Johnstone P A, Sprague M, DeLuca A M, Bacher J D, Hampshire V A, Terrill R E, Kinsella T J, Sindelar W F
Radiation Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Int J Radiat Oncol Biol Phys. 1994 Jul 30;29(5):1015-25. doi: 10.1016/0360-3016(94)90397-2.
The effects of intraoperative radiotherapy +/- external beam radiotherapy on prosthetic vascular grafts were investigated in a canine model.
In 1986 and 1987, 30 adult beagles underwent laparotomy with transection and segmental resection of the infrarenal aorta followed by immediate reconstruction with a prosthetic graft. Intraoperative radiotherapy at varying doses from 0-30 Gy was then administered to all animals. Half of the dogs received 36 Gy external beam radiotherapy in 10 fractions postoperatively. Animals were sacrificed and necropsied at predetermined intervals and as clinically indicated to assess early (< or = 6 months) and late (> 6 months) effects to the vascular graft and surrounding normal tissue.
Histopathologic analyses of irradiated vascular structures were performed and correlations were made with the clinical outcome. The most frequent early clinical toxicity was graft thrombosis, occurring in 7 of 10 animals followed for < or = 6 months. Early graft thrombus formation appeared unrelated to radiotherapy dose and probably represented a technical surgical complication. Anastomotic stenosis of varying severity occurred in most animals followed > 6 months. Late (> 6 months) graft stenosis was correlated with intraoperative radiotherapy dose. At < or = 20 Gy of intraoperative irradiation, 3 of 14 animals developed late graft occlusion; at > 25 Gy, five of six animals developed late occlusion. On histopathologic review, increasing intraoperative dose and increasing total radiotherapy dose (intraoperative+external beam) appeared to correspond with increasing severity of graft changes seen after 6 months of follow-up.
Thrombus formation is a frequent early complication of vascular graft placement of the infrarenal aorta in our beagle dog model. Intraoperative doses up to 20 Gy appear to contribute minimally to late graft occlusion, while doses > or = 25 Gy contribute to late occlusion with high likelihood. Both intraoperative dose and total radiotherapy dose correlated with late graft occlusion, and with histopathologic changes in the graft and anastomoses.
在犬模型中研究术中放疗±外照射放疗对人工血管移植物的影响。
1986年和1987年,30只成年比格犬接受剖腹手术,横断并节段切除肾下腹主动脉,随后立即用人工移植物进行重建。然后对所有动物给予0 - 30 Gy不同剂量的术中放疗。一半的犬在术后接受10次分割的36 Gy外照射放疗。在预定的时间间隔并根据临床指征对动物实施安乐死并进行尸检,以评估对血管移植物和周围正常组织的早期(≤6个月)和晚期(>6个月)影响。
对照射后的血管结构进行组织病理学分析,并与临床结果进行关联。最常见的早期临床毒性是移植物血栓形成,在随访≤6个月的10只动物中有7只出现。早期移植物血栓形成似乎与放疗剂量无关,可能是一种手术技术并发症。大多数随访>6个月的动物出现不同程度的吻合口狭窄。晚期(>6个月)移植物狭窄与术中放疗剂量相关。术中照射剂量≤20 Gy时,14只动物中有3只出现晚期移植物闭塞;剂量>25 Gy时,6只动物中有5只出现晚期闭塞。组织病理学检查显示,术中剂量增加和总放疗剂量(术中+外照射)增加似乎与随访6个月后移植物变化的严重程度增加相对应。
在我们的比格犬模型中,血栓形成是肾下腹主动脉血管移植物置入常见的早期并发症。术中剂量高达20 Gy似乎对晚期移植物闭塞的影响最小,而剂量≥25 Gy则很可能导致晚期闭塞。术中剂量和总放疗剂量均与晚期移植物闭塞以及移植物和吻合口的组织病理学变化相关。