Relative efficacy of systemic treatments for patients with relapsed/refractory chronic lymphocytic leukemia: a network meta-analysis according to 17p deletion/TP53 mutations.

IF 2.3 Q2 HEMATOLOGY
Jinchul Kim, Jinhyun Cho, Joo Han Lim, Moon Hee Lee
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引用次数: 0

Abstract

Purpose: This network meta-analysis aimed to evaluate the relative efficacy of systemic treatments in patients with relapsed/refractory chronic lymphocytic leukemia (R/R CLL), focusing on key genetic mutations, specifically the 17p deletion and TP53 mutations.

Methods: We conducted a systematic literature review to identify all publicly available randomized controlled trials (RCTs) using PubMed, EMBASE, the Cochrane database, and meeting abstracts published through December 2023. A Bayesian network meta-analysis was performed to estimate the hazard ratios (HRs) for progression-free survival (PFS) with 95% confidence intervals (CIs) and to determine the ranking of the included regimens.

Results: Twelve trials involving 4,437 patients and 13 treatment options were included in the meta-analysis. Venetoclax plus rituximab and zanubrutinib emerged as the most effective treatments for the overall R/R CLL population, showing the lowest PFS HR (HR 0.62, 95% CI 0.32-1.20 and HR 0.65, 95% CI 0.49-0.86, respectively) versus ibrutinib, and were ranked as the best agent (surface under the cumulative ranking curve [SUCRA] value of both 90%, respectively) among the included drugs. In the 17p deletion/TP53 mutation subgroup, zanubrutinib demonstrated the most favorable efficacy (HR 0.52, 95% CI 0.31-0.88 versus ibrutinib) with the highest SUCRA value (97%). In patients without these mutations, venetoclax plus rituximab was the most effective (HR 0.49, 95% CI 0.26-0.94 versus ibrutinib) with a SUCRA value of 94%.

Conclusion: Our findings highlight the superior efficacy of venetoclax plus rituximab and zanubrutinib for treating R/R CLL and confirm that the role of each regimen may vary depending on the clinically significant mutations.

复发/难治性慢性淋巴细胞白血病患者全身治疗的相对疗效:基于17p缺失/TP53突变的网络meta分析
目的:本网络荟萃分析旨在评估复发/难治性慢性淋巴细胞白血病(R/R CLL)患者全身治疗的相对疗效,重点关注关键基因突变,特别是17p缺失和TP53突变。方法:我们进行了系统的文献综述,使用PubMed、EMBASE、Cochrane数据库和截至2023年12月发表的会议摘要,确定所有公开可用的随机对照试验(rct)。采用贝叶斯网络进行meta分析,以95%置信区间估计无进展生存期(PFS)的风险比(hr),并确定纳入方案的排名。结果:meta分析纳入了12项试验,涉及4,437例患者和13种治疗方案。Venetoclax + rituximab和zanubrutinib是总体R/R CLL人群最有效的治疗方法,与ibrutinib相比,PFS HR最低(HR 0.62, 95% CI 0.32-1.20和HR 0.65, 95% CI 0.49-0.86),并且在纳入的药物中被评为最佳药物(在累积排名曲线下的表面[SUCRA]值分别为90%)。在17p缺失/TP53突变亚组中,扎鲁替尼表现出最有利的疗效(HR 0.52, 95% CI 0.31-0.88 vs伊鲁替尼),SUCRA值最高(97%)。在没有这些突变的患者中,venetoclax + rituximab是最有效的(HR 0.49, 95% CI 0.26-0.94 vs ibrutinib), SUCRA值为94%。结论:我们的研究结果强调了venetoclax联合利妥昔单抗和zanubrutinib治疗R/R CLL的优越疗效,并证实了每种方案的作用可能因临床显著突变而异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Blood Research
Blood Research HEMATOLOGY-
CiteScore
3.70
自引率
0.00%
发文量
64
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