The prevalence and severity of late effects in normal rat duodenum following intraoperative irradiation

In humans, a portion of the duodenum is often at risk for radiation-induced complications following intraoperative radiation therapy for pancreatic carcinoma. To determine experimentally the prevalence and severity of late effects in the normal mammalian duodenum, 190 rats received single doses of 0...

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Published inInternational journal of radiation oncology, biology, physics Vol. 18; no. 4; pp. 841 - 848
Main Authors Poulakos, Lawrence, Elwell, James H., Osborne, James W., Urdaneta, Luis F., Hauer-Jensen, Martin, Vigliotti, Antonio P., Hussey, David H., Summers, Robert W.
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.04.1990
Elsevier
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Summary:In humans, a portion of the duodenum is often at risk for radiation-induced complications following intraoperative radiation therapy for pancreatic carcinoma. To determine experimentally the prevalence and severity of late effects in the normal mammalian duodenum, 190 rats received single doses of 0, 15, 20, 25, 30, or 40 Gy orthovoltage X rays to temporarily exteriorized 3 cm circumferential segments of duodenum. The animals were killed 2, 6, 8, or 10 months later. Actuarial survival, change in body weight, and a radiation injury score based on eight histopathologic alterations were used as endpoints. Epithelial atypia, intestinal wall fibrosis, serosal thickening, and vascular sclerosis were the dominant histopathologic alterations at all dose levels throughout the 10-month observation period. The prevalence and severity of histologic radiation injury showed sigmoidal dose-response relationships with the plateaus starting at 20 Gy. Doses of 20 Gy or greater also resulted in a substantial loss of body weight and a high level of early deaths (20–80 days). All endpoints indicate that intraoperative doses of 20 Gy or greater are associated with unacceptable risks of late and irreversible complications.
ISSN:0360-3016
1879-355X
DOI:10.1016/0360-3016(90)90406-A