HPV vaccine is safe. Of those participants who 1. Siegel RL, Miller KD, Goding Sauer A, et al. Colorectal cancer statis-
understood that their cancer was HPV-related, they were significantly tics, 2020. CA Cancer J Clin. 2020;70(3):145-164.
2. National Comprehensive Cancer Network. Head and neck cancer.
more likely to have their children vaccinated, recommend the HPV
2020. https://www.nccn.org/professionals/physician_gls/pdf/head-
vaccine, serve as a peer mentor for HPV-related cancer patients, and and-neck.pdf
advocate for increasing vaccination rates. Raising awareness for HPV- 3. Chaturvedi AK, Engels EA, Pfeiffer RM, et al. Human papillomavirus
related cancer allows for the empowerment of survivors, which results and rising oropharyngeal cancer incidence in the United States. J Clin
Oncol. 2011;29(32):4294-4301.
in the development of key opinion leaders in the realm of HPV vac-
4. Patel MA, Blackford AL, Rettig EM, Richmon JD, Eisele DW,
cine advocacy.229 Thus, clinicians should routinely attend to the infor- Fakhry C. Rising population of survivors of oral squamous cell cancer
mational needs of HPV-associated OPSCC patients and survivors as in the United States. Cancer. 2016;122(9):1380-1387.
well as offer treatment or referral for the emotional, psychosocial, or 5. Mullan F. Seasons of survival: reflections of a physician with cancer.
N Engl J Med. 1985;313(4):270-273.
sexual needs of HPV OPSCC survivors.230–232 Further evaluation of
6. Miller MC, Shuman AG, American Head and Neck Society's Com-
HPV counseling implementation into routine care and corollary out- mittee on Survivorship. Survivorship in head and neck cancer: a
comes will be needed. primer. JAMA Otolaryngol Head Neck Surg. 2016;142(10):1002-
1008.
7. Cohen EE, LaMonte SJ, Erb NL, et al. American Cancer Society head
and neck cancer survivorship care guideline. CA Cancer J Clin. 2016;
4.6.1 | Recommendation 66(3):203-239.
8. Nekhlyudov L, Lacchetti C, Davis NB, et al. Head and neck cancer
Patients who have undergone treatment for HPV OPSCC should be: survivorship care guideline: American Society of Clinical Oncology
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
GOYAL ET AL. 87
clinical practice guideline endorsement of the American Cancer Soci- 27. Osazuwa-Peters N, Simpson MC, Zhao L, et al. Suicide risk among
ety guideline. J Clin Oncol. 2017;35(14):1606-1621. cancer survivors: head and neck versus other cancers. Cancer. 2018;
9. Ball C, Sackett D, Phillips B, Haynes B, Straus S. Oxford Centre for 124(20):4072-4079.
evidence-based medicine – levels of evidence. 2009. Accessed Feb- 28. Massa ST, Rohde RL, McKinstry C, et al. An assessment of patient
ruary 4, 2020. https://www.cebm.net/2009/06/oxford-centre- burdens from head and neck cancer survivorship care. Oral Oncol.
evidence-based-medicine-levels-evidence-march-2009/ 2018;82:115-121.
10. Brennan KE, Hall SF, Owen TE, Griffiths RJ, Peng Y. Variation in rou- 29. Monterosso L, Platt V, Bulsara M, Berg M. Systematic review and
tine follow-up care after curative treatment for head-and-neck can- meta-analysis of patient reported outcomes for nurse-led models of
cer: a population-based study in Ontario. Curr Oncol. 2018;25(2): survivorship care for adult cancer patients. Cancer Treat Rev. 2019;
e120-e131. 73:62-72.
11. Watanabe A, Hosokawa M, Taniguchi M, Sasaki S. Periodic pha- 30. Thom B, Boekhout AH, Corcoran S, Adsuar R, Oeffinger KC,
ryngolaryngoscopy detects early head and neck cancer and improves McCabe MS. Advanced practice providers and survivorship care:
survival in esophageal cancer. Ann Thorac Surg. 2003;76(5):1699- they can deliver. J Oncol Pract. 2019;15(3):e230-e237.
1705. 31. Absolom K, Eiser C, Michel G, et al. Follow-up care for cancer sur-
12. Zhou H, Zhang J, Guo L, Nie J, Zhu C, Ma X. The value of narrow vivors: views of the younger adult. Br J Cancer. 2009;101(4):
band imaging in diagnosis of head and neck cancer: a meta-analysis. 561-567.
Sci Rep. 2018;8(1):515. 32. Brennan ME, Butow P, Marven M, Spillane AJ, Boyle FM. Survivor-
13. Siddiqui F, Movsas B. Management of radiation toxicity in head and ship care after breast cancer treatment – experiences and prefer-
neck cancers. Semin Radiat Oncol. 2017;27(4):340-349. ences of Australian women. Breast. 2011;20(3):271-277.
14. Galloway TA, Robert J. Management and prevention of complica- 33. Cancer Survivorship Algorithms. MD Anderson Cancer Center.
tions during initial treatment of head and neck cancer. 2020. Accessed December 1, 2020. https://www.mdanderson.org/for-
https://www.uptodate.com/contents/management-and-prevention- physicians/clinical-tools-resources/clinical-practice-algorithms/
of-complications-during-initial-treatment-of-head-and-neck-cancer survivorship-algorithms.html
15. Seretny M, Currie GL, Sena ES, et al. Incidence, prevalence, and pre- 34. Wall LR, Ward EC, Cartmill B, Hill AJ. Physiological changes to the
dictors of chemotherapy-induced peripheral neuropathy: a system- swallowing mechanism following (chemo)radiotherapy for head and
atic review and meta-analysis. Pain. 2014;155(12):2461-2470. neck cancer: a systematic review. Dysphagia. 2013;28(4):481-493.
16. Staff NP, Grisold A, Grisold W, Windebank AJ. Chemotherapy- 35. Lin YS, Jen YM, Lin JC. Radiation-related cranial nerve palsy in
induced peripheral neuropathy: a current review. Ann Neurol. 2017; patients with nasopharyngeal carcinoma. Cancer. 2002;95(2):
81(6):772-781. 404-409.
17. Smith EM, Pang H, Cirrincione C, et al. Effect of duloxetine on pain, 36. Gillespie MB, Brodsky MB, Day TA, Lee FS, Martin-Harris B.
function, and quality of life among patients with chemotherapy- Swallowing-related quality of life after head and neck cancer treat-
induced painful peripheral neuropathy: a randomized clinical trial. ment. Laryngoscope. 2004;114(8):1362-1367.
