Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Am J Clin Oncol. 2010 Feb;33(1):56-60. doi: 10.1097/COC.0b013e31819fe216.
There is no universally confirmed standard chemotherapeutic regimen for advanced gastric cancer (AGC). The aim of this study was to investigate the efficacy and safety of combined biweekly irinotecan and monthly cisplatin treatments of patients with AGC. The primary end point was progression-free survival.
AGC patients with or without measurable lesions received 70 mg/m2 irinotecan on days 1 and 15, and 80 mg/m2 cisplatin on day 1 every 4 weeks.
Of 40 enrolled patients, 21 patients had measurable disease. With a median follow-up duration of 35 weeks, the median progression-free survival and overall survival were 2.2 months and 8.0 months, respectively. The progression-free survival rate at 6 months was 30.0%. The most common adverse event of grade 3 to 4 was neutropenia (32.5%). Grade 3 diarrhea was observed in 2 patients (5.0%). There was no treatment-related death.
Current combined biweekly irinotecan and monthly cisplatin treatment did not show activity comparable with other active regimens in AGC.
晚期胃癌(AGC)目前尚无被广泛认可的标准化疗方案。本研究旨在探讨每周两次伊立替康联合每月顺铂治疗 AGC 患者的疗效和安全性。主要终点为无进展生存期。
入组的 AGC 患者,无论是否存在可测量病灶,均接受伊立替康 70 mg/m2 静滴,于第 1 天和第 15 天给药,顺铂 80 mg/m2 静滴,于第 1 天给药,每 4 周 1 次。
40 例入组患者中,21 例存在可测量病灶。中位随访时间 35 周时,中位无进展生存期和总生存期分别为 2.2 个月和 8.0 个月,6 个月无进展生存率为 30.0%。最常见的 3 级至 4 级不良事件为中性粒细胞减少(32.5%)。2 例(5.0%)患者出现 3 级腹泻。无治疗相关死亡。
目前每周两次伊立替康联合每月顺铂的治疗方案在晚期胃癌中的疗效并不优于其他有效方案。