Abstract
Radiation therapy is an effective means of killing tumor cells, although this effectiveness is tempered by limitations of the normal tissue to the adverse effects of radiation. An excellent example of this is radiation treatment for thoracic tumors, in particular, lung cancers. Despite advances in the technical delivery of radiation by three-dimensional (3D) planning via computed tomography (CT), radiation-induced injury to normal lung tissue still occurs in a large proportion of treated patients. The primary endpoints for radiation-induced pulmonary toxicity include early onset pneumonitis and late onset fibrosis. A significant amount of research has produced some insight into the mechanism(s) behind this injury. This knowledge has provided potential targets for drug development that could improve the therapeutic ratio for radiation by reducing both early and late toxicity. In this article, we review and update the pathologic mechanisms underlying radiation-induced lung injury as well as potential treatments, with particular interest in cell adhesion molecules and inflammation.
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Willey, C.D., Hallahan, D.E. (2008). Inflammation and Cell Adhesion Molecules are Involved in Radiation-Induced Lung Injury. In: Rubin, P., Constine, L.S., Marks, L.B., Okunieff, P. (eds) Late Effects of Cancer Treatment on Normal Tissues. Medical Radiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-49070-8_4
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DOI: https://doi.org/10.1007/978-3-540-49070-8_4
Publisher Name: Springer, Berlin, Heidelberg
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