JAMA. 2013;309(13):1359-1367. 37. Hutcheson KA, Nurgalieva Z, Zhao H, et al. Two-year prevalence of
18. Fallon MT, Storey DJ, Krishan A, Weir CJ, Mitchell R, Fleetwood- dysphagia and related outcomes in head and neck cancer survivors:
Walker SM, Scott AC, Colvin LA. Cancer treatment-related neuro- an updated SEER-Medicare analysis. Head Neck. 2019;41(2):
pathic pain: proof of concept study with menthol—a TRPM8 agonist. 479-487.
Supportive Care in Cancer. 2015;23:(9):2769-2777. https://doi.org/ 38. Garcia-Peris P, Paron L, Velasco C, et al. Long-term prevalence of
10.1007/s00520-015-2642-8 oropharyngeal dysphagia in head and neck cancer patients: impact
19. Anand P, Elsafa E, Privitera R, et al. Rational treatment of chemo- on quality of life. Clin Nutr. 2007;26(6):710-717.
therapy-induced peripheral neuropathy with capsaicin 8% patch: 39. Hutcheson KA, Barringer DA, Rosenthal DI, May AH, Roberts DB,
from pain relief towards disease modification. J Pain Res. 2019;12: Lewin JS. Swallowing outcomes after radiotherapy for laryngeal car-
2039-2052. cinoma. Arch Otolaryngol Head Neck Surg. 2008;134(2):178-183.
20. Duregon F, Vendramin B, Bullo V, et al. Effects of exercise on cancer 40. Maurer J, Hipp M, Schafer C, Dysphagia KO. Impact on quality of life
patients suffering chemotherapy-induced peripheral neuropathy after radio(chemo)therapy of head and neck cancer. Strahlenther
undergoing treatment: a systematic review. Crit Rev Oncol Hematol. Onkol. 2011;187(11):744-749.
2018;121:90-100. 41. Clarke P, Radford K, Coffey M, Stewart M. Speech and swallow
21. Sacco AGCC, Sanghvi P, et al. Development of care pathways to rehabilitation in head and neck cancer: United Kingdom National
standardize and optimally integrate multidisciplinary care for head Multidisciplinary Guidelines. J Laryngol Otol. 2016;130(suppl 2):
and neck cancer. Oncol Issues. 2018;33(6):28-44. S176-S180.
22. Taplin SH, Clauser S, Rodgers AB, Breslau E, Rayson D. Interfaces 42. Pauloski BR, Rademaker AW, Logemann JA, et al. Pretreatment
across the cancer continuum offer opportunities to improve the pro- swallowing function in patients with head and neck cancer. Head
cess of care. J Natl Cancer Inst Monogr. 2010;2010(40):104-110. Neck. 2000;22(5):474-482.
23. Ng SP, Pollard C 3rd, Berends J, et al. Usefulness of surveillance 43. Kotz T, Federman AD, Kao J, et al. Prophylactic swallowing exercises
imaging in patients with head and neck cancer who are treated with in patients with head and neck cancer undergoing chemoradiation: a
definitive radiotherapy. Cancer. 2019;125(11):1823-1829. randomized trial. Arch Otolaryngol Head Neck Surg. 2012;138(4):
24. Ward MC, Lee NY, Caudell JJ, et al. A competing risk nomogram to 376-382.
predict severe late toxicity after modern re-irradiation for squamous 44. Carnaby-Mann G, Crary MA, Schmalfuss I, Amdur R. “Pharyngocise”:
carcinoma of the head and neck. Oral Oncol. 2019;90:80-86. randomized controlled trial of preventative exercises to maintain
25. Chen MC, Kuan FC, Huang SF, et al. Accelerated risk of premature muscle structure and swallowing function during head-and-neck
ischemic stroke in 5-year survivors of nasopharyngeal carcinoma. chemoradiotherapy. Int J Radiat Oncol Biol Phys. 2012;83(1):
Oncologist. 2019;24(9):e891-e897. 210-219.
26. Eytan DF, Blackford AL, Eisele DW, Fakhry C. Prevalence of com- 45. Hutcheson KA, Bhayani MK, Beadle BM, et al. Eat and exercise dur-
orbidities and effect on survival in survivors of human papillomavi- ing radiotherapy or chemoradiotherapy for pharyngeal cancers: use
rus-related and human papillomavirus-unrelated head and neck it or lose it. JAMA Otolaryngol Head Neck Surg. 2013;139(11):1127-
cancer in the United States. Cancer. 2019;125(2):249-260. 1134.
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
88 GOYAL ET AL.
46. Langmore SE. Normal swallowing: the endoscopic perspective. Endo- 66. Silver N, Dourado J, Hitchcock K, et al. Chronic opioid use in
scopic Evaluation and Treatment of Swallowing Disorders, pp. 37–37; patients undergoing treatment for oropharyngeal cancer. Laryngo-
Thieme Medical Publishers, Incorporated; 2000. scope. 2019;129(9):2087-2093.
47. National Comprehensive Cancer Network. NCCN guidelines version 67. McDermott JD, Eguchi M, Stokes WA, et al. Short- and long-term
1.2019. Cancer-related fatigue. Accessed May 30, 2019. https:// opioid use in patients with oral and oropharynx cancer. Otolaryngol
www.nccn.org/professionals/physician_gls/pdf/fatigue.pdf Head Neck Surg. 2019;160(3):409-419.
48. Spratt DE, Sakae M, Riaz N, et al. Time course and predictors for can- 68. Pang J, Tringale KR, Tapia VJ, et al. Chronic opioid use following sur-
cer-related fatigue in a series of oropharyngeal cancer patients treated gery for oral cavity cancer. JAMA Otolaryngol Head Neck Surg. 2017;
with chemoradiation therapy. Oncologist. 2012;17(4):569-576. 143(12):1187-1194.
49. Jereczek-Fossa BA, Santoro L, Alterio D, et al. Fatigue during head- 69. Sanders JG, Dawes PJ. Gabapentin for perioperative analgesia in
and-neck radiotherapy: prospective study on 117 consecutive otorhinolaryngology-head and neck surgery: systematic review.
patients. Int J Radiat Oncol Biol Phys. 2007;68(2):403-415. Otolaryngol Head Neck Surg. 2016;155(6):893-903.
