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Safety and effectiveness of bevacizumab treatment for metastatic colorectal cancer: Final results from the Avastin? Registry - Investigation of Effectiveness and Safety (ARIES) observational cohort study

机译:贝伐单抗治疗转移性结直肠癌的安全性和有效性:Avastin的最终结果?注册表-有效性和安全性(ARIES)观察队列研究

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Aims: The Avastin? Registry - Investigation of Effectiveness and Safety (ARIES) observational cohort study (OCS) was designed to prospectively examine outcomes associated with bevacizumab-containing treatment for metastatic colorectal cancer (mCRC) in a community-based setting, where patient populations are less restricted than those in randomised trials. Materials and Methods: Patients with mCRC who were eligible for bevacizumab in combination with chemotherapy in first- or second-line treatment were enrolled from November 2006 to September 2008. There were no protocol-specified treatment regimens; the dose and schedule of bevacizumab and chemotherapy were at the treating physician's discretion. The objectives in the ARIES OCS included analyses of progression-free survival (PFS), overall survival, treatment patterns and safety in each of the first- and second-line treatment cohorts. Results: ARIES enrolled 1550 patients with mCRC receiving first-line therapy with bevacizumab. The median follow-up time was 20.6 months. The median PFS in this cohort was 10.2 months (95% confidence interval 9.8-10.6) and the median overall survival was 23.2 months (95% confidence interval 21.2-24.8). In a separate cohort of 482 patients with second-line mCRC, the median follow-up time was 16.9 months, the median PFS and overall survival from the start of second-line treatment to the end of follow-up was 7.9 months (95% confidence interval 7.2-8.3) and 17.8 months (95% confidence interval 16.5-20.7), respectively. Incidences of known bevacizumab-associated adverse events in ARIES were generally consistent with those previously reported in OCSs and randomised trials. Conclusion: Results from the prospective ARIES OCS add further evidence to support the effectiveness and safety of bevacizumab when added to first- and second-line treatment regimens for patients with mCRC in community treatment settings.
机译:目的:Avastin?注册表-有效性和安全性调查(ARIES)观察性队列研究(OCS)旨在前瞻性检查以社区为基础的患者人群受限制人群较少的,含贝伐单抗治疗转移性结直肠癌(mCRC)的相关结果在随机试验中。材料和方法:2006年11月至2008年9月,纳入一线或二线治疗中符合贝伐单抗联合化疗方案的mCRC患者。贝伐单抗和化疗的剂量和时间表由主治医师决定。 ARIES OCS的目标包括分析一线和二线治疗队列中的无进展生存期(PFS),总生存期,治疗模式和安全性。结果:ARIES招募了1550例接受贝伐单抗一线治疗的mCRC患者。中位随访时间为20.6个月。该队列的中位PFS为10.2个月(95%置信区间9.8-10.6),中位总体生存期为23.2个月(95%置信区间21.2-24.8)。在另一组482例二线mCRC患者中,中位随访时间为16.9个月,中位PFS和从二线治疗开始到随访结束的总生存期为7.9个月(95%)置信区间7.2-8.3)和17.8个月(95%置信区间16.5-20.7)。 ARIES中已知的贝伐单抗相关不良事件的发生率通常与先前在OCS和随机试验中报道的发生率一致。结论:前瞻性ARIES OCS的结果为在社区治疗环境中的mCRC患者的一线和二线治疗方案中添加贝伐单抗的有效性和安全性提供了进一步的证据。

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