2013 ASTRO e ACR - Practice Guideline For The Performance TBI
2013 ASTRO e ACR - Practice Guideline For The Performance TBI
2013 ASTRO e ACR - Practice Guideline For The Performance TBI
American Journal of Clinical Oncology Volume 36, Number 1, February 2013 www.amjclinicaloncology.com | 97
Wolden et al American Journal of Clinical Oncology Volume 36, Number 1, February 2013
Allogeneic grafts can be from related or unrelated individuals, challenges that must be considered/addressed to improve dose
but “matching” of donor and recipient is performed. The graft uniformity. Very young children who require anesthesia may
may be in the form of bone marrow, peripheral stem cells, and be treated lying on the floor with the gantry pointing downward
umbilical cord blood.2 and with the spoiler and blocks placed above the patient.
Unique features of TBI that make it a valuable component Successful planning and delivery of TBI requires close inter-
of transplant preparative regimens include: action and coordination among the radiation oncologist, med-
1. No sparing of “sanctuary” sites such as testes and the ical physicist, dosimetrists, nurses, and radiation therapists.
central nervous system. This guideline describes a quality assurance program for
2. Dose homogeneity to the whole body regardless of blood TBI and is supplementary to the ACR Practice Guideline for
supply. Radiation Oncology23 and the ACR Technical Standard for the
3. Less chance of cross-resistance with other antineoplastic Performance of Radiation Oncology Physics for External
agents (chemotherapy). Beam Therapy.24
4. No problems with excretion or detoxification.
5. Ability to tailor the dose distribution by shielding specific PROCESS OF TBI
organs or by “boosting” sites. The use of TBI is a complex process involving many
A wide variety of TBI dose and fractionation schedules trained personnel who carry out highly coordinated activities.
have been studied. The optimal regimen depends on a range of
clinical variables, including patient age, disease, and type of Clinical Evaluation
HSCT. With competing goals of disease eradication and The initial evaluation should include a detailed history,
avoidance of toxicity, the most commonly accepted total dose including a review of issues that may impact on treatment toler-
of TBI for myeloablative HSCT is 12 to 15 Gy delivered in 8 to ance (previous radiotherapy to sensitive organs, factors affecting
12 fractions over 4 days.3,4 Numerous investigators have pulmonary, renal, or hepatic function, and exposure to infectious
shown that efficacy is improved and a variety of important late agents); physical examination; review of all pertinent diagnostic
toxicities are significantly decreased when TBI is fractionated and laboratory tests; and communication with the referring
in 2 to 3 treatments per day.5,6 Relatively low-dose rates are physician and other physicians involved in the patient’s care in
also important for optimal outcome.7 Many protocols require a accordance with the ACR Practice Guideline for Communication:
dose rate of < 0.2 Gy per minute. Radiation Oncology.25 Careful review of the applicable treatment
Low-dose TBI, often in conjunction with chemotherapy, plan or clinical trial protocol for the particular disease being
has recently emerged as an effective form of conditioning in treated is essential as standardized institutional or cooperative
reduced intensity HSCT for patients who may not be able to group protocols are typically used for transplantation.
tolerate myeloablation because of poor performance status or As with delivery of any chemotherapy or radiotherapy,
comorbidity. Notable studies have included TBI doses of 2 to policies and procedures should be in place to determine
8 Gy in 1 to 4 fractions.8–12 whether a female patient is pregnant before initiating any
It is essential that the complicated treatment and care of component of a transplant program, including TBI. If the
the patient receiving TBI be well coordinated among the var- patient is determined to be pregnant, other therapies should be
ious subspecialties (medical oncology, radiation oncology, considered in an effort to preserve the pregnancy. Alter-
etc.) and caregivers (physicians, nurses, physicists, psycholo- natively, if the patient wishes to proceed with transplant, the
gists, dieticians, etc). TBI presents a unique challenge because pregnancy may be electively terminated.