50. Bower JE, Bak K, Berger A, et al. Screening, assessment, and man- 70. Bar AV, Weinstein G, Dutta PR, Chalian A, Both S, Quon H.
agement of fatigue in adult survivors of cancer: an American Society Gabapentin for the treatment of pain related to radiation-induced
of Clinical oncology clinical practice guideline adaptation. J Clin mucositis in patients with head and neck tumors treated with
Oncol. 2014;32(17):1840-1850. intensity-modulated radiation therapy. Head Neck. 2010;32(2):
51. Rock CL, Doyle C, Demark-Wahnefried W, et al. Nutrition and phys- 173-177.
ical activity guidelines for cancer survivors. CA Cancer J Clin. 2012; 71. Bar AV. Gabapentin for the treatment of cancer-related pain syn-
62(4):243-274. dromes. Rev Recent Clin Trials. 2010;5(3):174-178.
52. Gielissen MF, Verhagen CA, Bleijenberg G. Cognitive behaviour 72. Binczak M, Navez M, Perrichon C, et al. Management of somatic
therapy for fatigued cancer survivors: long-term follow-up. Br J Can- pain induced by head-and-neck cancer treatment: definition and
cer. 2007;97(5):612-618. assessment. Guidelines of the French Oto-Rhino-Laryngology-Head
53. Taberna M, Inglehart RC, Pickard RK, et al. Significant changes in and Neck Surgery Society (SFORL). Eur Ann Otorhinolaryngol Head
sexual behavior after a diagnosis of human papillomavirus-positive Neck Dis. 2014;131(4):243-247.
and human papillomavirus-negative oral cancer. Cancer. 2017;123 73. Katz J, Weinrib A, Fashler SR, et al. The Toronto General Hospital
(7):1156-1165. Transitional Pain Service: development and implementation of a
54. Rogers SN, Hazeldine P, O'Brien K, Lowe D, Roe B. How often do multidisciplinary program to prevent chronic postsurgical pain. J Pain
head and neck cancer patients raise concerns related to intimacy Res. 2015;8:695-702.
and sexuality in routine follow-up clinics? Eur Arch Otorhinolaryngol. 74. Robinson M, Ward L, Mehanna H, Paleri V, Winter SC. Provision of
2015;272(1):207-217. physiotherapy rehabilitation following neck dissection in the UK. J
55. Hordern AJ, Street AF. Communicating about patient sexuality and Laryngol Otol. 2018;132(7):624-627.
intimacy after cancer: mismatched expectations and unmet needs. 75. Dijkstra PU, van Wilgen PC, Buijs RP, et al. Incidence of shoulder
Med J Aust. 2007;186(5):224-227. pain after neck dissection: a clinical explorative study for risk factors.
56. Hoole J, Kanatas A, Calvert A, Rogers SN, Smith AB, Mitchell DA. Head Neck. 2001;23(11):947-953.
Validated questionnaires on intimacy in patients who have had can- 76. Weber C, Dommerich S, Pau HW, Kramp B. Limited mouth opening
cer. Br J Oral Maxillofac Surg. 2015;53(7):584-593. after primary therapy of head and neck cancer. Oral Maxillofac Surg.
57. Hoole J, Kanatas AN, Mitchell DA. Psychosexual therapy and educa- 2010;14(3):169-173.
tion in patients treated for cancer of the head and neck. Br J Oral 77. Gane EM, Michaleff ZA, Cottrell MA, et al. Prevalence, incidence,
Maxillofac Surg. 2015;53(7):601-606. and risk factors for shoulder and neck dysfunction after neck dissec-
58. Ratnasingam J, Karim N, Paramasivam SS, et al. Hypothalamic pitui- tion: a systematic review. Eur J Surg Oncol. 2017;43(7):1199-1218.
tary dysfunction amongst nasopharyngeal cancer survivors. Pituitary. 78. Jepsen J, Laursen L, Larsen A, Hagert CG. Manual strength testing in
2015;18(4):448-455. 14 upper limb muscles: a study of inter-rater reliability. Acta Orthop
59. Huang S, Wang X, Hu C, Ying H. Hypothalamic-pituitary-thyroid Scand. 2004;75(4):442-448.
dysfunction induced by intensity-modulated radiotherapy (IMRT) for 79. Fan E, Ciesla ND, Truong AD, Bhoopathi V, Zeger SL, Needham DM.
adult patients with nasopharyngeal carcinoma. Med Oncol. 2013;30 Inter-rater reliability of manual muscle strength testing in ICU survi-
(4):710. vors and simulated patients. Intensive Care Med. 2010;36(6):1038-
60. Cramer JD, Johnson JT, Nilsen ML. Pain in head and neck cancer 1043.
survivors: prevalence, predictors, and quality-of-life impact. 80. Goldstein DP, Ringash J, Bissada E, et al. Evaluation of shoulder dis-
Otolaryngol Head Neck Surg. 2018;159(5):853-858. ability questionnaires used for the assessment of shoulder disability
61. Terkawi AS, Tsang S, Alshehri AS, Mulafikh DS, Alghulikah AA, after neck dissection for head and neck cancer. Head Neck. 2014;36
AlDhahri SF. The burden of chronic pain after major head and neck (10):1453-1458.
tumor therapy. Saudi J Anaesth. 2017;11(suppl 1):S71-S79. 81. McGarvey AC, Chiarelli PE, Osmotherly PG, Hoffman GR. Physio-
62. Ojo B, Genden EM, Teng MS, Milbury K, Misiukiewicz KJ, Badr H. A therapy for accessory nerve shoulder dysfunction following neck
systematic review of head and neck cancer quality of life assessment dissection surgery: a literature review. Head Neck. 2011;33(2):
instruments. Oral Oncol. 2012;48(10):923-937. 274-280.
63. Smit M, Balm AJ, Hilgers FJ, Tan IB. Pain as sign of recurrent disease 82. McGarvey AC, Hoffman GR, Osmotherly PG, Chiarelli PE. Maximiz-
in head and neck squamous cell carcinoma. Head Neck. 2001;23(5): ing shoulder function after accessory nerve injury and neck dissec-
372-375. tion surgery: a multicenter randomized controlled trial. Head Neck.
64. Dowell D, Haegerich TM, Chou R. CDC guideline for prescribing opi- 2015;37(7):1022-1031.
oids for chronic pain – United States. JAMA. 2016;315(15):1624- 83. Kirkpatrick JP, van der Kogel AJ, Schultheiss TE. Radiation dose–vol-
1645. ume effects in the spinal cord. Int J Radiat Oncol Biol Phys. 2010;76
65. Smith WH, Luskin I, Resende Salgado L, et al. Risk of prolonged (3 suppl):S42-S49.
opioid use among cancer patients undergoing curative intent radia- 84. Laidley HM, Noble DJ, Barnett GC, et al. Identifying risk factors for
tion therapy for head and neck malignancies. Oral Oncol. 2019;92: L'Hermitte's sign after IMRT for head and neck cancer. Radiat Oncol.
