Fowler Jeffrey M, Brady William E, Grigsby Perry W, Cohn David E, Mannel Robert S, Rader Janet S
The Ohio State University, Gynecologic Oncology, M210 Starling-Loving Hall, 320 West Tenth Avenue, Columbus, OH 43210-1228, USA.
Gynecol Oncol. 2009 Mar;112(3):553-7. doi: 10.1016/j.ygyno.2008.11.026. Epub 2009 Jan 9.
The optimal treatment regimen for advanced stage endometrial carcinoma (EC) is yet to be established. The objective of this study was to evaluate the feasibility and toxicity of delivering sequential doxorubicin-cisplatin (AC) followed by whole abdomen irradiation (WAI).
Patients with stage III/IV EC with <2 cm residual disease were eligible. The treatment regimen included 3 cycles of AC (50 mg/m(2) each) followed by WAI plus para-aortic and/or true pelvic boost. Outcome objectives were feasibility of the regimen, acute toxicity and chronic irradiation toxicity monitored for at least one year after completing treatment.
Thirty-one patients were entered onto the study. Twenty-nine were evaluable for feasibility of the regimen, and 22 patients were evaluable for chronic radiation toxicity with a median follow-up of 21 months. Three patients (14%) experienced severe chronic toxicity including one treatment-related death. The five-year progression-free survival (PFS) and overall survival (OS) was 52.5% and 60.1% respectively.
The results from the first stage of this study found this regimen of sequential AC followed by WAI eligible for further study. Although toxicity was not excessive at the time of completion of the first stage, there was insufficient interest by the Gynecologic Oncology Group to continue study of this regimen; therefore, a conclusion regarding feasibility and chronic toxicity in an expanded cohort as initially intended is not possible. The risk of recurrence in advanced EC is sufficiently high that may warrant further investigation of sequential chemotherapy and WAI.
晚期子宫内膜癌(EC)的最佳治疗方案尚未确定。本研究的目的是评估序贯给予阿霉素-顺铂(AC)后进行全腹照射(WAI)的可行性和毒性。
符合条件的患者为Ⅲ/Ⅳ期EC且残留病灶<2 cm。治疗方案包括3个周期的AC(各50 mg/m²),随后进行WAI加腹主动脉旁和/或真骨盆区的增强照射。观察指标为该方案的可行性、急性毒性以及治疗完成后至少随访一年的慢性放射毒性。
31例患者进入本研究。29例可评估该方案的可行性,22例可评估慢性放射毒性,中位随访时间为21个月。3例患者(14%)出现严重慢性毒性,包括1例与治疗相关的死亡。五年无进展生存期(PFS)和总生存期(OS)分别为52.5%和60.1%。
本研究第一阶段的结果表明,这种序贯AC后进行WAI的方案适合进一步研究。尽管在第一阶段结束时毒性不过高,但妇科肿瘤学组对继续研究该方案兴趣不足;因此,无法按照最初设想得出关于扩大队列中该方案可行性和慢性毒性的结论。晚期EC的复发风险足够高,可能值得对序贯化疗和WAI进行进一步研究。