Modifying Normal Tissue Damage Postirradiation
- 1 February 2002
- journal article
- Published by Radiation Research Society in Radiation Research
- Vol. 157 (2) , 204-223
- https://doi.org/10.1667/0033-7587(2002)157[0204:mntdp]2.0.co;2
Abstract
Stone, H. B., McBride, W. H. and Coleman, C. N. Modifying Normal Tissue Damage Postirradiation. Report of a Workshop Sponsored by the Radiation Research Program, National Cancer Institute. Radiat. Res. 157, 204–223 (2002). Late effects that develop in normal tissues adjacent to the tumor site in the months to years after radiotherapy can reduce the quality of life of cancer survivors. They can be dose-limiting and debilitating or life-threatening. There is now evidence that some late effects may be preventable or partially reversible. A workshop, “Modifying Normal Tissue Damage Postirradiation”, was sponsored by the Radiation Research Program of the National Cancer Institute to identify the current status of and research needs and opportunities in this area. Mechanistic, genetic and physiological studies of the development of late effects are needed and will provide a rational basis for development of treatments. Interdisciplinary teams will be needed to carry out this research, including pathologists, physiologists, geneticists, molecular biologists, experts in functional imaging, wound healing, burn injury, molecular biology, and medical oncology, in addition to radiation biologists, physicists and oncologists. The participants emphasized the need for developing and choosing appropriate models, and for radiation dose–response studies to determine whether interventions remain effective at the radiation doses used clinically. Both preclinical and clinical studies require long-term follow-up, and easier-to-use, more objective clinical scoring systems must be developed and standardized. New developments in biomedical imaging should provide useful tools in all these endeavors. The ultimate goals are to improve the quality of life and efficacy of treatment for cancer patients treated with radiotherapy.Keywords
This publication has 101 references indexed in Scilit:
- Genotype–phenotype relationship in inflammatory bowel diseaseEuropean Journal of Internal Medicine, 2000
- Chemokines and CD40 expression in human fibroblastsEuropean Journal of Immunology, 2000
- TGF-beta1-mediated alterations of rat lung fibroblast differentiation resulting in the radiation-induced fibrotic phenotypeInternational Journal of Radiation Biology, 2000
- Plasma transforming growth factor-?1 level before radiotherapy correlates with long term outcome of patients with lung carcinomaCancer, 1999
- Cutaneous Wound HealingNew England Journal of Medicine, 1999
- Do acute mucosal reactions lead to consequential late reactions in patients with head and neck cancer?Radiotherapy and Oncology, 1999
- Bilateral lymphocytic alveolitis: a common reaction after unilateral thoracic irradiationEuropean Respiratory Journal, 1999
- From wound to scarBurns, 1996
- The Functional Role of the ELR Motif in CXC Chemokine-mediated AngiogenesisJournal of Biological Chemistry, 1995
- Rat mammary carcinoma cells secrete active collagenase and activate latent enzyme in the stroma via plasminogen activatorInternational Journal of Cancer, 1981