1-5. 2018;13(1):84.
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
GOYAL ET AL. 89
85. Esik O, Csere T, Stefanits K, et al. A review on radiogenic Lhermitte's 106. Rieke K, Schmid KK, Lydiatt W, Houfek J, Boilesen E, Watanabe-
sign. Pathol Oncol Res. 2003;9(2):115-120. Galloway S. Depression and survival in head and neck cancer
86. Pak D, Vineberg K, Feng F, Ten Haken RK, Eisbruch A. Lhermitte patients. Oral Oncol. 2017;65:76-82.
sign after chemo-IMRT of head-and-neck cancer: incidence, doses, 107. Henry M, Fuehrmann F, Hier M, et al. Contextual and historical fac-
and potential mechanisms. Int J Radiat Oncol Biol Phys. 2012;83(5): tors for increased levels of anxiety and depression in patients with
1528-1533. head and neck cancer: a prospective longitudinal study. Head Neck.
87. Gemici C. Lhermitte's sign: review with special emphasis in oncology 2019;41(8):2538-2548.
practice. Crit Rev Oncol Hematol. 2010;74(2):79-86. 108. Wu YS, Lin PY, Chien CY, et al. Anxiety and depression in patients
88. van der Geer SJ, van Rijn PV, Kamstra JI, Roodenburg JLN, with head and neck cancer: 6-month follow-up study.
Dijkstra PU. Criterion for trismus in head and neck cancer patients: a Neuropsychiatr Dis Treat. 2016;12:1029-1036.
verification study. Support Care Cancer. 2019;27(3):1129-1137. 109. Fingeret MC, Vidrine DJ, Reece GP, Gillenwater AM, Gritz ER. Mul-
89. Pauli N, Johnson J, Finizia C, Andrell P. The incidence of trismus and tidimensional analysis of body image concerns among newly diag-
long-term impact on health-related quality of life in patients with nosed patients with oral cavity cancer. Head Neck. 2010;32(3):
head and neck cancer. Acta Oncol. 2013;52(6):1137-1145. 301-309.
90. van der Geer SJ, van Rijn PV, Kamstra JI, et al. Prevalence and pre- 110. Rhoten BA, Murphy B, Ridner SH. Body image in patients with head
diction of trismus in patients with head and neck cancer: a cross-sec- and neck cancer: a review of the literature. Oral Oncol. 2013;49(8):
tional study. Head Neck. 2019;41(1):64-71. 753-760.
91. Kamstra JI, van Leeuwen M, Roodenburg JL, Dijkstra PU. Exercise 111. Ellis MA, Sterba KR, Day TA, et al. Body image disturbance in surgi-
therapy for trismus secondary to head and neck cancer: a systematic cally treated head and neck cancer patients: a patient-centered
review. Head Neck. 2017;39(1):160-169. approach. Otolaryngol Head Neck Surg. 2019;161(2):278-287.
92. Scherpenhuizen A, van Waes AM, Janssen LM, Van Cann EM, 112. Ellis MA, Sterba KR, Brennan EA, et al. A systematic review of
Stegeman I. The effect of exercise therapy in head and neck cancer patient-reported outcome measures assessing body image distur-
patients in the treatment of radiotherapy-induced trismus: a system- bance in patients with head and neck cancer. Otolaryngol Head Neck
atic review. Oral Oncol. 2015;51(8):745-750. Surg. 2019;160(6):941-954.
93. Dijkstra PU, Kalk WW, Roodenburg JL. Trismus in head and neck 113. Fingeret MC, Teo I, Epner DE. Managing body image difficulties of
oncology: a systematic review. Oral Oncol. 2004;40(9):879-889. adult cancer patients: lessons from available research. Cancer. 2014;
94. Smith BG, Lewin JS. Lymphedema management in head and 120(5):633-641.
neck cancer. Curr Opin Otolaryngol Head Neck Surg. 2010;18(3): 114. Chen SC, Huang BS, Lin CY, et al. Psychosocial effects of a skin cam-
153-158. ouflage program in female survivors with head and neck cancer: a
95. Deng J, Ridner SH, Murphy BA. Lymphedema in patients with head randomized controlled trial. Psychooncology. 2017;26(9):1376-1383.
and neck cancer. Oncol Nurs Forum. 2011;38(1):E1-E10. 115. Huang S, Liu HE. Effectiveness of cosmetic rehabilitation on the
96. Ridner SH, Dietrich MS, Niermann K, Cmelak A, Mannion K, body image of oral cancer patients in Taiwan. Support Care Cancer.
Murphy B. A prospective study of the lymphedema and fibrosis con- 2008;16(9):981-986.
tinuum in patients with head and neck cancer. Lymphat Res Biol. 116. Lydiatt WM, Moran J, Burke WJ. A review of depression in the head
2016;14(4):198-205. and neck cancer patient. Clin Adv Hematol Oncol. 2009;7(6):
97. Klernas P, Johnsson A, Horstmann V, Johansson K. Health-related 397-403.
quality of life in patients with lymphoedema – a cross-sectional 117. Denlinger CS, Sanft T, Baker KS, et al. Survivorship, version 2.2017,
study. Scand J Caring Sci. 2018;32(2):634-644. NCCN clinical practice guidelines in oncology. J Natl Compr Canc
98. Murphy BA, Gilbert J. Dysphagia in head and neck cancer patients Netw. 2017;15(9):1140-1163.
treated with radiation: assessment, sequelae, and rehabilitation. 118. Beck AT, Steer RA. Beck Anxiety Inventory Manual. Psychological
Semin Radiat Oncol. 2009;19(1):35-42. Corporation; 1993.
99. Poulsen MG, Riddle B, Keller J, Porceddu SV, Tripcony L. Predictors 119. Kroenke K, Spitzer RL, Williams JB. The PHQ-9: validity of a brief
of acute grade 4 swallowing toxicity in patients with stages III and IV depression severity measure. J Gen Intern Med. 2001;16(9):606-613.
squamous carcinoma of the head and neck treated with radiother- 120. Chen AM, Daly ME, Vazquez E, et al. Depression among long-term
apy alone. Radiother Oncol. 2008;87(2):253-259. survivors of head and neck cancer treated with radiation therapy.
100. Penner JL. Psychosocial care of patients with head and neck cancer. JAMA Otolaryngol Head Neck Surg. 2013;139(9):885-889.
