首页> 外文期刊>Hepato-gastroenterology. >A phase I trial of CPT-11 and S-1 combination chemotherapy in patients with metastatic colorectal cancer.
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A phase I trial of CPT-11 and S-1 combination chemotherapy in patients with metastatic colorectal cancer.

机译:CPT-11和S-1联合化疗在转移性结直肠癌患者中进行的I期临床试验。

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BACKGROUND/AIMS: To establish a safe and practical chemotherapeutic regimen using CPT-11 in combination with an oral 5FU derivative S-1 for patients with metastatic colorectal cancer, a phase I clinical trial was conducted in an outpatient setting. METHODOLOGY: Nine patients with metastatic colorectal cancer were enrolled. S-1 was administered at approved doses of 80 mg/body/day to eligible patients with a body surface area (BSA) of less than 1.25m2, 100 mg/body/day to those with a BSA of 1.25-1.5m2, and 120 mg/body/day to those with a BSA of more than 1.5m2, for 2 weeks followed by 1 week rest, comprising one treatment cycle of 3 weeks. CPT-11 was administered on day 8 of the S-1 cycle. The dose of CPT-11 was escalated from 60-120 mg/m2 by every 20 mg/m2 for every cohort consisting of at least 3 patients in order to define dose-limiting toxicity (DLT), maximal tolerated dose (MTD), and recommended dose (RD) in preparation for a phase II trial. RESULTS: In regard to the hematologic toxicity, a decreaseof WBC to less than grade 2 was observed in 2 patients until the dose was escalated to 100 mg/m2 of CPT-11, which delayed the treatment for 1 week in 1 patient. Regarding non-hematologic toxicity, fatigue and gastrointestinal toxicity, including anorexia and nausea/vomiting, at grades 1 and 2 were commonly observed throughout the dose levels. Diarrhea at grade 3 was observed at the 4th cycle of 100 mg/m2 CPT-11 in 2 of 3 patients, both of whom required hospitalization. All patients were able to complete more than 3 treatment cycles, and 1 patient at 80 mg/m2 of CPT-11 was able to receive 31 treatment cycles. Observed tumor responses included 1 partial response (PR), 2 moderate responses, 4 stable diseases, and 2 progressive diseases. Serum CEA level decreased in 7 of the 9 patients enrolled. CONCLUSIONS: These results suggest that this treatment regimen using CPT-11 in combination with oral S-1 therapy is a safe regimen in an outpatient setting and effective for patients with metastatic colorectal cancer. TheDLT is diarrhea at a MTD of 100 mg/m2 of CPT-11, and 80 mg/m2 CPT-11 is recommended for the next phase II trial.
机译:背景/目的:为了建立转移性结直肠癌患者使用CPT-11结合口服5FU衍生物S-1的安全实用的化疗方案,在门诊患者中进行了I期临床试验。方法:纳入9例转移性结直肠癌患者。 S-1的批准剂量为80毫克/人/天,适用于体表面积(BSA)小于1.25m2的合格患者; 100 mg /人/天的BSA为1.25-1.5m2的合格患者;以及对于BSA大于1.5平方米的人,每天120毫克/人/天,持续2周,然后休息1周,其中一个治疗周期为3周。在S-1周期的第8天给予CPT-11。对于至少由3名患者组成的队列,将CPT-11的剂量从60-120 mg / m2逐步提高到每20 mg / m2,以定义剂量限制毒性(DLT),最大耐受剂量(MTD)和建议剂量(RD),以准备进行II期试验。结果:关于血液学毒性,在2名患者中观察到WBC降至2级以下,直到剂量增加至CPT-11的100 mg / m2,这使1名患者的治疗延迟了1周。关于非血液学毒性,通常在整个剂量水平上观察到1级和2级的疲劳和胃肠道毒性,包括厌食和恶心/呕吐。 3例患者中有2例在第4周期100 mg / m2 CPT-11的第4级观察到腹泻,均需要住院。所有患者均能够完成3个以上的治疗周期,并且1个以80 mg / m2的CPT-11进行治疗的患者能够接受31个治疗周期。观察到的肿瘤反应包括1部分反应(PR),2中度反应,4稳定疾病和2进行性疾病。 9名患者中有7名血清CEA水平下降。结论:这些结果表明,使用CPT-11联合口服S-1疗法的这种治疗方案在门诊患者中是安全的方案,对转移性结直肠癌患者有效。在100 mg / m2的CPT-11的MTD下,DLT是腹泻,建议在下一个II期试验中使用80 mg / m2的CPT-11。

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