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Tonsil Cancer
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Tonsil Cancer
Authors
Affiliations
1 Imperial College London
2 Hillcrest Medical Center
3 SUNY Upstate Medical University
Objectives:
Employ interprofessional team strategies for improving care coordination and communication to advance the
management of tonsil cancer and improve patient outcomes.
Introduction
Tonsil cancer is the most common form of oropharyngeal malignancy, and its incidence is sharply rising due to the
increasing prevalence of human papillomavirus (HPV)-induced cancers. The presence of HPV can dramatically alter
the prognosis of tonsillar cancer, and there have recently been significant changes made to the WHO classification
and TNM staging to reflect this. Tonsil cancer can be managed by both surgical and oncological approaches, although
the optimal treatment regimen remains an area of ongoing research.
Etiology
Traditionally, oropharyngeal and tonsil cancers were attributed to smoking and alcohol misuse, with the former
remaining an independent indicator of poor prognosis. In more recent years; however, there has been a sharp increase
in the number of cases occurring secondary to HPV, with up to 93% of new oropharyngeal cancers in Western
Europe showing HPV positivity.[1] Additionally, there is a growing body of evidence to suggest having a spouse with
HPV-related cancer can result in a slight increase in the likelihood of developing oropharyngeal and anogenital
cancers.[2]
Epidemiology
Large epidemiological studies have shown tonsils are the most common site of oropharyngeal cancer, compromising
23.1% of all malignancies in this anatomical region, with an overall incidence rate of 8.4 cases per 100,000.[3] Of
concern, the rate of tonsil and oropharyngeal cancers has increased dramatically in the last 40
years. This significant rise has been attributed to the "viral epidemic" of HPV, with western countries seeing an
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increase in the proportion of HPV-associated cancers from 42.5% before 2000 to 72.2% between 2005 and
2009. Conversely, was not a significant increase in the rate of non-HPV oropharyngeal cancers within the same
period.[4]
Histopathology
HPV is a double-stranded DNA virus implicated in a host of carcinomas throughout the body. HPV 16 has the
greatest association with oropharyngeal cancers, with other oncogenic strains including HPV 18 being less
common[5]. p16 is a tumor-suppressor protein that is overexpressed in HPV-positive tumors and is well established as
a useful surrogate marker of HPV in tonsil cancer.[6]
The fourth edition of the World Health Organization's Classification of Head and Neck Tumors has made a number of
changes to reflect our current understanding of the disease. Oral and oropharyngeal cancers are now separate clinical
entities, due to the presence of lymphoepithelial tissues within areas such as the tonsils. Most tonsil cancers are
squamous cell carcinomas (SCC). However, the WHO classification now subdivides this into two distinct
morphological groups; HPV positive and HPV negative. HPV positive SCCs arise from the deep lymphoid tissue of
the tonsillar crypts and have a non-keratinising morphology. HPV negative SCC develops from the
oropharyngeal/tonsil surface epithelium and is associated with keratinizing dysplasia.[7]
HPV-positive tumors will typically present in younger non-smoking patients of either gender, while HPV-negative
tumors will present in older male smokers with more co-morbidities, and thus have a poorer prognosis overall.
Patients require a full ear, nose, and throat examination by an experienced otolaryngologist, including palpation of the
neck for cervical lymphadenopathy and close inspection of the oropharynx. Particular attention should be paid to the
tonsil beds as primary cancers can be missed within the tonsil crypts. Flexible nasal endoscopy should be performed
in all patients for a thorough assessment of the oropharynx including inspection of the tonsils, tongue base, vallecula,
and lateral pharyngeal wall for signs of local invasion.
Evaluation
Imaging
All cases of tonsillar cancer will need through pre-treatment cross-sectional imaging, with contrast-enhanced MRI
providing the best quality soft tissue delineation of the primary disease and local spread.[8] CT can also assess the
primary disease although an artifact from adjacent dental treatments often limits this. CT is currently the imaging
modality of choice for staging all head and neck cancers and should be performed from skull base to diaphragm to
look for associated nodal and pulmonary disease.[9]
PET-CT can also be used in tonsil cancer as a means to help with diagnosis and staging in difficult to detect
cancers[10] and in post-treatment surveillance.[11]. However, it is limited by its false-positive findings, frequently
showing uptake in contralateral tonsils,[12] tongue base and Waldeyer's ring[10] without the presence of malignancy.
Endoscopy
It is strongly recommended all suspected tonsillar cancers undergo an examination under anesthesia and
panendoscopy.[13] This can facilitate close assessment and biopsy of the disease, planning of surgical interventions,
and exclusion of secondary malignancies within the upper airway and esophagus. FNA biopsies have been used in
those who are unfit for surgery; however, the reliability of HPV testing in cytology samples has been questioned.[14]
Treatment / Management
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Surgical Management
Early tonsil cancer is preferably managed with single modality treatment, with transoral robotic surgery (TORS) and
transoral laser microsurgery (TLM) having comparable oncological outcomes.[15] TORs is growing in popularity and
has been shown to have reduced operating time, shorter hospital stay, and improved swallowing recovery compared to
open techniques[16]; although, persistent severe dysphagia can occur post-operatively.[17] TLM is less widely
adopted and involves removal of the tumor in several pieces, making a histological examination of margins difficult.
