Yamada Yasuhide, Ohtsu Atsushi, Boku Narikazu, Miyata Yoshinori, Shimada Yasuhiro, Doi Toshihiko, Muro Kei, Muto Manabu, Hamaguchi Tetsuya, Mera Kiyomi, Yano Tomonori, Tanigawara Yusuke, Shirao Kuniaki
Gastrointestinal Oncology Division, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.
Jpn J Clin Oncol. 2006 Apr;36(4):218-23. doi: 10.1093/jjco/hyl020.
Infusional fluorouracil (5-FU) and leucovorin (LV) with oxaliplatin is one of the current standard regimens for the treatment of patients with metastatic colorectal cancer. Weekly bolus 5-FU with high-dose LV (Roswell Park Memorial Institute Regimen: RPMI) is the most commonly used regimen in Japan. The objectives of this study were to determine the recommended dose (RD) of RPMI combined with oxaliplatin and to evaluate the toxicity and efficacy at the RD.
The subjects were 18 patients with metastatic colorectal cancer. Oxaliplatin (85 mg/m2) was given intravenously over 2 h on days 1 and 15 with l-LV (250 mg/m2) given intravenously over 2 h and 5-FU as an intravenous bolus on days 1, 8, and 15. This treatment was repeated every 4 weeks. The dose of 5-FU was escalated from 400 mg/m2 (level 1) to 500 mg/m2 (level 2).
A total of 14 patients received level 1, and 4 received level 2. Three of the patients had dose-limiting toxicity (DLT) in cycle 1 of level 2 (grade 3 thrombocytopenia, grade 4 neutropenia and grade 2 neutropenia in one patient each), requiring that treatment was delayed for longer than 7 days. None of the 14 patients given level 1 had DLT or grade 3 or 4 gastrointestinal toxicity. Sensory neuropathy occurred in all patients. Objective response rates were 61% in the 18 patients studied and 64% at level 1. The median time to progression was 171 days, and the median overall survival time was 603 days in the 18 patients studied.
Oxaliplatin (85 mg/m2) with weekly bolus 5-FU (400 mg/m2) and high-dose l-LV (250 mg/m2) is recommended for further phase III studies in patients with metastatic colorectal cancer.
氟尿嘧啶(5-FU)持续输注联合亚叶酸钙(LV)及奥沙利铂是目前治疗转移性结直肠癌患者的标准方案之一。每周大剂量LV推注5-FU(罗斯韦尔帕克纪念研究所方案:RPMI)是日本最常用的方案。本研究的目的是确定RPMI联合奥沙利铂的推荐剂量(RD),并评估该RD下的毒性和疗效。
研究对象为18例转移性结直肠癌患者。奥沙利铂(85mg/m²)在第1天和第15天静脉滴注2小时,左亚叶酸钙(250mg/m²)静脉滴注2小时,5-FU在第1、8和15天静脉推注。每4周重复一次该治疗。5-FU的剂量从400mg/m²(1级)逐步增加至500mg/m²(2级)。
共有14例患者接受1级治疗,4例接受2级治疗。2级治疗的第1周期中有3例患者出现剂量限制性毒性(DLT)(分别为1例3级血小板减少、1例4级中性粒细胞减少和1例2级中性粒细胞减少),需要将治疗延迟超过7天。接受1级治疗的14例患者均未出现DLT或3/4级胃肠道毒性。所有患者均出现感觉神经病变。在18例研究患者中,客观缓解率为61%,1级治疗时为64%。在18例研究患者中,疾病进展的中位时间为171天,总生存时间的中位值为603天。
推荐奥沙利铂(85mg/m²)联合每周一次的5-FU推注(400mg/m²)及大剂量左亚叶酸钙(250mg/m²)用于转移性结直肠癌患者的进一步III期研究。