Semin Oncol Nurs. 2009;25(3):231-241. 121. Lydiatt WM, Bessette D, Schmid KK, Sayles H, Burke WJ. Preven-
101. Yao T, Beadle B, Holsinger CF, Starmer HM. Effectiveness of a tion of depression with escitalopram in patients undergoing treat-
home-based head and neck lymphedema management program: a ment for head and neck cancer: randomized, double-blind, placebo-
pilot study. Laryngoscope. 2020;130:E858-E862. controlled clinical trial. JAMA Otolaryngol Head Neck Surg. 2013;139
102. Smith BG, Hutcheson KA, Little LG, et al. Lymphedema outcomes in (7):678-686.
patients with head and neck cancer. Otolaryngol Head Neck Surg. 122. Jesse MT, Ryan ME, Eshelman A, et al. Integrated psychological care
2015;152(2):284-291. in head and neck cancer: views from health care providers, patients,
103. Fingeret MC, Yuan Y, Urbauer D, Weston J, Nipomnick S, Weber R. and supports. Laryngoscope. 2015;125(6):1345-1351.
The nature and extent of body image concerns among surgically 123. Schou I, Ekeberg O, Karesen R, Sorensen E. Psychosocial interven-
treated patients with head and neck cancer. Psychooncology. 2012; tion as a component of routine breast cancer care – who partici-
21(8):836-844. pates and does it help? Psychooncology. 2008;17(7):716-720.
104. Graboyes EM, Hill EG, Marsh CH, Maurer S, Day TA, Sterba KR. 124. Golant M, Lieberman M, Giese-Davis J, Winzelberg A, Ellis W.
Body image disturbance in surgically treated head and neck cancer Emotional expression and facilitation of online vs. face-to-face
patients: a prospective cohort pilot study. Otolaryngol Head Neck breast cancer support groups. Psychooncology. 2004;13(1):
Surg. 2019;161(1):105-110. S18-S19.
105. Fingeret MC, Hutcheson KA, Jensen K, Yuan Y, Urbauer D, 125. Algtewi EE, Owens J, Baker SR. Analysing people with head and
Lewin JS. Associations among speech, eating, and body image con- neck cancers’ use of online support groups. Cyberpsychology: Journal
cerns for surgical patients with head and neck cancer. Head Neck. of Psychosocial Research on Cyberspace. 2015;9:(4). https://doi.org/
2013;35(3):354-360. 10.5817/cp2015-4-6
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
90 GOYAL ET AL.
126. Zeller JL. High suicide risk found for patients with head and neck 146. Balfe M, O'Brien KM, Timmons A, et al. Informal caregiving in head
cancer. JAMA. 2006;296(14):1716-1717. and neck cancer: caregiving activities and psychological well-being.
127. Henry M, Rosberger Z, Bertrand L, et al. Prevalence and risk fac- Eur J Cancer Care (Engl). 2018;27(2):e12520.
tors of suicidal ideation among patients with head and neck can- 147. Chen SC, Lai YH, Liao CT, et al. Unmet supportive care needs and
cer: longitudinal study. Otolaryngol Head Neck Surg. 2018;159(5): characteristics of family caregivers of patients with oral cancer after
843-852. surgery. Psychooncology. 2014;23(5):569-577.
128. Kam D, Salib A, Gorgy G, et al. Incidence of suicide in patients with 148. Longacre ML, Galloway TJ, Parvanta CF, Fang CY. Medical commu-
head and neck cancer. JAMA Otolaryngol Head Neck Surg. 2015;141 nication-related informational need and resource preferences
(12):1075-1081. among family caregivers for head and neck cancer patients. J Cancer
129. Nader ME, Gidley PW. Challenges of hearing rehabilitation after Educ. 2015;30(4):786-791.
radiation and chemotherapy. J Neurol Surg B Skull Base. 2019;80(2): 149. Penner JL, McClement S, Lobchuk M, Daeninck P. Family members'
214-224. experiences caring for patients with advanced head and neck cancer
130. Bhandare N, Antonelli PJ, Morris CG, Malayapa RS, receiving tube feeding: a descriptive phenomenological study. J Pain
Mendenhall WM. Ototoxicity after radiotherapy for head and neck Symptom Manage. 2012;44(4):563-571.
tumors. Int J Radiat Oncol Biol Phys. 2007;67(2):469-479. 150. Sterba KR, Zapka J, Armeson KE, et al. Physical and emotional well-
131. Strojan P, Hutcheson KA, Eisbruch A, et al. Treatment of late being and support in newly diagnosed head and neck cancer
sequelae after radiotherapy for head and neck cancer. Cancer Treat patient–caregiver dyads. J Psychosoc Oncol. 2017;35(6):646-665.
Rev. 2017;59:79-92. 151. Badr H, Herbert K, Reckson B, Rainey H, Sallam A, Gupta V. Unmet
132. Zuur CL, Simis YJ, Lamers EA, et al. Risk factors for hearing loss in needs and relationship challenges of head and neck cancer patients
patients treated with intensity-modulated radiotherapy for head- and their spouses. J Psychosoc Oncol. 2016;34(4):336-346.
and-neck tumors. Int J Radiat Oncol Biol Phys. 2009;74(2): 152. Balfe M, Butow P, O'Sullivan E, Gooberman-Hill R, Timmons A,
490-496. Sharp L. The financial impact of head and neck cancer caregiving: a
133. Hitchcock YJ, Tward JD, Szabo A, Bentz BG, Shrieve DC. Relative qualitative study. Psychooncology. 2016;25(12):1441-1447.
contributions of radiation and cisplatin-based chemotherapy to sen- 153. Verdonck-de Leeuw IM, Eerenstein SE, Van der Linden MH,
sorineural hearing loss in head-and-neck cancer patients. Int J Radiat Kuik DJ, de Bree R, Leemans CR. Distress in spouses and patients
Oncol Biol Phys. 2009;73(3):779-788. after treatment for head and neck cancer. Laryngoscope. 2007;117
134. McDowell LJ, Rock K, Xu W, et al. Long-term late toxicity, quality of (2):238-241.
life, and emotional distress in patients with nasopharyngeal carci- 154. Castellanos EH, Dietrich MS, Bond SM, et al. Impact of patient
noma treated with intensity modulated radiation therapy. Int J symptoms and caregiving tasks on psychological distress in care-
Radiat Oncol Biol Phys. 2018;102(2):340-352. givers for head and neck cancer (HNC). Psychooncology. 2019;28(3):
135. Wakisaka H, Yamada H, Motoyoshi K, Ugumori T, Takahashi H, 511-517.
Hyodo M. Incidence of long-term ipsilateral and contralateral oto- 155. Giuliani M, Milne R, McQuestion M, et al. Partner's survivorship care
toxicity following radiotherapy for nasopharyngeal carcinoma. Auris needs: an analysis in head and neck cancer patients. Oral Oncol.
