Park Se Hoon, Choi Eun Young, Bang Soo-Mee, Cho Euk Kyung, Lee Jae Hoon, Shin Dong Bok, Ki Lee Woon, Chung Min
Division of Hematology and Oncology, Department of Internal Medicine, Gachon Medical School Gil Medical Center, Incheon, South Korea.
Anticancer Drugs. 2005 Jul;16(6):621-5. doi: 10.1097/00001813-200507000-00005.
We conducted a phase II study to assess the efficacy and tolerability of irinotecan and cisplatin as salvage chemotherapy in patients with advanced gastric adenocarcinoma, progressing after both 5-fluorouracil (5-FU)- and taxane-containing regimen. Patients with measurable metastatic gastric cancer, progressive after previous chemotherapy that consisted either of a 5-FU-based regimen followed by second-line chemotherapy containing taxanes or a 5-FU and taxane combination were treated with irinotecan and cisplatin. Irinotecan 70 mg/m(2) was administered on day 1 and day 15; cisplatin 70 mg/m(2) was administered on day 1. Treatment was repeated every 4 weeks. For 28 patients registered, a total of 94 chemotherapy cycles were administered. The patients' median age was 51 years and 27 (96%) had an ECOG performance status of 1 or below. In an intent-to-treat analysis, seven patients (25%) achieved a partial response, which maintained for 6.3 months (95% confidence interval 6.2-6.4 months). The median progression-free and overall survival were 3.5 and 5.6 months, respectively. Major toxic effects included nausea, diarrhea and neurotoxicity. Although there was one possible treatment-related death, toxicity profiles were generally predictable and manageable. We conclude that irinotecan and cisplatin is an active combination for patients with metastatic gastric cancer in whom previous chemotherapy with 5-FU and taxanes has failed.
我们开展了一项II期研究,以评估伊立替康和顺铂作为挽救性化疗方案,用于晚期胃腺癌患者的疗效和耐受性,这些患者在含5-氟尿嘧啶(5-FU)和紫杉烷的方案治疗后病情进展。可测量的转移性胃癌患者,在先前化疗后病情进展,先前化疗方案包括基于5-FU的方案后序贯含紫杉烷的二线化疗,或5-FU与紫杉烷联合化疗,这些患者接受伊立替康和顺铂治疗。伊立替康70mg/m²在第1天和第15天给药;顺铂70mg/m²在第1天给药。每4周重复治疗。对于登记的28例患者,共进行了94个化疗周期。患者的中位年龄为51岁,27例(96%)的东部肿瘤协作组(ECOG)体能状态为1或更低。在意向性分析中,7例患者(25%)达到部分缓解,缓解持续6.3个月(95%置信区间6.2 - 6.4个月)。中位无进展生存期和总生存期分别为3.5个月和5.6个月。主要毒性反应包括恶心、腹泻和神经毒性。虽然有1例可能与治疗相关的死亡,但毒性特征通常是可预测和可控制的。我们得出结论,对于先前接受5-FU和紫杉烷化疗失败的转移性胃癌患者,伊立替康和顺铂是一种有效的联合方案。