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Efficacy of sequential therapies with sorafenib-sunitinib versus sunitinib-sorafenib in metastatic renal cell carcinoma: A systematic review and meta-analysis

机译:索拉非尼-舒尼替尼与舒尼替尼-索拉非尼序贯疗法在转移性肾细胞癌中的疗效:系统评价和荟萃分析

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摘要

The most efficient sequence of targeted agents for metastatic renal cell carcinoma patients has yet to be identified. Whether the sequence of sorafenib and sunitinib really matters is controversial and not answered clearly until now. This meta-analysis aims to estimate the efficacy of receptor tyrosine kinase inhibitors sorafenib-sunitinib and sunitinib-sorafenib for metastatic renal cell carcinoma, on the outcome of first-line progression-free survival, second-line progression-free survival, total progression-free survival and overall survival.We searched PubMed, Embase, Cochrane Library and for eligible studies. Data were analyzed using random or fixed effects model depending on the heterogeneity of the eligible studies. Heterogeneity across studies were analyzed using Q and I2 statistics.Of 902 identified studies, ten were qualified in our analysis (N = 1732 patients). Sorafenib-sunitinib yielded no statistically significant benefit in first-line progression-free survival (fixed effects; HR = 0.95; 95%CI 0.75-1.21; p = 0.702), total progression-free survival (random effects; HR = 0.92; 95%CI 0.71-1.19; p = 0.531) and overall survival (fixed effects; HR = 0.89; 95%CI 0.72-1.09; p = 0.257), compared with sunitinib-sorafenib. Second-line progression-free survival was longer for sorafenib-sunitinib than sunitinib-sorafenib (fixed effects; HR = 0.55; 95%CI 0.44-0.68; p = 0.000).Sequential therapies with sorafenib and sunitinib is well tolerated and efficient in mRCC. However, there are no evidence supported that sorafenib–sunitinib has the superiority to sunitinib-sorafenib in sequence. The ideal sequence of targeted agents requires further elucidation.
机译:对于转移性肾细胞癌患者,最有效的靶向药物序列尚未确定。索拉非尼和舒尼替尼的序列是否真的很重要,目前尚无定论。这项荟萃分析旨在评估受体酪氨酸激酶抑制剂索拉非尼-舒尼替尼和舒尼替尼-索拉非尼在转移性肾细胞癌中的疗效,涉及一线无进展生存期,二线无进展生存期,总进展期-免费生存率和总体生存率。我们在PubMed,Embase,Cochrane库和相关研究中进行了搜索。根据合格研究的异质性,使用随机或固定效应模型分析数据。使用Q和I2统计数据分析了研究的异质性。在902项已鉴定的研究中,有10项在我们的分析中合格(N = 1732例患者)。索拉非尼-舒尼替尼对一线无进展生存期(固定效应; HR = 0.95; 95%CI 0.75-1.21; p = 0.702),总无进展生存期(随机效应; HR = 0.92; 95)没有统计学意义的获益与舒尼替尼-索拉非尼相比,%CI 0.71-1.19; p = 0.531)和总生存期(固定效应; HR = 0.89; 95%CI 0.72-1.09; p = 0.257)。索拉非尼-舒尼替尼的二线无进展生存期比舒尼替尼-索拉非尼更长(固定效应; HR = 0.55; 95%CI 0.44-0.68; p = 0.000)。索拉非尼和舒尼替尼的序贯治疗在mRCC中耐受性良好且有效。然而,没有证据支持索拉非尼-舒尼替尼依序优于舒尼替尼-索拉非尼。靶向药物的理想序列需要进一步阐明。

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