Nasus Larynx. 2011;38(1):95-100. 2017;71:113-121.
136. Cianfrone G, Pentangelo D, Cianfrone F, et al. Pharmacological 156. Sterba KR, Zapka J, LaPelle N, et al. Development of a survivorship
drugs inducing ototoxicity, vestibular symptoms and tinnitus: a rea- needs assessment planning tool for head and neck cancer survivors
soned and updated guide. Eur Rev Med Pharmacol Sci. 2011;15(6): and their caregivers: a preliminary study. J Cancer Surviv. 2017;11(6):
601-636. 822-832.
137. Dille MF, Ellingson RM, McMillan GP, Konrad-Martin D. ABR 157. Sterba KR, Armeson K, Zapka J, et al. Evaluation of a survivorship
obtained from time-efficient train stimuli for cisplatin ototoxicity needs assessment planning tool for head and neck cancer survivor–
monitoring. J Am Acad Audiol. 2013;24(9):769-781. caregiver dyads. J Cancer Surviv. 2019;13(1):117-129.
138. Sun DQ, Ward BK, Semenov YR, Carey JP, Della Santina CC. Bilat- 158. Badr H, Lipnick D, Diefenbach MA, et al. Development and usability
eral vestibular deficiency: quality of life and economic implications. testing of a web-based self-management intervention for oral can-
JAMA Otolaryngol Head Neck Surg. 2014;140(6):527-534. cer survivors and their family caregivers. Eur J Cancer Care (Engl).
139. Frisina RD, Wheeler HE, Fossa SD, et al. Comprehensive audiomet- 2016;25(5):806-821.
ric analysis of hearing impairment and tinnitus after cisplatin-based 159. Badr H, Krebs P. A systematic review and meta-analysis of psycho-
chemotherapy in survivors of adult-onset cancer. J Clin Oncol. 2016; social interventions for couples coping with cancer. Psychooncology.
34(23):2712-2720. 2013;22(8):1688-1704.
140. Longacre ML, Ridge JA, Burtness BA, Galloway TJ, Fang CY. Psycho- 160. American College of Surgeons. Commission on Cancer's (CoC) Cancer
logical functioning of caregivers for head and neck cancer patients. Program Standards: Ensuring Patient-Centered Care (2020 Edition).
Oral Oncol. 2012;48(1):18-25. https://www.facs.org/quality-programs/cancer/coc/standards/2020
141. Sterba KR, Zapka J, Cranos C, Laursen A, Day TA. Quality of life in 161. Schapira L. Why Peer Support is Important for People Coping with Can-
head and neck cancer patient–caregiver dyads: a systematic review. cer. Vol 2020. Cancer.Net; 2017.
Cancer Nurs. 2016;39(3):238-250. 162. Huber J, Muck T, Maatz P, et al. Face-to-face vs. online peer support
142. Bond SM, Schumacher K, Sherrod A, et al. Development of the head groups for prostate cancer: a cross-sectional comparison study. J
and neck cancer caregiving task inventory. Eur J Oncol Nurs. 2016; Cancer Surviv. 2018;12(1):1-9.
24:29-38. 163. Cancelliere C, Donovan J, Stochkendahl MJ, et al. Factors affecting
143. Murphy BA, Deng J. Advances in supportive care for late effects of return to work after injury or illness: best evidence synthesis of sys-
head and neck cancer. J Clin Oncol. 2015;33(29):3314-3321. tematic reviews. Chiropr Man Ther. 2016;24(1):32.
144. Murphy BA, Ridner S, Wells N, Dietrich M. Quality of life research in 164. Office of Disability Employment Policy–United States Department
head and neck cancer: a review of the current state of the science. of Labor. Department of Labor.
Crit Rev Oncol Hematol. 2007;62(3):251-267. 165. Massa ST, Osazuwa-Peters N, Adjei Boakye E, Walker RJ,
145. Ringash J, Bernstein LJ, Devins G, et al. Head and neck cancer survi- Ward GM. Comparison of the financial burden of survivors of head
vorship: learning the needs, meeting the needs. Semin Radiat Oncol. and neck cancer with other cancer survivors. JAMA Otolaryngol Head
2018;28(1):64-74. Neck Surg. 2019;145(3):239-249.
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
GOYAL ET AL. 91
166. Deschler DG. Head and neck cancer compared with other cancers – 187. Chuang SK. Limited evidence to demonstrate that the use of
does the great equalizer equalize equally? JAMA Otolaryngol Head hyperbaric oxygen (HBO) therapy reduces the incidence of
Neck Surg. 2019;145(3):249-250. osteoradionecrosis in irradiated patients requiring tooth extraction.
167. Zafar SY, Abernethy AP. Financial toxicity, part I: a new name for a J Evid Based Dent Pract. 2012;12(3 suppl):248-250.
growing problem. Oncology (Williston Park). 2013;27(2):80-149. 188. Epstein JB, Smith DK, Villines D, et al. Patterns of oral and dental
168. Altice CK, Banegas MP, Tucker-Seeley RD, Yabroff KR. Financial care education and utilization in head and neck cancer patients. Sup-
hardships experienced by cancer survivors: a systematic review. J port Care Cancer. 2018;26(8):2591-2603.
Natl Cancer Inst. 2017;109(2):djw205. 189. Voltzke KJ, Lee YA, Zhang ZF, et al. Racial differences in the rela-
169. Krouse JH, Krouse HJ, Fabian RL. Adaptation to surgery for head tionship between tobacco, alcohol, and the risk of head and neck
and neck cancer. Laryngoscope. 1989;99(8 Pt 1):789-794. cancer: pooled analysis of US studies in the INHANCE Consortium.
170. de Souza JA, Kung S, O'Connor J, Yap BJ. Determinants of patient- Cancer Causes Control. 2018;29(7):619-630.
centered financial stress in patients with locally advanced head and 190. Burris JL, Studts JL, DeRosa AP, Ostroff JS. Systematic review of
neck cancer. J Oncol Pract. 2017;13(4):e310-e318. tobacco use after lung or head/neck cancer diagnosis: results and
171. Banthin JS, Cunningham P, Bernard DM. Financial burden of health recommendations for future research. Cancer Epidemiol Biomarkers
care, 2001–2004. Health Aff (Millwood). 2008;27(1):188-195. Prev. 2015;24(10):1450-1461.
