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Home » Cancer Management Handbook, 11th Edition » Chapter 2: Principles of Radiation Therapy

Cancer Management: A Multidisciplinary Approach, 11th Edition (2008).
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Chapter 2 

Principles of Radiation Therapy

By Kevin A. Camphausen, MD, and Lawrence R. Coia, MD | April 9, 2009

TREATMENT PLANNING AND DELIVERY

Determining optimal dose distribution The medical physicist or do­simetrist uses the information from CT and simulation to plan the treatment on a computer. A complete collection of machine data, including depth dose and beam profile information, is stored in the computer. The physics staff aids the radiation oncologist in deciding the number of beams (usually two to four) and angles of entry. The goal is to maximize the dose to the tumor while minimizing the dose to surrounding normal structures.

Several treatment plans are generated, and the radiation oncologist chooses the optimal dose distribution. The beam-modifying devices discussed earlier, such as blocks and wedges, may be used to optimize the dose distribution around the tumor.

Establishing the treatment plan The planning computer will calculate the amount of time each beam should be on during treatment. All pertinent data, such as beam-on time, beam angles, blocks, and wedges, are recorded in the patient’s treatment chart and sent to the treatment machine. The radia­tion therapist will use this information, as well as any casts, tattoos, and lasers, to set up and treat the patient consistently and accurately each day.

Taking weekly port films As part of departmental quality assurance, weekly port films are taken for each beam. They ensure that the beams and blocks are consistently and correctly placed for each treatment. Port films are images generated by the linear accelerator at energies of 6—20 MeV. Because of the pre­dominance of the Compton effect in this energy range, these images are not as detailed as those at diagnostic film energies (as mentioned earlier), but they still provide important information on treatment accuracy and ensure the quality of setup and treatment.

BRACHYTHERAPY

Brachytherapy is the term used to describe radiation treatment in which the radiation source is in contact with the tumor. This therapy contrasts with external-beam radiotherapy, in which the radiation source is 80—100 cm away from the patient.

In brachytherapy, dose distribution is almost totally dependent on the inverse square law because the source is usually within the tumor volume. Because of this inverse square dependence, the proper placement of radiation sources is crucial.

Isotopes Table 2 lists commonly used isotopes and their properties. In the past, radium was the primary isotope used in brachytherapy. Recently, because of its long half-life and high energy output, Click to Enlargeradium has been replaced with cesium (Cs), gold (Au), and iridium (Ir). These isotopes have shorter half-lives than radium and can be shielded more easily because of their lower energies.

Types of implants Brachytherapy procedures can be performed with either temporary or permanent implants. Temporary implants usually have long half-lives and higher energies than permanent implants. These sources can be manufactured in several forms, such as needles, seeds, and ribbons.

All temporary sources are inserted into catheters that are placed in the tumor during surgery. A few days after surgery, the patient is brought to the radiation clinic and undergoes pretreatment simulation. Wires with nonradioactive metal seeds are threaded into these catheters. Several films are taken, and the images of the seed placement can be digitized into a brachytherapy treatment planning computer.

Once the treatment plan is complete and the physician has chosen the optimal dose rate (usually 50—60 cGy/h), the sources can be implanted. The actual implantation takes place in the patient’s private room. The duration of treatment is usually 1 to 3 days. The majority of temporary implants are loaded interstitially.

Common uses Interstitial low-dose–rate (LDR) brachytherapy is com­monly used for cancer of the oral cavity and oropharynx and sarcoma. Prostate cancer is probably the most common site for which LDR brachytherapy “seeds” are used today. Intracavitary LDR brachytherapy is frequently used in gynecologic applica­tions. High-dose–rate (HDR) brachytherapy is used with remote afterloading techniques, as described below.

Remote afterloading brachytherapy

Because brachytherapy requires numerous safety precautions and entails unnecessary exposure of personnel and family members to radiation, remote after­loading of temporary implants has become popular in recent years. The two types of remote afterloading that can be used for treatment are LDR and HDR sources. The most popular LDR source used today is Cs-137, which has a dose rate of about 1 cGy/min. The most widely used HDR source is Ir-192. This isotope has a dose rate of about 100 cGy/min.

General procedures The pretreatment brachytherapy procedures out­lined above are also implemented in remote afterloading brachytherapy. Once the treatment plan has been approved by the physician, the patient is brought into the treatment room. The LDR cesium source or HDR iridium source is connected to the end of a cable inside its respective afterloading unit. This unit is programmed with the data from the planning computer. The cable is sent out from the unit into one of the patient’s catheters. Several catheters can be connected to the unit. Each catheter is irradiated, one at a time, until the prescribed dose has been delivered.

The motor that drives the source out of the treatment unit is connected elec­tronically to the door of the treatment room. If the treatment must be stopped for any reason, simply opening the door triggers an interlock that draws the source back into the unit. Because of this device, oncology person­nel will not be exposed to any radiation should they need to see the patient during treatment. This interlock is the main safety advantage of remote af­terloading over manual afterloading.

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Table of Contents

Chapter 1: Head and Neck Tumors

Chapter 2: Thyroid and Parathyroid Cancers

Chapter 3: Non-Small-Cell Lung Cancer

Chapter 4: Small-Cell Lung Cancer, Mesothelioma, and Thymoma

Chapter 5: Breast Cancer Overview

Chapter 6: Stages 0 and I breast cancer

Chapter 7: Stage II breast cancer

Chapter 8: Stages III and IV breast cancer

Chapter 9: Esophageal cancer

Chapter 10: Gastric cancer

Chapter 11: Pancreatic, neuroendocrine GI, and adrenal cancers

Chapter 12: Liver, gallbladder, and biliary tract cancers

Chapter 13: Colon, rectal, and anal cancers

Chapter 14: Prostate cancer

Chapter 15: Testicular cancer

Chapter 16: Urothelial and kidney cancers

Chapter 17: Cervical cancer

Chapter 18: Uterine corpus tumors

Chapter 19: Ovarian cancer

Chapter 20: Melanoma and other skin cancers

Chapter 21: Bone sarcomas

Chapter 22: Soft-tissue sarcomas

Chapter 23: Primary and metastatic brain tumors

Chapter 24: AIDS-related malignancies

Chapter 25: Carcinoma of an unknown primary site

Chapter 26: Hodgkin lymphoma

Chapter 27: Non-Hodgkin lymphoma

Chapter 28: Multiple myeloma and other plasma cell dyscrasias

Chapter 29: Acute leukemias

Chapter 30: Chronic myeloid leukemia

Chapter 31: Chronic lymphocytic leukemia

Chapter 32: Myelodysplastic syndromes

Chapter 33: Hematopoietic cell transplantation

Chapter 34: Pain management

Chapter 35: Management of nausea and vomiting

Chapter 36: Depression, anxiety, and delirium

Chapter 37: Fatigue and dyspnea

Chapter 38: Anorexia and cachexia

Chapter 39: Oncologic emergencies and paraneoplastic syndromes

Chapter 40: Infectious complications

Chapter 41: Fluid complications

Color atlas The ABCDEs of moles and melanomas

Color atlas 2: Skin lesions

Color atlas 3: Dermatologic toxicities associated with targeted therapies

Appendix 1: Response Evaluation Criteria and Performance Scales

Appendix 2: Cancer Information on the Internet

Appendix 3: Cancer Drugs and Indications Newly Approved by the US Food and Drug Administration

Appendix 4: Chemotherapeutic Agents Their Uses, Dosages, and Toxicites

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