Turrisi A T, Glover D J, Mason B A
Department of Radiation Therapy, Hospital of the University of Pennsylvania, Philadelphia 19104.
Int J Radiat Oncol Biol Phys. 1988 Jul;15(1):183-7. doi: 10.1016/0360-3016(88)90364-1.
From July 1984 through March 1987 23 patients with small cell lung cancer have entered a trial at the University of Pennsylvania. Concurrent Platinum (DDP) Etoposide (VP-16) chemotherapy and twice-daily, 150 cGy radiotherapy to a total dose of 4500 cGy in 3 weeks was used. Besides the twice-daily radiotherapy, multiple field arrangements attempted to minimize normal tissue exposure while concentrating on the target volume. Sophisticated CT-assisted treatment planning employing beams-eye-view technology was used. Esophagitis occurred in 73% (13% severe); hematologic toxicity occurred in 65% (17% WBC less than 1000). Response--100% in pure small cell carcinoma, 91% overall. Median follow-up is 22 months with an actuarial projection of 56% 2-year survival. Median survival is not yet reached. This is a highly effective therapy with substantive but tolerable toxicity. Accrual and follow-up continues. This is a preliminary report. We expect 30 patients before closing the study. A parallel study is underway in the Eastern Cooperative Oncology Group, with a randomized prospective trial in the design stage.
从1984年7月至1987年3月,23例小细胞肺癌患者参加了宾夕法尼亚大学的一项试验。采用顺铂(DDP)依托泊苷(VP - 16)同步化疗,以及每天两次、每次150 cGy的放疗,3周内总剂量达4500 cGy。除了每天两次的放疗外,多野照射方案在集中于靶体积的同时尽量减少正常组织的照射。采用了运用射野方向观技术的先进CT辅助治疗计划。食管炎发生率为73%(13%为重度);血液学毒性发生率为65%(17%白细胞计数低于1000)。缓解率——纯小细胞癌为100%,总体为91%。中位随访时间为22个月,2年生存率的精算预测为56%。中位生存期尚未达到。这是一种高效的治疗方法,毒性虽大但可耐受。病例积累和随访仍在继续。这是一份初步报告。我们预计在结束研究前有30例患者。东部肿瘤协作组正在进行一项平行研究,一项随机前瞻性试验正处于设计阶段。