Rich T A, Ajani J A, Morrison W H, Ota D, Levin B
Department of Radiotherapy, University of Texas M.D. Anderson Cancer Center, Houston 77030.
Radiother Oncol. 1993 Jun;27(3):209-15. doi: 10.1016/0167-8140(93)90076-k.
Chemoradiation therapy for anal cancer was carried out in 58 patients using low-dose, continuous infusion of 5-fluorouracil (5-FU) with or without continuous infusion of cisplatin (cDDP) and external beam irradiation (chemoXRT). Thirty-nine patients received 5-FU chemoXRT resulting in a local control rate of 50% in those receiving a total dose of < 45 Gy, 73% for those receiving 50-54 Gy, and 83% for those receiving > 60 Gy. The actuarial local control rate at 2 years was 77% after chemoXRT alone; overall local control was 67% at 5 years. In 18 patients receiving 5-FU plus cisplatin with radiation doses of 54-55 Gy, actuarial local control was 85% at 2 years. Fifteen patients failed chemoXRT, 13 of whom had abdominoperineal resection for salvage; the overall local control rate was 93% (54/58). The actuarial survival at 5 years was 81% for the 5-FU chemoXRT group and 94% at 2 years for the 5-FU plus cisplatin chemoXRT group; median follow-up was 54 and 20 months, respectively. Diarrhea and nausea were the most frequent early reactions and were ameliorated by limiting the duration of chemotherapy to 5 days/week and by using XRT techniques to exclude the small bowel from the radiation portal. Serious late radiation complications have not been observed and may be related to XRT fractionation and the use of protracted chemotherapy infusion. The absence of late morbidity coupled with the high local control rate by the use of this chemoXRT program is an area to investigate for improving the therapeutic ratio for the treatment of anal cancers.
对58例肛管癌患者实施了放化疗,采用低剂量持续输注5-氟尿嘧啶(5-FU),联合或不联合持续输注顺铂(cDDP)及外照射(化疗联合放疗)。39例患者接受了5-FU化疗联合放疗,总剂量<45 Gy的患者局部控制率为50%,接受50-54 Gy的患者为73%,接受>60 Gy的患者为83%。单纯化疗联合放疗后2年的精算局部控制率为77%;5年时总体局部控制率为67%。18例接受5-FU加顺铂且放疗剂量为54-55 Gy的患者,2年精算局部控制率为85%。15例患者化疗联合放疗失败,其中13例接受了腹会阴联合切除术进行挽救;总体局部控制率为93%(54/58)。5-FU化疗联合放疗组5年精算生存率为81%,5-FU加顺铂化疗联合放疗组2年精算生存率为94%;中位随访时间分别为54个月和20个月。腹泻和恶心是最常见的早期反应,通过将化疗时间限制在每周5天以及采用放疗技术将小肠排除在照射野之外可使其得到缓解。尚未观察到严重的晚期放疗并发症,这可能与放疗分割方式及采用延长的化疗输注有关。通过该化疗联合放疗方案未出现晚期并发症且局部控制率高,这是一个值得研究以提高肛管癌治疗比的领域。