The general objectives of this research are to esblish quantitative criteria for evaluating the potential effectiveness of altered fractionation schemes in radiotherapy by developing models of tissue responses to fractionated doses and the development of more effective experimental designs and methods of analysis. More specifically, these studies are aimed at determining the influence of particular fractionation regimens on the rate of recovery during interfraction intervals and on the severity of the accompanying acute responses. Emphasis is placed on the application of applied mathematics to problems in experimental design and analysis, in which the emphasis is on determining the differential responses of normal tissues and tumors to various fractionation regimens. In particular, techniques are sought for obtaining quantitative, dose-response and repair kinetics parameters from qualitative assays of early and late normal tissue responses, as well as estimates of the response of human tumors to small fractional doses in order to predict radioresponsiveness. finally, the techniques of design and analysis will be made availabel to the experimental community through the development of exportable computer code. These studies might ultimately provide guidelines for the use of accelerated fractionation and hyperfractionation in radiotherapy, by determining the sites where it might be most beneficial and by establishing of the limits imposed on the number of daily treatments, both by the necessity for complete Elkind repair and by the level of acute response accompany these fractionation regimens.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA029026-09
Application #
3168474
Study Section
Radiation Study Section (RAD)
Project Start
1980-12-01
Project End
1989-11-30
Budget Start
1988-12-01
Budget End
1989-11-30
Support Year
9
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Texas MD Anderson Cancer Center
Department
Type
Hospitals
DUNS #
001910777
City
Houston
State
TX
Country
United States
Zip Code
77030
Thames, Howard D; Zhang, Ming; Tucker, Susan L et al. (2004) Cluster models of dose-volume effects. Int J Radiat Oncol Biol Phys 59:1491-504
Thames, Howard D; Petersen, Cordula; Petersen, Sven et al. (2002) Immunohistochemically detected p53 mutations in epithelial tumors and results of treatment with chemotherapy and radiotherapy. A treatment-specific overview of the clinical data. Strahlenther Onkol 178:411-21
Evans, S C; Mack, D C; Mason, K A et al. (2001) The proliferative response of mouse jejunal crypt cells to radiation-induced cell depletion is not mediated exclusively by transforming growth factor alpha. Radiat Res 155:866-9
Koscielny, S; Thames, H D (2001) Biased methods for estimating local and distant failure rates in breast carcinoma and a ""commonsense"" approach. Cancer 92:2220-7
Thames, H D; Ang, K K (1998) Altered fractionation: radiobiological principles, clinical results, and potential for dose escalation. Cancer Treat Res 93:101-28
Ruifrok, A C; Weil, M M; Thames, H D et al. (1998) Diurnal variations in the expression of radiation-induced apoptosis. Radiat Res 149:360-5
Powers, B E; Thames, H D; Gillette, S M et al. (1998) Volume effects in the irradiated canine spinal cord: do they exist when the probability of injury is low? Radiother Oncol 46:297-306
Ruifrok, A C; Weil, M M; Mason, K A et al. (1998) Induction of transforming growth factor alpha in irradiated mouse jejunum. Int J Radiat Oncol Biol Phys 42:1137-46
Ruifrok, A C; Mason, K A; Lozano, G et al. (1997) Spatial and temporal patterns of expression of epidermal growth factor, transforming growth factor alpha and transforming growth factor beta 1-3 and their receptors in mouse jejunum after radiation treatment. Radiat Res 147:1-12
Thames, H D; Ruifrok, A C; Mason, K A (1997) The effect of proliferative status and clonogen content on the response of mouse jejunal crypts to split-dose irradiation. Radiat Res 147:172-8

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