Langberg C W, Waldron J A, Baker M L, Hauer-Jensen M
Department of Surgery, University of Arkanasas for Medical Science, Little Rock.
Cancer. 1994 May 15;73(10):2663-8. doi: 10.1002/1097-0142(19940515)73:10<2663::aid-cncr2820731031>3.0.co;2-c.
Late normal tissue reactions generally are believed to be independent of treatment time. However, previous studies suggest a relationship between acute mucosal injury and development of intestinal obstruction and enterocutaneous fistula formation. Thus, the pathogenesis of late intestinal complications may be complex, and mucosal cell proliferation during treatment may be important. This study assessed the influence of overall radiation treatment time on development of intestinal injury and complications after localized fractionated irradiation of rat ilium.
Ninety-four male rats underwent orchiectomy, and a loop of small intestine was transposed to the scrotum. Orthovoltage irradiation was administered to the transposed, but functionally intact, intestine using 9 fractions of 5.6 Gy with interfraction intervals of 24, 48, or 72 hours. The animals were observed for complications and killed in groups 2 and 26 weeks after irradiation for assessment of injury. Incidence of intestinal complications and quantitative and semiquantitative histopathologic assessment of injury were used as endpoints.
Increasing total treatment time by extending interfraction intervals from 24 to 48 hours significantly reduced radiation injury and the incidence of intestinal complications. Differences in mucosal and fibrotic changes were most prominent. No significant differences were found between groups with interfraction intervals of 48 and 72 hours.
Overall treatment time significantly influenced development of chronic radiation enteropathy. Thus, rapidly proliferating cells, as found in the intestinal mucosa, appear to be involved in the pathogenesis of intestinal complications. This probably represents consequential damage secondary to disruption of mucosal integrity.
一般认为晚期正常组织反应与治疗时间无关。然而,先前的研究表明急性黏膜损伤与肠梗阻及肠皮肤瘘形成之间存在关联。因此,晚期肠道并发症的发病机制可能较为复杂,治疗期间黏膜细胞增殖可能起重要作用。本研究评估了大鼠髂骨局部分次照射后,总放疗时间对肠道损伤及并发症发生发展的影响。
94只雄性大鼠接受睾丸切除术,将一段小肠移位至阴囊。对移位但功能完整的小肠进行深部X线照射,分9次给予5.6 Gy,每次照射间隔24、48或72小时。观察动物并发症情况,并在照射后2周和26周分批处死动物以评估损伤。以肠道并发症发生率及损伤的定量和半定量组织病理学评估作为观察终点。
将分次照射间隔从24小时延长至48小时以增加总治疗时间,可显著减轻放射性损伤及肠道并发症的发生率。黏膜和纤维化改变的差异最为显著。分次照射间隔为48小时和72小时的组间未发现显著差异。
总治疗时间显著影响慢性放射性肠炎的发生发展。因此,如在肠黏膜中发现的快速增殖细胞似乎参与了肠道并发症的发病机制。这可能代表黏膜完整性破坏继发的继发性损伤。