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首页> 外文期刊>The British journal of cancer >Bevacizumab in combination with biweekly capecitabine and irinotecan, as first-line treatment for patients with metastatic colorectal cancer.
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Bevacizumab in combination with biweekly capecitabine and irinotecan, as first-line treatment for patients with metastatic colorectal cancer.

机译:贝伐单抗结合的半月刊卡培他滨和伊立替康,一线治疗转移性大肠癌患者癌症。

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BACKGROUND: Combination of capecitabine and irinotecan (XELIRI regimen) is an active and well tolerated treatment for metastatic colorectal cancer (mCRC). The aim of this study was to evaluate the efficacy and safety of this regimen in combination with bevacizumab (BV), as first-line treatment for mCRC. PATIENTS AND METHODS: A total of 46 consecutive patients received a combination of BV (5 mg kg(1), day 1), irinotecan (175 mg m(2), day 1) and capecitabine (1000 mg m(2) twice daily on day 2-8), every 2 weeks. Patients were treated until disease progression or unacceptable toxicity. The primary objective was to determine the progression-free survival (PFS) and safety profile. RESULTS: The overall response rate (ORR) was 67.4%, with a disease control rate (ORR+stable disease) of 93.5%. Median PFS and overall survival (OS) were 12.3 months (95% confidence interval (CI): 6.5-18.1 months) and 23.7 months (95% CI: 16.7-30.6 months), respectively. The most frequent grade 3/4 treatment-related adverse events were asthenia (7%), diarrhoea (7%), nausea (9%) and vomiting (7%). CONCLUSION: Bevacizumab combined with biweekly XELIRI is a highly active first-line regimen for mCRC treatment, showing encouraging PFS, ORR and OS with a good tolerability.
机译:背景:卡培他滨和组合伊立替康(XELIRI方案)是一个活跃的容忍治疗转移性大肠癌癌症(mCRC)。评估这个方案的有效性和安全性结合贝伐单抗(BV)一线治疗mCRC。方法:总共有46个病人收到BV的组合(5毫克公斤(1),第一天),伊立替康(175毫克(2),第一天)和卡培他滨每天两次(1000毫克(2)2 - 8天),每2周。发展或不可接受的毒性。目标是确定无进展生存(PFS)和安全性。总体响应率(ORR)为67.4%,与疾病控制速率(奥尔+稳定的疾病)93.5%。12.3个月(95%可信区间(CI):6.5 - -18.1个月和23.7个月(95%置信区间CI:分别为16.7 -30.6个月)。频繁的3/4级治疗相关的不良事件是无力(7%)、腹泻(7%)、恶心(9%)、呕吐(7%)。结合两周一次的XELIRI是一个高度活跃一线方案mCRC治疗,显示鼓励PFS,或者用好和操作系统耐受性。

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