化疗联合贝伐单抗治疗中国转移性结直肠癌患者的疗效和安全性:一项前瞻性、多中心、观察性、非介入性IV期试验

Fenghua Wang, Guanghai Dai, Yanhong Deng, Yong Tang, Wei Wang, Zuoxing Niu, Feng Bi, Liangjun Zhu, Zengqing Guo, Jin Yan, Bing Hu, Min Tao, Shujun Yang, Suzhan Zhang, Lu Wen, Ruihua Xu
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引用次数: 3

摘要

目的:贝伐单抗在改善全球转移性结直肠癌(mCRC)患者预后方面发挥着重要且不断发展的作用,并于2010年在中国获得批准。然而,关于化疗方案联合贝伐单抗治疗中国mCRC患者的有效性和安全性的实际数据有限。这项观察性的IV期试验研究旨在获得更多关于贝伐单抗联合化疗在中国mCRC患者中的有效性和安全性的经验。方法:2013年9月至2016年11月,在中国26个中心招募了组织学证实的mCRC患者参加了一项前瞻性、多中心、观察性、非介入性的IV期试验。符合条件的患者接受不同的化疗方案联合贝伐单抗。对意向治疗研究人群的疗效和安全性数据进行分析。结果:611例患者纳入疗效分析。中位总生存期和中位无进展生存期分别为18.00个月和10.05个月。客观有效率为21.00%,疾病控制率为89.40%。在亚组分析中,根据转移状态、治疗持续时间和血压升高观察生存差异。共有613名患者可进行安全性评估。569例(92.82%)患者报告了至少一次不良事件(AE), 151例(24.63%)患者报告了3级或以上不良事件。贝伐单抗相关不良事件的发生率在31例(5.06%)高血压(n=12)、脓肿和瘘管(n=7)、出血(n=6)、蛋白尿(n=3)、胃肠道穿孔(n=2)和静脉血栓形成事件(n=1)患者中报道。结论:这项观察性IV期试验拓宽了我们在中国人群中对贝伐单抗的经验和认识,并为其整体疗效和安全性提供了良好的指标。贝伐单抗联合化疗为中国mCRC患者提供了临床益处,并且具有可接受和可管理的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficacy and safety of chemotherapy combined with bevacizumab in Chinese patients with metastatic colorectal cancer: A prospective, multicenter, observational, non-interventional phase IV trial.

Efficacy and safety of chemotherapy combined with bevacizumab in Chinese patients with metastatic colorectal cancer: A prospective, multicenter, observational, non-interventional phase IV trial.

Efficacy and safety of chemotherapy combined with bevacizumab in Chinese patients with metastatic colorectal cancer: A prospective, multicenter, observational, non-interventional phase IV trial.

Objective: Bevacizumab has an important and evolving role in improving outcomes in patients with metastatic colorectal cancer (mCRC) worldwide and was approved in China in 2010. However, there are limited real-world data on the efficacy and safety of chemotherapy regimens combined with bevacizumab in Chinese patients with mCRC. This observational, phase IV trial study aimed to obtain more experience on the efficacy and safety of bevacizumab combined with chemotherapy in Chinese mCRC patients.

Methods: Between September 2013 and November 2016, patients with histologically confirmed mCRC were enrolled in a prospective, multicenter, observational, non-interventional phase IV trial at 26 centers across China. Eligible patients received different chemotherapeutic regimens combined with bevacizumab. The efficacy and safety data in the intention-to-treat study population were analyzed.

Results: A total of 611 patients were included in the efficacy analysis. The median overall survival and median progression-free survival was 18.00 and 10.05 months, respectively. The objective response rate was 21.00% and disease control rate was 89.40%. In subgroup analyses, the survival differences were observed according to metastatic status, duration of treatment and elevation in blood pressure. A total of 613 patients were evaluable for safety assessments. And 569 (92.82%) patients reported at least one adverse event (AE), and 151 (24.63%) experienced grade 3 or higher AEs. The incidence of bevacizumab-associated AEs of special interest was reported in 31 (5.06%) patients with hypertension (n=12), abscesses and fistulae (n=7), bleeding (n=6), proteinuria (n=3), gastrointestinal perforation (n=2) and venous thrombotic events (n=1).

Conclusions: This observational phase IV trial broadens our experience and knowledge of bevacizumab in the Chinese population and provides a good indication of its overall efficacy and safety. Bevacizumab in combination with chemotherapy offers clinical benefits to Chinese patients with mCRC and has an acceptable and manageable safety profile.

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