it results in potentially lethal myeloablation without intensive
medical support and stem cell backup. Incorrectly delivered Informed Consent
TBI may result in fatal toxicity. Anticipated immediate tox- Before simulation and treatment, informed consent must be
icity includes the following signs and symptoms: nausea, obtained and documented and must be in compliance with
emesis, parotitis, xerostomia, headache, fatigue, mucositis, applicable laws, regulations, or policies, in accordance with the
diarrhea, and loss of appetite.13 Prophylactic interventions to ACR Practice Guideline on Informed Consent: Radiation Oncol-
manage these toxicities include intravenous hydration, antie- ogy.26 This should include a detailed discussion of the benefits and
metics, and antimucositis agents.14 Patients must be counseled potential tissue-specific acute and late toxicities of TBI, as well as
regarding the risks of long-term sequelae of TBI, which vary in the details of, rationale for, and alternatives to TBI.
incidence depending on the clinical scenario and TBI regimen.
These late risks may include pneumonopathy,15 veno-occlu- Treatment Planning
sive disease of the liver,16 kidney dysfunction,17 cataracts,7 Treatment planning for TBI requires detailed knowledge
hypothyroidism,18 infertility,19 and secondary malignancies.20 of the specific transplant program to be followed (either on or
Because of the significant risk associated with this treatment, off of a clinical trial). Specific treatment parameters to be
the entire team must take great care to assure the best possible determined in advance of treatment include: field size, colli-
multidisciplinary care with attention to all facets of TBI. mator rotation, treatment distance, dose per fraction, dose rate,
Although the techniques of TBI vary widely from insti- total dose, number of fractions per day, interval between
tution to institution, certain basic principles apply, such as the fractions, beam energy, geometry to achieve dose homoge-
achievement of relative-dose homogeneity throughout the neity, bolus or beam spoilers to increase skin dose, shielding
body, with the exception of intentionally shielded or boosted and dose compensation requirements (eg, lungs, kidneys), and
areas. Most centers use opposing anterior and posterior fields boost specifications (eg, testes, chest wall). Patient thickness
with the patient standing upright several meters from the measurements should be obtained at the prescription point
source and the beam pointed horizontally. A beam spoiler (often at the level of the umbilicus) and at other points of
placed upstream may be used to prevent skin sparing.21 interest for possible dose calculations and homogeneity
Alternatively, patients can be irradiated with lateral fields in a determinations, such as head, neck, mid-mediastinum, mid-
sitting or partly reclining position.22 This approach is usually lung, pelvis, knee, ankle, etc. Patient height is recorded to
better tolerated by patients but presents additional dosimetric determine the appropriate source-to-patient distance to fit
the patient within the beam with sufficient margin around the QUALIFICATIONS AND RESPONSIBILITIES OF
patient (usually >5 cm). Special attention should be paid to the PERSONNEL
dramatic decrease in dose that can be seen in the field corners Application of this guideline should be in accordance
for many treatment units when the collimator is in the full open with the ACR Practice Guideline for Radiation Oncology.23
position.
Radiation Oncologist
Simulation of Treatment The radiation oncologist should have had training in TBI
For lung or other organ blocking, simulation or other procedures before embarking on any of these regimens.
treatment planning is generally done in the treatment position, The responsibilities of the radiation oncologist include:
that is, if the patient is standing for TBI, the simulation should 1. Consultation and decision-making regarding the course of
be done in the standing position if possible. As an alternative to treatment.
computed tomography simulation in the supine position, lung 2. Coordination of the patient’s care with the transplantation
blocks may be designed on megavoltage radiographs generated service and other physicians.
by a linear accelerator with the patient in an upright position. If 3. Participation in the treatment planning process (immobili-
the planning session is performed in another position, posi- zation techniques, simulation, block design, prescription,
tional differences in organ location should be considered and dosimetric and physics review, etc).
the medical physicist should be consulted. Reference points for 4. Review of treatment verification images.
block placement at the time of treatment should be marked on 5. Clinical assessment of the patient’s tolerance during the
the patient’s body for reproducibility. treatment course.