Byfield J E, Sharp T R, Frankel S S, Tang S G, Callipari F B
J Clin Oncol. 1984 May;2(5):406-13. doi: 10.1200/JCO.1984.2.5.406.
Eighteen patients with advanced epithelial cancers of the head and neck region were studied for their tolerance and response to combined cycles of 120-hour infused 5-fluorouracil (5-FU) and external-beam radiation therapy. 5-FU infusions were given under conditions where radiosensitization would be expected at the higher infusion doses. Coincident radiation treatments were given as four sequential daily fractions of 250 rad each administered during days 1 through 4 of each five-day infusion cycle. The patients were rested for at least nine days after each cycle or longer until toxicity was resolved. The regimen was then repeated in each patient for a total of five treatment cycles. Thereafter therapy was consolidated, usually by boost radiation without drug. In sequential patient subsets the infusion load was progressively escalated in a phase I format. The complete response rate for stage IV patients was 75% with survival benefit compared to prior results. 5-FU dose-dependent combined modality loco-regional toxicity was demonstrated without significant enhancement of systemic toxicity of any form; 5-FU dose-dependent enhanced responsiveness and survival benefit is also suggested. Further scheduling and response studies of 5-FU under radiosensitizing conditions appear warranted.
对18例晚期头颈部上皮癌患者进行了研究,观察他们对120小时持续输注5-氟尿嘧啶(5-FU)与外照射放疗联合周期的耐受性和反应。5-FU输注在较高输注剂量下预期会产生放射增敏作用的条件下进行。同步放疗在每个五天输注周期的第1至4天进行,每天分4次给予,每次250拉德。每个周期后患者休息至少9天或更长时间,直到毒性消退。然后在每位患者中重复该方案,共进行五个治疗周期。此后通常通过加量放疗而不使用药物来巩固治疗。在连续的患者亚组中,输注负荷以I期模式逐步增加。IV期患者的完全缓解率为75%,与先前结果相比有生存获益。证实了5-FU剂量依赖性联合治疗局部区域毒性,且未显著增强任何形式的全身毒性;还提示了5-FU剂量依赖性增强反应性和生存获益。在放射增敏条件下对5-FU进行进一步的给药方案和反应研究似乎是必要的。