首页> 外文期刊>Journal of the Formosan Medical Association =: Taiwan yi zhi >Real-world evidence of the safety and effectiveness of regorafenib in Taiwanese patients with metastatic colorectal cancer: CORRELATE Taiwan
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Real-world evidence of the safety and effectiveness of regorafenib in Taiwanese patients with metastatic colorectal cancer: CORRELATE Taiwan

机译:现实世界探讨了台湾转移性结直肠癌患者中雷龙嫩的安全和有效性:台湾相关

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Background/PurposeThis analysis reports safety and effectiveness data from the Taiwanese cohort of the CORRELATE study.MethodsCORRELATE was a prospective, observational study to assess the safety and effectiveness of regorafenib for the treatment of metastatic colorectal cancer (CRC) in real-world clinical practice that was conducted in 13 different countries in Asia, Europe and Latin America. The primary endpoint of the study was incidence of all treatment-emergent AEs (TEAEs), and secondary endpoints included overall survival (OS), progression-free survival (PFS), and disease control rate (DCR).ResultsThe global study population (N?=?1037) included 128 Taiwanese patients with a median age of 64 years, median weight of 62.02?kg and 66.41% were male. Reduced initiating doses of regorafenib and dose interruptions were common in Taiwanese patients (71.87% and 50.00%, respectively). The safety profile of regorafenib was consistent with that seen in Asian patients in the clinical development trials, including the CORRECT and CONCUR studies, with hand–foot–skin reactions (HFSR) of any grade occurring in 33.59% of patients. Median OS was 11.64 months in the Taiwanese patients (95% confidence interval [CI], 8.36–13.82) and median PFS was 2.17 months (95% CI, 1.97–2.89).ConclusionThe safety and effectiveness of regorafenib in this real-world study was generally consistent with the known efficacy and safety profile in Asian patients in clinical trials.Trial registrationNCT02042144.
机译:背景/ putposethis分析报告了与相关研究的台湾队列的安全和有效性数据。方法是评估Regorafenib在现实世界临床实践中治疗转移性结肠直肠癌(CRC)的安全性和有效性的前瞻性的观察性研究是在亚洲,欧洲和拉丁美洲的13个不同国家进行的。该研究的主要终点是所有治疗新的AES(茶)的发病率,次级终点包括整体存活(OS),无进展的存活(PFS)和疾病控制率(DCR).Resultsthe全球研究人群(n ?= 1037)包括64岁的台湾患者128名患者,中位重62.02克,66.41%是男性。降低的起始剂量的雄育和剂量中断在台湾患者中常见(分别为71.87%和50.00%)。 Regorafenib的安全性曲线与临床开发试验中的亚洲患者中观察到的,包括正确和同意的研究,在33.59%的患者中发生任何等级的手动脚皮肤反应(HFSR)。台湾患者中位数OS是11.64个月(95%置信区间[CI],8.36-13.82)和中位数PFS为2.17个月(95%CI,1.97-2.89)。结论真实研究中霍龙赛的安全性和有效性通常与临床试验中的亚洲患者中已知的疗效和安全性曲线一致.TRIAL REGICALIALNCT02042144。

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