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Guideline:

Practice guideline for the performance of total body irradiation

National Guideline Clearinghouse (NGC). Guideline summary: Practice guideline for the performance of total body irradiation In: National Guideline Clearinghouse (NGC) [Web site]. Rockville (MD): cited 2006. Available: http://www.guideline.gov.


Bibliographic Source(s)

  • American College of Radiology (ACR). ACR practice guideline for the performance of total body irradiation. Reston (VA): American College of Radiology (ACR); 2006. 5 p. [6 references]

Guideline Status

This is the current release of the guideline.

Guideline Category

Management
Treatment

Intended Users

Advanced Practice Nurses
Allied Health Personnel
Nurses
Physician Assistants
Physicians

Guideline Objective(s)

  • To assist practitioners in providing effective and safe radiologic care for patients
  • To describe principles of practice for total body irradiation in hematologic malignancies

Target Population

Patients undergoing total body irradiation (TBI) for cytoreduction and immunosuppression

Interventions and Practices Considered

  1. Total body irradiation (TBI) including
    • Clinical evaluation
    • Obtaining informed consent
    • Treatment planning
    • Simulation of treatment
    • Dose calculations
    • Treatment delivery and treatment aids
  2. Qualifications and responsibilities of personnel
  3. Patient and personnel safety measures
  4. Types of equipment needed
  5. Documentation
  6. Continuing medical education programs for medical staff
  7. Quality control and improvement and patient education

Major Outcomes Considered

Not stated

Methods Used to Collect/Select Evidence

Searches of Electronic Databases

Description of Methods used to Collect/Select the Evidence

Not stated

Number of Source Documents

Not stated

Methods Used to Assess the Quality and Strength of the Evidence

Not stated

Rating Scheme for the Strength of the Evidence

Not applicable

Methods Used to Analyze the Evidence

Review

Description of the Methods Used to Analyze the Evidence

Not stated

Methods Used to Formulate the Recommendations

Expert Consensus

Description of Methods Used to Formulate the Recommendations

This guideline was revised collaboratively with the American College of Radiology (ACR) and the American Society for Therapeutic Radiology and Oncology (ASTRO).

Each practice guideline and technical standard representing a policy statement by the American College of Radiology (ACR) has undergone a thorough consensus process in which it has been subjected to extensive review requiring the approval of the Commission on Quality and Safety as well as the ACR Board of Chancellors the ACR Council Steering Committee and the ACR Council.

Rating Scheme for the Strength of the Recommendations

Not applicable

Cost Analysis

A formal cost analysis was not performed and published cost analyses were not reviewed.

Method of Guideline Validation

External Peer Review
Internal Peer Review

Description of Method of Guideline Validation

The guidelines are approved by the Commission on Quality and Safety as well as the American College of Radiology (ACR) Board of Chancellors the ACR Council Steering Committee and the ACR Council.

Major Recommendations

Fractionated total body irradiation (TBI) in conjunction with the use of chemotherapeutic agents has proven useful for cytoreduction and immunosuppression prior to bone marrow or peripheral blood stem cell transplantation for hematologic and other malignancies and for various genetic disorders. Unique features of TBI rendering it a valuable component of transplant preparative regimens in contrast to chemotherapy include:

  1. No sparing of "sanctuary" sites (e.g. testes)
  2. Dose homogeneity regardless of blood supply
  3. No known cross-resistance with other agents
  4. No problems with excretion or detoxification
  5. Ability to tailor the dose distribution by shielding specific organs or by "boosting" sites

Single fraction low dose TBI has recently emerged as an effective form of immunosuppression (with or without chemotherapy) prior to allogeneic stem cell transplantation in nonmyeloablative approaches.

The purposes of TBI are primarily to immunosuppress (in allogeneic transplants) and to cytoreduce (eradicate malignant cells or occasionally cell populations with genetic disorders).

It is essential that the complicated treatment and care of the patient receiving a transplant regimen containing TBI is well coordinated among the various services (medical oncology radiation oncology etc.) and caregivers (physicians nurses physicists psychologists dieticians etc). Unlike most other treatment delivered by a radiation oncologist fractionated TBI delivers results in myeloablation that is potentially lethal without intensive medical support and stem cell backup. Incorrectly delivered TBI may result in fatal toxicity as well. Thus great care must be taken by the entire TBI team to assure the best possible multidisciplinary treatment plan with attention to all facets of TBI.