172. de Souza JA, Yap BJ, Hlubocky FJ, et al. The development of a finan- 191. Shields PG, Herbst RS, Arenberg D, et al. Smoking cessation, version
cial toxicity patient-reported outcome in cancer: the COST measure. 1.2016, NCCN clinical practice guidelines in oncology. J Natl Compr
Cancer. 2014;120(20):3245-3253. Canc Netw. 2016;14(11):1430-1468.
173. Neugut AI, Subar M, Wilde ET, et al. Association between prescrip- 192. Densky J, Eskander A, Kang S, et al. Risk factors associated with
tion co-payment amount and compliance with adjuvant hormonal postoperative delirium in patients undergoing head and neck free
therapy in women with early-stage breast cancer. J Clin Oncol. 2011; flap reconstruction. JAMA Otolaryngol Head Neck Surg. 2019;145(3):
29(18):2534-2542. 216-221.
174. Lathan CS, Cronin A, Tucker-Seeley R, Zafar SY, Ayanian JZ, 193. Browman GP, Wong G, Hodson I, et al. Influence of cigarette
Schrag D. Association of financial strain with symptom burden and smoking on the efficacy of radiation therapy in head and neck can-
quality of life for patients with lung or colorectal cancer. J Clin Oncol. cer. N Engl J Med. 1993;328(3):159-163.
2016;34(15):1732-1740. 194. Day GL, Blot WJ, Shore RE, et al. Second cancers following oral and
175. Zafar SY, McNeil RB, Thomas CM, Lathan CS, Ayanian JZ, pharyngeal cancers: role of tobacco and alcohol. J Natl Cancer Inst.
Provenzale D. Population-based assessment of cancer survivors' 1994;86(2):131-137.
financial burden and quality of life: a prospective cohort study. J 195. Deleyiannis FW, Thomas DB, Vaughan TL, Davis S. Alcoholism:
Oncol Pract. 2015;11(2):145-150. independent predictor of survival in patients with head and neck
176. O'Brien KM, Timmons A, Butow P, et al. Associations between cancer. J Natl Cancer Inst. 1996;88(8):542-549.
neighbourhood support and financial burden with unmet needs of 196. Gillison ML, Zhang Q, Jordan R, et al. Tobacco smoking and
head and neck cancer survivors. Oral Oncol. 2017;65:57-64. increased risk of death and progression for patients with p16-posi-
177. Ramsey SD, Bansal A, Fedorenko CR, et al. Financial insolvency as a tive and p16-negative oropharyngeal cancer. J Clin Oncol. 2012;30
risk factor for early mortality among patients with cancer. J Clin (17):2102-2111.
Oncol. 2016;34(9):980-986. 197. Berthiller J, Lee YC, Boffetta P, et al. Marijuana smoking and the risk
178. Lee DH, Roh JL, Baek S, et al. Second cancer incidence, risk factor, of head and neck cancer: pooled analysis in the INHANCE consor-
and specific mortality in head and neck squamous cell carcinoma. tium. Cancer Epidemiol Biomarkers Prev. 2009;18(5):1544-1551.
Otolaryngol Head Neck Surg. 2013;149(4):579-586. 198. Schuckit MA. Treatment of opioid-use disorders. N Engl J Med.
179. Atienza JA, Dasanu CA. Incidence of second primary malignancies 2016;375(4):357-368.
in patients with treated head and neck cancer: a comprehensive 199. Day AT, Tang L, Karam-Hage M, Fakhry C. Tobacco treatment pro-
review of literature. Curr Med Res Opin. 2012;28(12):1899-1909. grams at National Cancer Institute-designated cancer centers: a sys-
180. Dikshit RP, Boffetta P, Bouchardy C, et al. Risk factors for the devel- tematic review and online audit. Am J Clin Oncol. 2019;42(4):407-410.
opment of second primary tumors among men after laryngeal and 200. Nayan S, Gupta MK, Sommer DD. Evaluating smoking cessation
hypopharyngeal carcinoma. Cancer. 2005;103(11):2326-2333. interventions and cessation rates in cancer patients: a systematic
181. Baxi SS, Pinheiro LC, Patil SM, Pfister DG, Oeffinger KC, Elkin EB. review and meta-analysis. ISRN Oncol. 2011;2011:849023.
Causes of death in long-term survivors of head and neck cancer. 201. Shingler E, Robles LA, Perry R, et al. Systematic review evaluating
Cancer. 2014;120(10):1507-1513. randomized controlled trials of smoking and alcohol cessation inter-
182. Bernat L, Hrusak D. Hypothyroidism after radiotherapy of head and ventions in people with head and neck cancer and oral dysplasia.
neck cancer. J Craniomaxillofac Surg. 2014;42(4):356-361. Head Neck. 2018;40(8):1845-1853.
183. Diaz R, Jaboin JJ, Morales-Paliza M, et al. Hypothyroidism as a con- 202. Force USPST, Curry SJ, Krist AH, et al. Screening and behavioral
sequence of intensity-modulated radiotherapy with concurrent counseling interventions to reduce unhealthy alcohol use in adoles-
taxane-based chemotherapy for locally advanced head-and-neck cents and adults: US preventive services task Force recommenda-
cancer. Int J Radiat Oncol Biol Phys. 2010;77(2):468-476. tion statement. JAMA. 2018;320(18):1899-1909.
184. Garcia-Serra A, Amdur RJ, Morris CG, Mazzaferri E, Mendenhall 203. Moyer VA. Preventive services task F. screening and behavioral
WM. Thyroid function should be monitored following radiotherapy counseling interventions in primary care to reduce alcohol misuse:
to the low neck. Am J Clin Oncol. 2005;28(3):255-258. U.S. preventive services task force recommendation statement. Ann
185. Sroussi HY, Epstein JB, Bensadoun RJ, et al. Common oral complica- Intern Med. 2013;159(3):210-218.
tions of head and neck cancer radiation therapy: mucositis, infec- 204. Rogers LQ, Courneya KS, Robbins KT, et al. Physical activity and
tions, saliva change, fibrosis, sensory dysfunctions, dental caries, quality of life in head and neck cancer survivors. Support Care Can-
periodontal disease, and osteoradionecrosis. Cancer Med. 2017;6 cer. 2006;14(10):1012-1019.
(12):2918-2931. 205. Sammut L, Fraser LR, Ward MJ, Singh T, Patel NN. Participation in
186. Epstein JB, Barasch A. Oral and dental health in head and neck can- sport and physical activity in head and neck cancer survivors: associ-
cer patients. Cancer Treat Res. 2018;174:43-57. ations with quality of life. Clin Otolaryngol. 2016;41(3):241-248.
