首页> 外文期刊>Journal of Cancer Therapy >A Multicenter Cohort Study for XELOX (Capecitabine, Leucovorin plus Oxaliplatin) Therapy as First-Line Treatment in Elderly Patients with Unresectable Colorectal Cancer
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A Multicenter Cohort Study for XELOX (Capecitabine, Leucovorin plus Oxaliplatin) Therapy as First-Line Treatment in Elderly Patients with Unresectable Colorectal Cancer

机译:XELOX(卡培他滨,白细胞素加奥沙利铂)治疗一线治疗老年不可切除结直肠癌患者的多中心队列研究

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Oxaliplatin-based chemotherapy with bevacizumab is now widely used for colorectal cancer patients. This study evaluated the efficacy and tolerability of XELOX (capecitabine + oxaliplatin + leucovorin combined) therapy with or without bevacizumab in elderly patients. One hundred and seven patients, consisting of 52 elderly (>70 years of age) and 55 non-elderly, with unresectable colorectal cancer were enrolled in this multicenter cooperative group study using a database between October 2009 and March 2012. We evaluated the outcomes in terms of the median time to treat failure (TTF), overall response rate (ORR), disease control rate (DCR) and tolerability in both age groups. The median TTF for the XELOX + bevacizumab regimen was 7.1 months in the non-elderly group and 8.1 months in the elderly group (p = 0.838). There was no significant difference in TTF between the two groups. The ORR and DCR in the non-elderly group were 30.8% and 73.1%, respectively. In the elderly group, the ORR was 40.0% and the overall DCR was 90.0%. No severe or uncontrollable adverse events were observed in the two groups. These data indicated that the XELOX chemotherapy with or without bevacizumab has an equivalent efficacy in both groups, without increasing the adverse events even in the elderly population.
机译:基于奥沙利铂的贝伐单抗化疗目前已广泛用于结直肠癌患者。这项研究评估了在有或没有贝伐单抗的情况下,老年患者使用XELOX(卡培他滨+奥沙利铂+亚叶酸钙联合治疗)的疗效和耐受性。这项多中心合作小组研究使用数据库在2009年10月至2012年3月之间纳入了107例患者,其中包括52例老年(> 70岁以上)和55例非老年性不可切除的结直肠癌。两个年龄组的中位治疗失败时间(TTF),总体缓解率(ORR),疾病控制率(DCR)和耐受性的术语。 XELOX +贝伐单抗方案的中位TTF在非老年组为7.1个月,在老年组为8.1个月(p = 0.838)。两组之间的TTF没有显着差异。非老年人组的ORR和DCR分别为30.8%和73.1%。老年组的ORR为40.0%,总DCR为90.0%。两组均未观察到严重或无法控制的不良事件。这些数据表明,有或没有贝伐单抗的XELOX化疗在两组中具有相同的疗效,即使在老年人群中也不会增加不良事件。

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