Although the techniques vary widely from institution to institution certain basic principles apply such as the achievement of dose homogeneity throughout the body with the exception of shielded or boosted areas. The planning and performance of TBI is a team effort that requires close interaction and coordination among the radiation oncologist the medical physicist dosimetrists nurses and radiation therapists.

This guideline describes a quality assurance program for TBI and is supplementary to the ACR Practice Guideline for Radiation Oncology (see National Guideline Clearinghouse summary) and the ACR Technical Standard for the Performance of Radiation Oncology Physics for External Beam Therapy.

Process of Total Body Irradiation

The use of TBI is a complex process involving many trained personnel who carry out highly coordinated activities.

  1. Clinical Evaluation

    The initial evaluation should include a detailed history including a review of issues that may impact upon treatment tolerance (previous radiotherapy to sensitive organs factors affecting pulmonary renal or hepatic function and exposure to infectious agents); physical examination; review of all pertinent diagnostic and laboratory tests; and communication with the referring physician and other physicians involved in the patient's care in accordance with the ACR Practice Guideline for Communication: Radiation Oncology. Careful review of the applicable protocol for the particular disease being treated is essential since standardized institutional or cooperative group protocols are the norm for transplantation.

    As with delivery of any chemotherapy or radiotherapy policies and procedures should be in place to determine whether a female patient is pregnant before initiating any component of a transplant program including TBI. If the patient is determined to be pregnant alternative therapies in an effort to preserve the pregnancy versus termination of pregnancy and continuation with transplantation must be decided upon.

  1. Informed Consent

    Prior to simulation and treatment informed consent must be obtained and documented and must be in compliance with applicable laws regulations or policies. This should include a detailed discussion of the benefits and potential tissue-specific acute and late toxicities of TBI as well as the details of rationale for and alternatives to TBI.

  1. Treatment Planning

    Treatment planning for TBI requires detailed knowledge of the specific transplant program to be followed (either on or off of a clinical trial). Specific treatment parameters to be determined in advance of treatment include: field size dose per fraction dose rate total dose fractions per day interval between fractions if relevant beam energy geometry to achieve dose homogeneity bolus or beam spoilers to increase skin dose shielding and dose compensation requirements (e.g. lungs kidneys) and boost specifications (e.g. testes). Patient thickness measurements should be obtained at the prescription point (often at the level of the umbilicus) and at other points of interest for possible dose calculations and homogeneity determinations such as head neck mid-mediastinum mid-lung pelvis knee ankle etc. Patient height is recorded in order to determine the appropriate source-to-patient distance to appropriately fit the patient within the beam with sufficient margin around the patient (>5 cm usually).

  1. Simulation of Treatment

    For lung or other organ blocking simulation or other treatment planning is generally done in the treatment position (i.e. if the patient is standing for TBI the simulation should be done in the standing position if possible). If the planning session is performed in another position positional differences in organ location should be taken into account and the medical physicist should be consulted. Reference points for block placement at the time of treatment should be marked on the patient's body for reproducibility.

  1. Calculations

    Calculations are performed by the medical physicist or his or her designee to determine beam-on time to achieve the prescribed dose dose homogeneity in the locations specified by the protocol and doses at any other points of concern. A medical physicist or a dosimetrist who did not perform the initial computation shall independently check the calculation before the first fraction is delivered. In vivo dosimetry may aid in assessment of dose homogeneity. Every effort should be made to maintain dose inhomogeneity to within +/-10%.

  1. Treatment Aids

    Special TBI stands or tables are often used to aid in immobilization placement of organ shields and patient support and comfort.

  1. Treatment Delivery

    TBI containing myeloablative transplant programs typically utilize fractionated or hyperfractionated regimens (twice a day or three times a day) over several days in order to minimize both acute and chronic toxicities and to minimize overall treatment time. Prior to treatment any shielding of normal organs should be checked with portal images. In the setting of single fraction low-dose TBI where total doses are typically only 200 cGy organ shielding is not utilized. Dosimetry should be checked against department protocols to verify dose delivery at the extended distances that are usually used for treatment. A medical physicist should be available during all treatments in case of questions regarding dosimetric details equipment function patient setup etc. Treatments are carried out by the radiation therapist per the ACR Practice Guideline for Radiation Oncology.

