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Efficacy and safety of B-cell receptor signaling pathway inhibitors in relapsed/refractory chronic lymphocytic leukemia: a systematic review and meta-analysis of randomized clinical trials

机译:B细胞受体信号传导途径抑制剂在复发/难治性慢性淋巴细胞白血病中的功效和安全性:随机临床试验的系统评价和荟萃分析

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ABSTRACT Ibrutinib and idelalisib, B-cell receptor (BCR) signaling pathway inhibitors, have been recently approved for use against relapsed/refractory chronic lymphocytic leukemia (CLL). To assess the efficacy and safety of BCR pathway inhibitors in relapsed/refractory CLL, we conducted a systematic review and meta-analysis of five randomized controlled trials (1866 patients). Our study demonstrated that BCR pathway inhibitors significantly prolonged progression-free survival (PFS; pooled HR = 0.24; 95% Cl: 0.19-0.30) and overall survival (HR = 0.58; 0.46-0.73) compared with control treatment. BCR pathway inhibitors increased the probability of response (RR = 3.54; 95% Cl: 1.69-7.41) and decreased the risk of progression (RR = 0.21, 95% Cl: 0.13-0.34). However, BCR pathway inhibitors increased the risk of grade 3 and 4 adverse events (AEs; RR=1.25; 95% Cl: 1.08-1.44) and serious AEs (RR = 1.32; 95% Cl: 1.17-1.50). AEs causing discontinuation (RR=1.26; 95% Cl: 0.88-1.81) or death (RR=1.06; 95% Cl: 0.72-1.57) were not significantly increased. No statistically significant difference in any aspect of meta-analysis was noted between ibrutinib and idelalisib.
机译:摘要最近批准了伊布洛替尼和伊德利赖米,B细胞受体(BCR)信号通路抑制剂,用于对复发/难治性慢性淋巴细胞白血病(CLL)使用。为了评估BCR途径抑制剂在复发/难治性CLL中的疗效和安全性,我们对五种随机对照试验进行了系统审查和荟萃分析(1866名患者)。我们的研究表明,BCR途径抑制剂显着延长了无进展的存活率(PFS;合并的HR = 0.24; 95%CL:0.19-0.30)和总存活(HR = 0.58; 0.46-0.73)与对照处理相比。 BCR途径抑制剂增加了响应的概率(RR = 3.54; 95%CL:1.69-7.41)并降低进展的风险(RR = 0.21,95%CL:0.13-0.34)。然而,BCR途径抑制剂增加了3级和4级不良事件(AES; RR = 1.25; 95%CL:1.08-1.44)和严重AES(RR = 1.32; 95%CL:1.17-1.50)的风险。 AES导致停止(RR = 1.26; 95%CL:0.88-1.81)或死亡(RR = 1.06; 95%CL:0.72-1.57)没有显着增加。在Ibrutinib和Idelalisib之间发现了Meta分析的任何方面的统计学意义。

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