23788038, 2022, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/lio2.702 by Spanish Cochrane National Provision (Ministerio de Sanidad), Wiley Online Library on [03/01/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
92 GOYAL ET AL.
206. Capozzi LC, Boldt KR, Lau H, Shirt L, Bultz B, Culos-Reed SN. A 221. Blake KD, Ottenbacher AJ, Finney Rutten LJ, et al. Predictors of
clinic-supported group exercise program for head and neck cancer human papillomavirus awareness and knowledge in 2013: gaps and
survivors: managing cancer and treatment side effects to improve opportunities for targeted communication strategies. Am J Prev Med.
quality of life. Support Care Cancer. 2015;23(4):1001-1007. 2015;48(4):402-410.
207. Eades M, Murphy J, Carney S, et al. Effect of an interdisciplinary 222. Luryi AL, Yarbrough WG, Niccolai LM, et al. Public awareness of
rehabilitation program on quality of life in patients with head and head and neck cancers: a cross-sectional survey. JAMA Otolaryngol
neck cancer: review of clinical experience. Head Neck. 2013;35(3): Head Neck Surg. 2014;140(7):639-646.
343-349. 223. Williams MU, Carr MM, Goldenberg D. Public awareness of human
208. Lonbro S, Dalgas U, Primdahl H, et al. Lean body mass and muscle func- papillomavirus as a causative factor for oropharyngeal cancer.
tion in head and neck cancer patients and healthy individuals – results Otolaryngol Head Neck Surg. 2015;152(6):1029-1034.
from the DAHANCA 25 study. Acta Oncol. 2013;52(7):1543-1551. 224. Milbury K, Rosenthal DI, El-Naggar A, Badr H. An exploratory study
209. Zhao SG, Alexander NB, Djuric Z, et al. Maintaining physical activity of the informational and psychosocial needs of patients with human
during head and neck cancer treatment: results of a pilot controlled papillomavirus-associated oropharyngeal cancer. Oral Oncol. 2013;
trial. Head Neck. 2016;38(suppl 1):E1086-E1096. 49(11):1067-1071.
210. Samuel SR, Maiya GA, Babu AS, Vidyasagar MS. Effect of exercise 225. D'Souza G, Zhang Y, Merritt S, et al. Patient experience and anxiety
training on functional capacity & quality of life in head & neck can- during and after treatment for an HPV-related oropharyngeal can-
cer patients receiving chemoradiotherapy. Indian J Med Res. 2013; cer. Oral Oncol. 2016;60:90-95.
137(3):515-520. 226. Schorr M, Carlson LE, Lau HY, et al. Distress levels in patients with
211. Ibrahim EM, Al-Homaidh A. Physical activity and survival after oropharyngeal vs. non-oropharyngeal squamous cell carcinomas of
breast cancer diagnosis: meta-analysis of published studies. Med the head and neck over 1 year after diagnosis: a retrospective
Oncol. 2011;28(3):753-765. cohort study. Support Care Cancer. 2017;25(10):3225-3233.
212. Qiu S, Jiang C, Zhou L. Physical activity and mortality in patients 227. Fakhry C, D'Souza G. Discussing the diagnosis of HPV-OSCC: com-
with colorectal cancer: a meta-analysis of prospective cohort stud- mon questions and answers. Oral Oncol. 2013;49(9):863-871.
ies. Eur J Cancer Prev. 2020;29(1):15-26. 228. Reich M, Licitra L, Vermorken JB, et al. Best practice guidelines in
213. Schmid D, Leitzmann MF. Association between physical activity and the psychosocial management of HPV-related head and neck can-
mortality among breast cancer and colorectal cancer survivors: a sys- cer: recommendations from the European Head and Neck Cancer
tematic review and meta-analysis. Ann Oncol. 2014;25(7):1293-1311. Society's Make Sense Campaign. Ann Oncol. 2016;27(10):1848-
214. Hutcheson KA, Barrow MP, Warneke CL, et al. Cough strength and 1854.
expiratory force in aspirating and nonaspirating postradiation head 229. Shelal Z, Cho D, Urbauer DL, et al. Knowledge matters and
and neck cancer survivors. Laryngoscope. 2018;128(7):1615-1621. empowers: HPV vaccine advocacy among HPV-related cancer survi-
215. Laciuga H, Rosenbek JC, Davenport PW, Sapienza CM. Functional vors. Support Care Cancer. 2020;28(5):2407-2413.
outcomes associated with expiratory muscle strength training: nar- 230. Finnigan JP Jr, Sikora AG. Counseling the patient with potentially
rative review. J Rehabil Res Dev. 2014;51(4):535-546. HPV-related newly diagnosed head and neck cancer. Curr Oncol Rep.
216. Hutcheson KA, Barrow MP, Plowman EK, et al. Expiratory 2014;16(3):375.
muscle strength training for radiation-associated aspiration after 231. Khariwala SS, Moore MG, Malloy KM, Gosselin B, Smith RV. The
head and neck cancer: a case series. Laryngoscope. 2018;128(5): “HPV discussion”: effective use of data to deliver recommendations
1044-1051. to patients impacted by HPV. Otolaryngol Head Neck Surg. 2015;153
217. Palmer AD, Bolognone RK, Thomsen S, Britton D, Schindler J, (4):518-525.
Graville DJ. The safety and efficacy of expiratory muscle strength 232. D'Souza G, Robbins HA. Sexual and relationship health among survi-
training for rehabilitation after supracricoid partial laryngectomy: a vors of oropharyngeal or oral cavity squamous cell carcinoma. Can-
pilot investigation. Ann Otol Rhinol Laryngol. 2018;128:169-176. cer. 2017;123(7):1092-1094.
218. Mitchell RB, Hussey HM, Setzen G, et al. Clinical consensus state-
ment: tracheostomy care. Otolaryngol Head Neck Surg. 2013;148(1):
6-20.
219. Garg S, Kozin E, Deschler D. Care of the post-laryngectomy stoma How to cite this article: Goyal N, Day A, Epstein J, et al. Head
#281. J Palliat Med. 2014;17(7):857-858. and neck cancer survivorship consensus statement from the
220. Brook I, Bogaardt H, van As-Brooks C. Long-term use of heat and
American Head and Neck Society. Laryngoscope Investigative
moisture exchangers among laryngectomees: medical, social, and
psychological patterns. Ann Otol Rhinol Laryngol. 2013;122(6): Otolaryngology. 2022;7(1):70-92. doi:10.1002/lio2.702
358-363.