    A physician should be in close proximity to manage any problems related to treatment. Avoidance of medications that may cause orthostatic hypotension (such as phenothiazines) and the administration of intravenous (IV) fluids for hydration or transfusions for anemia may help to prevent syncope or near-syncopal episodes when the patient is treated in the standing position.

Qualifications and Responsibilities of Personnel

Application of this guideline should be in accordance with the ACR Practice Guideline for Radiation Oncology.

  1. Radiation Oncologist

    The radiation oncologist shall have had training in TBI procedures prior to embarking on any of these regimens.

    The responsibilities of the radiation oncologist include:

    1. Consultation and decision-making regarding the course of treatment.
    2. Coordination of the patient's care with the transplantation service.
    3. Participation in the treatment planning process (immobilization techniques simulation block design prescription etc.).
    4. Review and verification of portal images.
    5. Clinical assessment of the patient's tolerance during the treatment course.
  1. Qualified Medical Physicist

    The responsibilities of the Qualified Medical Physicist include:

    1. Establishment and management of a quality assurance program for TBI performance.
    2. Acting as a technical resource for planning of immobilization devices dosimetry techniques shielding dose compensation devices and bolusing methods.
    3. Calibration of the external beam delivery system.
    4. Direct supervision of dosimetry measurements and calculations for TBI delivery.
  1. Dosimetrist

    The responsibilities of the dosimetrist include:

    1. Generation of the dose calculations for treatment.
    2. Dosimetry measurements.
  1. Radiation Therapist

    The responsibilities of the radiation therapist include:

    1. Setting up the patient in the treatment position including using appropriate treatment devices.
    2. Performance of imaging procedures to verify the setup and blocking if any.
    3. Treatment of the patient according to the prescription and plan provided.
    4. Continuing monitoring and evaluation of the patient during the treatments.
    5. Verification that the prescribed and calculated treatment distances match the utilized treatment distances.
  1. Nurse

    The responsibilities of the nurse may include:

    1. Monitoring the patient's tolerance of the procedure to promote adequate supportive care.
    2. Communicating any special precautions to the rest of the team regarding the care of immunosuppressed patients.

Equipment

High-energy photon beams are used for TBI generally delivered by linear accelerators in the range of 4–18 MV or by a Co-60 unit. Additional equipment may include a fluoroscopy or computed tomography (CT) simulator immobilization devices equipment for the manufacture of shielding computers for dose calculations a beam spoiler custom bolus custom compensators and dosimetry and calibration devices. A backup beam delivery system must be available in case of unanticipated machine failure.

Patient and Personnel Safety

  1. Safety measures should be in accordance with the ACR Practice Guideline for Radiation Oncology.
  2. Special Patient Protection Measures
    1. Charting systems for prescription; delineation of treatment parameters of the setup; including any position settings of the TBI stand; and treatment delivery record including time of delivery for multiple treatments in a day.
    2. Physics program for calibration of the treatment machine independent checking of dose calculations and monitoring of dose delivery to the patient.
    3. Visual and audio contact with the patient during treatment.

Documentation

Reporting should be in accordance with the ACR Practice Guideline for Communication: Radiation Oncology.

Educational Program

Continuing medical education programs should include radiation oncologists physicists dosimetrists nurses and radiation therapists. The program should be in accordance with the ACR Practice Guideline for Continuing Medical Education (CME).

Quality Control and Improvement Safety Infection Control and Patient Education Concerns

See the "Description of the Implementation Strategy" field below.

Clinical Algorithm(s)

None provided

Type of Evidence supporting the Recommendations

The type of supporting evidence is not specifically stated for each recommendation.

Potential Benefits

Appropriate performance of total body irradiation to ensure accurate and safe treatment

Potential Harms

  • Potential toxicities of total body irradiation (TBI)
  • Unlike most other treatment delivered by a radiation oncologist fractionated TBI delivers results in myeloablation that is potentially lethal without intensive medical support and stem cell backup. Incorrectly delivered TBI may result in fatal toxicity as well.

