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顺铂和5-氟尿嘧啶在晚期和复发性胃癌中的序列依赖性

Sequence-dependence of cisplatin and 5-fluorouracil in advanced and recurrent gastric cancer.

作者信息

Koizumi Wasaburo, Kurihara Minoru, Hasegawa Koichi, Chonan Akimichi, Kubo Yasuhiko, Maekawa Ryuichiro, Iwasaki Ryozo, Sasai Tadashi, Fukuyama Yoshio, Ishikawa Kunitsugu, Miyoshi Kazuo, Yasutake Koichi, Hayakawa Makoto

机构信息

Department of Gastroenterology, Higashi Hospital, Kitasato University, School of Medicine, 2-1-1 Asamizodai, Sagamihara-shi, Kanagawa Prefecture 228-8520, Japan.

出版信息

Oncol Rep. 2004 Sep;12(3):557-61.

Abstract

This randomized controlled clinical trial was designed to compare the safety and effectiveness of different sequences of treatment with cisplatin (CDDP) and 5-fluorouracil (5-FU) in patients with unresectable advanced and post-operative recurrent gastric cancer. Patients with unresectable advanced or post-operative recurrent gastric cancer were randomly assigned by a registration center to group A or B. Group A received CDDP (80 mg/m(2)) as a continuous 2-h intravenous infusion on day 1 and 5-FU (700 mg/m(2)) as a continuous intravenous infusion on days 2-5. Group B was given 5-FU (700 mg/m(2)) as a continuous intravenous infusion on days 1-4, followed by CDDP (80 mg/m(2)) as a continuous 2-h intravenous infusion on day 5. Each course of chemotherapy was repeated every 28 days. A total of 74 patients were enrolled. One patient died accidentally, and 5 could not be evaluated. Response was assessable in 68 patients. The response rate was 31.3% (10/32) in group A as compared with 13.9% (5/36) in group B. Although the response rate was higher in Group A, the difference was not significant (p=0.085). The response rate in patients with diffuse type tumors was significantly lower in group B. There was no difference between the groups in response among patients with intestinal type tumors. The median overall survival was 239 and 174 days and time to progression was 175 and 140 days in group A and group B, respectively. Although there were trends toward longer survival and time to progression in group A, the differences between the groups were not statistically significant. There was also no difference in the type or incidence of adverse reactions. The results of this controlled study indicate that the overall response rate was slightly but not significantly higher in patients who received CDDP before 5-FU. Among patients with diffuse type tumors, the response rate was significantly lower when 5-FU was administered before CDDP. Our results suggest that CDDP should be given before 5-FU in patients with gastric cancer when treated with a combination of CDDP and 5-FU.

摘要

这项随机对照临床试验旨在比较顺铂(CDDP)和5-氟尿嘧啶(5-FU)不同治疗顺序在不可切除的晚期及术后复发性胃癌患者中的安全性和有效性。不可切除的晚期或术后复发性胃癌患者由一个登记中心随机分配至A组或B组。A组在第1天接受顺铂(80mg/m²)持续2小时静脉输注,在第2 - 5天接受5-氟尿嘧啶(700mg/m²)持续静脉输注。B组在第1 - 4天接受5-氟尿嘧啶(700mg/m²)持续静脉输注,在第5天接受顺铂(80mg/m²)持续2小时静脉输注。每28天重复一个化疗疗程。共纳入74例患者。1例患者意外死亡,5例无法评估。68例患者可评估疗效。A组的有效率为31.3%(10/32),B组为13.9%(5/36)。虽然A组的有效率较高,但差异无统计学意义(p = 0.085)。弥漫型肿瘤患者中,B组的有效率显著较低。肠型肿瘤患者中,两组间的疗效无差异。A组和B组的中位总生存期分别为239天和174天,疾病进展时间分别为175天和140天。虽然A组有生存时间和疾病进展时间更长的趋势,但两组间差异无统计学意义。不良反应的类型和发生率也无差异。这项对照研究的结果表明,5-氟尿嘧啶之前接受顺铂治疗的患者总体有效率略高但无显著差异。在弥漫型肿瘤患者中,5-氟尿嘧啶在顺铂之前给药时有效率显著较低。我们的结果提示,胃癌患者联合使用顺铂和5-氟尿嘧啶治疗时,顺铂应在5-氟尿嘧啶之前给药。

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