首页> 外文期刊>Oncology: International Journal of Cancer Research and Treatment >Modified CAPOX (capecitabine plus oxaliplatin) regimen every two weeks as second-line treatment in patients with advanced colorectal cancer previously treated with irinotecan-based frontline therapy: a multicenter phase II study.
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Modified CAPOX (capecitabine plus oxaliplatin) regimen every two weeks as second-line treatment in patients with advanced colorectal cancer previously treated with irinotecan-based frontline therapy: a multicenter phase II study.

机译:每两周修改的CAPOX(卡培他滨加奥沙利铂)方案作为二线治疗,用于先前已接受基于伊立替康的一线治疗的晚期大肠癌患者:一项多中心II期研究。

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BACKGROUND: To evaluate the efficacy and tolerance of capecitabine (CAP) given every other week and biweekly oxaliplatin (OX; modified CAPOX regimen) in patients with advanced colorectal cancer previously treated with irinote- can-based frontline chemotherapy. METHODS: Sixty-seven patients were enrolled; the median age was 62 years and 62 (92.5%) had a performance status (ECOG) of 0-1. OX and CAP were administered at the dose of 100 mg/m(2) on day 1 and 2,000 mg/m(2) on days 1-7, respectively, every 2 weeks. RESULTS: A total of 429 treatment cycles were administered. Grade 3/4 neutropenia and thrombocytopenia were observed in 4 (6%) and 2 (3%) patients, respectively. Febrile neutropenia complicated 1 treatment cycle. The main nonhematologic toxicities were grade 2/3 peripheral sensory neurotoxicity (10% of patients) and grade 3/4 diarrhea (7%). In an intention-to-treat analysis, 3 (4.5%) complete and 13 (19.4%) partial responses (overall response rate 24%) were observed. Seventeen (24.5%) patients had stable and 27 (40.3%) progressive disease. The median time to tumor progression and overall survival were 5 months and 11.3 months, respectively. CONCLUSIONS: The results indicate that the modified CAPOX regimen is safe and effective as salvage treatment in patients with advanced colorectal cancer who were previously treated with irinotecan-based frontline therapy.
机译:背景:评估每两周一次给予卡培他滨(CAP)和每两周一次奥沙利铂(OX;改良的CAPOX方案)的疗效和耐受性,这些患者先前接受过基于伊立替康的一线化疗。方法:67例患者入选。中位年龄为62岁,其中62位(92.5%)的工作状态(ECOG)为0-1。每2周分别在第1天和第1-7天分别以100 mg / m(2)和2,000 mg / m(2)的剂量给药OX和CAP。结果:总共进行了429个治疗周期。分别在4(6%)和2(3%)患者中观察到3/4级中性粒细胞减少和血小板减少。发热性中性粒细胞减少症使1个治疗周期复杂化。主要的非血液学毒性是2/3级周围感觉神经毒性(占患者的10%)和3/4级腹泻(占7%)。在意向性治疗分析中,观察到3例(4.5%)完全反应和13例(19.4%)部分反应(总体反应率为24%)。 17名(24.5%)患者病情稳定,而27名(40.3%)患者病情进展。肿瘤进展和中位生存时间的中位数分别为5个月和11.3个月。结论:结果表明,改良的CAPOX方案作为晚期结直肠癌患者的挽救治疗是安全有效的,这些患者先前曾接受过基于伊立替康的一线治疗。

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