Qualifying Statements

  • These guidelines are an educational tool designed to assist practitioners in providing appropriate radiologic care for patients. They are not inflexible rules or requirements of practice and are not intended nor should they be used to establish a legal standard of care. For these reasons and those set forth below the American College of Radiology cautions against the use of these guidelines in litigation in which the clinical decisions of a practitioner are called into question.
  • The ultimate judgment regarding the propriety of any specific procedure or course of action must be made by the physician or medical physicist in light of all the circumstances presented. Thus an approach that differs from the guidelines standing alone does not necessarily imply that the approach was below the standard of care. To the contrary a conscientious practitioner may responsibly adopt a course of action different from that set forth in the guidelines when in the reasonable judgment of the practitioner such course of action is indicated by the condition of the patient limitations on available resources or advances in knowledge or technology subsequent to publication of the guidelines. However a practitioner who employs an approach substantially different from these guidelines is advised to document in the patient record information sufficient to explain the approach taken.
  • The practice of medicine involves not only the science but also the art of dealing with the prevention diagnosis alleviation and treatment of disease. The variety and complexity of human conditions make it impossible to always reach the most appropriate diagnosis or to predict with certainty a particular response to treatment. Therefore it should be recognized that adherence to these guidelines will not assure an accurate diagnosis or a successful outcome. All that should be expected is that the practitioner will follow a reasonable course of action based on current knowledge available resources and the needs of the patient to deliver effective and safe medical care. The sole purpose of these guidelines is to assist practitioners in achieving this objective.

Description of Implementation Strategy

Quality Control and Improvement Safety Infection Control and Patient Education Concerns

Policies and procedures related to quality patient education infection control and safety should be developed and implemented in accordance with the ACR Policy on Quality Control Improvement Safety Infection Control and Patient Education Concerns appearing elsewhere in the ACR Practice Guidelines and Technical Standards book.

The Medical Director of Radiation Oncology is responsible for the institution and ongoing supervision of continuing quality improvement (CQI) as described in the ACR Practice Guideline for Radiation Oncology. It is the responsibility of the director to identify problems see that actions are taken and evaluate the effectiveness of the actions.

IOM Care Need

Getting Better
Living with Illness

IOM Domain

Effectiveness
Patient-centeredness
Safety

Bibliographic Source(s)

  • American College of Radiology (ACR). ACR practice guideline for the performance of total body irradiation. Reston (VA): American College of Radiology (ACR); 2006. 5 p. [6 references]

Adaptation

Not applicable: The guideline was not adapted from another source.

Source(s) of Funding

American College of Radiology

Guideline Committee

Collaborative Subcommittee
Guidelines and Standards Committee

Composition of Group that Authored the Guideline

Collaborative Subcommittee

American College of Radiology Committee Members: Rachel Rabinovitch MD Chair; Janice Kong-Ja Ryu MD; Jeffrey Y. C. Wong MD

American Society for Therapeutic Radiology and Oncology (ASTRO): Huan B. Giap MD PhD; Kenneth J. Russell MD; Paula J. Schomberg MD

Guidelines and Standards Committee

Committee Members: Laurie E. Gaspar MD MBA Chair; E. Brian Butler MD; Cassandra S. Foens MD; John S. Kent MS; Peter M. Mauch MD; LaMar S. McGinnis III MD; Rachel Rabinovitch MD; Seth A. Rosenthal MD; Anthony H. Russell MD; Oscar E. Streeter Jr. MD; Vipul V. Thakkar MD; Frank A. Vicini MD; Gregory M. Videtic MD CM; Steven A. Leibel MD Commission Chair

Financial Disclosures/Conflicts of Interest

Not stated

Guideline Status

This is the current release of the guideline.

Guideline Availability

Electronic copies: Available in Portable Document Format (PDF) from the American College of Radiology (ACR) Web site.

Print copies: Available from the American College of Radiology 1891 Preston White Drive Reston VA 20191. Telephone: (703) 648-8900.

Availability of Companion Documents

The following are available:

  • ACR practice guidelines and technical standards purpose and intended use. Reston (VA): American College of Radiology; 1 p. Electronic copies: Available in Portable Document Format (PDF) from the American College of Radiology (ACR) Web site.
  • The process for developing ACR practice guidelines and technical standards. Reston (VA): American College of Radiology; 1 p. Electronic copies: Available in Portable Document Format (PDF) from the American College of Radiology (ACR) Web site.

Patient Resources

None available

NGC STATUS

This NGC summary was completed by ECRI Institute on August 20 2007. The information was verified by the guideline developer on August 23 2007.

COPYRIGHT STATEMENT

Instructions for downloading use and reproduction of the American College of Radiology (ACR) Practice Guidelines & Technical Standards may be found on the ACR Web site.

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