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Efficacy and Toxicity of Bevacizumab on Combination with Chemotherapy in Different Lines of Treatment for Metastatic Colorectal Carcinoma

机译:贝伐单抗联合化疗在转移性结直肠癌不同治疗方案中的疗效和毒性

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摘要

The aim of the present study was to describe treatment outcomes for bevacizumab in combination with chemotherapy based on data from the Czech registry of targeted therapies for metastatic colorectal cancer (mCRC). Patients and Methods: In total, 4,487 patients with mCRC who received bevacizumab combined with chemotherapy in first line (n=3,990, 88.9%), second line (n=386, 8.6%), or third/higher line (n=lll, 2.5%) had evaluable data and were included in the present retrospective analysis. Results: The median progression-free survival (PFS) was 11.3 months (95% conficence interval [CI]=11.0-11.7 months), 9.5 months (95% CI=8.2-10.9 months), and 7.3 months (95% CI=5.9-8.7 months; p<0.001), and the median overall survival from the start of bevacizumab-containing therapy was 28.4 months (95% CI=27.1-29.8 months), 25.9 months (95% CI=19.4~ 32.4 months), and 15.0 months (95% CI=10.7-19.3 months; p<0.001), respectively. Conclusion: The data describe efficacy of bevacizumab with chemotherapy for different treatment lines in a large patient cohort.
机译:本研究的目的是根据捷克针对转移性结直肠癌(mCRC)的靶向治疗注册数据,描述贝伐单抗联合化疗的治疗结果。患者和方法:一线(n = 3,990,88.9%),二线(n = 386、8.6%)或三线/更高线(n = III)接受贝伐单抗联合化疗的4,487例mCRC患者2.5%)具有可评估的数据,并已包括在本回顾性分析中。结果:中位无进展生存期(PFS)为11.3个月(95%置信区间[CI] = 11.0-11.7个月),9.5个月(95%CI = 8.2-10.9个月)和7.3个月(95%CI = 5.9-8.7个月; p <0.001),从开始使用贝伐单抗开始的中位总生存期为28.4个月(95%CI = 27.1-29.8个月),25.9个月(95%CI = 19.4〜32.4个月),和15.0个月(95%CI = 10.7-19.3个月; p <0.001)。结论:这些数据描述了贝伐单抗联合化疗对大患者队列不同治疗方案的疗效。

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