[13] Regardless of the method of surgical intervention, it is advised to remove both tonsils at time of surgery due to a
small rate of bilateral synchronous tonsillar cancers.[18]
In more advanced disease, TLM or TORS can still be offered for early T3 tumors; however, this is often not possible
for T4 malignancies. Most of these cases will instead undergo chemoradiotherapy, as a surgical intervention will
usually require a mandibulotomy and extensive surgical reconstruction resulting in poor post-operative functional
outcomes.[13]
Given the high rate of nodal disease in both early and advanced tonsillar cancer, it is recommended that most cases
undergoing surgical intervention should also have an elective level II to IV neck dissection.[19]
Oncological Management
Primary radiotherapy for early tonsillar cancer has been shown to have good oncological outcomes and overall
survival. Unilateral radiotherapy to levels II to IV can be used in non-lateralized cancers with a low rate of
contralateral nodal recurrence and improved rates of radiation toxicity.[20] It is advised to treat those with
contralateral nodes with bilateral radiotherapy.[13]
A previous Cochrane review has established chemoradiotherapy as the management of choice for advanced tonsil and
oropharyngeal cancers.[21] This avoids the need for extensive surgery which carries significant long-term morbidity
and often requires post-operative chemoradiotherapy. Radiotherapy in addition to concurrent platinum-based cisplatin
chemotherapy is the most widely used regime, with the monoclonal antibody cetuximab being used as an equally
effective alternative in cases where cisplatin is contraindicated (renal impairment and hearing loss).[22]
Differential Diagnosis
The histological differential diagnosis of suspected tonsillar cancer includes;
Lymphoma
Several case reports document rare primary sites metastasizing to the tonsil including Merkel cell
carcinoma[24], renal cell carcinoma,[25] rectal adenocarcinoma,[26] and small cell lung cancer[27]
Staging
Tonsil malignancy is staged as oropharyngeal cancer according to the AJCC TNM classification of malignant tumors.
The 2016 eight edition splits oropharyngeal cancer into p16 positive and negative cancers to reflect the
current understanding of the influence of HPV and p16 on the prognosis and management.[28] This marks a dramatic
change from previous editions of the manual, and can significantly alter the final staging of the malignancy.
T3: Tumor greater than 4 cm or extension into the lingual surface of epiglottis
T4a: Tumor invades larynx, deep/extrinsic muscle of tongue, medial pterygoid, hard palate, or mandible
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T4b: Tumor invades lateral pterygoid muscle, pterygoid plates, lateral nasopharynx, skull base; or
encases carotid artery
T4: Larynx, deep/extrinsic muscle of tongue, medial pterygoid, hard palate, mandible, lateral pterygoid
muscle, pterygoid plates, lateral nasopharynx, skull base; or encases carotid artery
N2
N2a: Single ipsilateral node greater than 3 cm but less than 6cm
N3
M Classification
Prognosis
Prognosis of tonsil cancer is dependent on the HPV status of the tumor, with HPV positive tumors showing a 5-
year overall survival of 71% compared to 46% in HPV negative disease in one study.[29] However, this survival
benefit can be negated by the presence of smoking, with mortality rates being significantly higher in HPV-positive
smokers compared to non-smokers.[30] Other factors including low volume tumors, lack of nodal disease, young age,
low comorbid status, and presence of tumor invading lymphocytes are thought to influence prognosis in
oropharyngeal tumors positively.[31] There are no studies directly comparing survival outcomes in tonsil cancers
managed with a single modality surgical or oncological management.
Complications
Untreated tonsillar cancer will result in gradual growth and invasion of local structures. Invasion of the lateral
pterygoid muscle, pterygoid plates, lateral nasopharynx, skull base and encasement around the carotid is suggestive of
unresectable T4b disease in p16 negative cancers. Moreover, invasion of the skull base and vertebral tissues can
interfere with emerging nerves, resulting in Horner's syndrome and palsies of the brachial plexus and phrenic nerve.
Encasement of the carotid artery can cause a life-threatening carotid blow-out.
The management options of tonsil cancer can also carry significant complications. TORS can result in significant pain
and dysphagia postoperatively, particularly in advanced disease. Radiotherapy frequently causes mucositis,
xerostomia, and skin reactions, which can also have a significant impact on swallowing.[32] These effects can be
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amplified in those who undergo TORS resection with post-operative chemo-radiotherapy, who have reported
significantly worse swallowing and quality of life outcomes compared to those undergoing single modality
treatments.[33]
Consultations
Otolaryngologists
Oncologists
Radiologists
Plastic/maxillofacial surgeons
Restorative dentists
Dieticians
Palliative care
References
1. Näsman A, Attner P, Hammarstedt L, Du J, Eriksson M, Giraud G, Ahrlund-Richter S, Marklund L, Romanitan
M, Lindquist D, Ramqvist T, Lindholm J, Sparén P, Ye W, Dahlstrand H, Munck-Wikland E, Dalianis T. Incidence
of human papillomavirus (HPV) positive tonsillar carcinoma in Stockholm, Sweden: an epidemic of viral-induced
carcinoma? Int J Cancer. 2009 Jul 15;125(2):362-6. [PubMed: 19330833]
2. Mirghani H, Sturgis EM, Aupérin A, Monsonego J, Blanchard P. Is there an increased risk of cancer among
spouses of patients with an HPV-related cancer: A systematic review. Oral Oncol. 2017 Apr;67:138-145.
[PubMed: 28351568]
3. Weatherspoon DJ, Chattopadhyay A, Boroumand S, Garcia I. Oral cavity and oropharyngeal cancer incidence
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24. Vasileiadis I, Sofopoulos M, Arnogiannaki N, Georgopoulos S. A Merkel-cell carcinoma metastatic to the tonsil:
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23911145]
25. Massaccesi M, Morganti AG, Serafini G, Di Lallo A, Deodato F, Picardi V, Scambia G. Late tonsil metastases
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