Published September 1996 | Version v1
Journal article

Total body irradiation for bone marrow transplantation

Description

Purpose/Objective: The primary goal of this course is to develop an understanding of the rationale for the use of total body irradiation (TBI) as a component of cytoreduction for bone marrow transplantation, the techniques used, and the results of changing important parameters, such as dose, dose rate, and fractionation. Materials and Methods: Basic radiobiological principles relevant to TBI are reviewed; in particular, emphasis is placed on cell and animal studies which suggest means of optimizing TBI delivery to achieve maximum tumor cell kill and immunosuppression along with minimal normal tissue damage. Techniques utilized at various centers are described, with some discussion of achieving homogeneity, as well as inhomogeneity when desired with partial shielding or 'boosting'. A review of clinical studies, both randomized and non-randomized, is done; these are then interpreted in terms of potential optimization of the TBI parameters. Finally, comparison of TBI-containing regimens with chemotherapy-only regimens is done. Results: Radiobiological studies suggest a potential advantage for fractionated TBI over single dose TBI. Clinical studies support this view: highly fractionated regimens have allowed higher total doses to be used to increase malignant cell kill and immunosuppression without increasing toxicity. Randomized studies of TBI combined with VP-16 or cyclophosphamide versus busulfan combined with cyclophosphamide have either shown an advantage with TBI (in acute myelocytic leukemia in first remission) or no difference (in chronic myelogenous leukemia, chronic phase). Conclusion: TBI has been an effective component of cytoreductive regimens for marrow transplantation in patients with malignant disease, especially leukemias, which constitute 73% of all marrow transplants worldwide. Evidence supports fractionated TBI, to doses ≥ 13 Gy, when compared with single dose TBI. Randomized studies support the continued use of TBI in AML, and suggest that busulfan may be able to replace TBI for CML, but long-term results are pending

Additional details

Identifiers

PII
S036030169785290X;

Publishing Information

Journal Title
International Journal of Radiation Oncology, Biology and Physics
Journal Volume
36
Journal Issue
1
Journal Page Range
p. 135
ISSN
0360-3016
CODEN
IOBPD3

Conference

Title
38. annual meeting of the American Society for Therapeutic Radiology and Oncology (ASTRO)
Dates
27-30 Oct 1996
Place
Los Angeles, CA (United States)

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
34060708
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Resource subtype / Literary indicator
Conference
Descriptors DEI
BONE MARROW; CHEMOTHERAPY; ENDOXAN; FRACTIONATED IRRADIATION; TRAINING; TRANSPLANTS; WHOLE-BODY IRRADIATION
Descriptors DEC
ALKYLATING AGENTS; ANIMAL TISSUES; BODY; DRUGS; EDUCATION; EXTERNAL IRRADIATION; HEMATOPOIETIC SYSTEM; IMMUNOSUPPRESSIVE DRUGS; IRRADIATION; MEDICINE; ORGANS; THERAPY

Optional Information

Copyright
Copyright (c) 1996 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.