Kim Jinchul, Cho Jinhyun, Lim Joo Han, Lee Moon Hee
Department of Hematology-Oncology, Inha University College of Medicine and Hospital, 7-206 Third Street, Shinheung-Dong Jung-Gu, Incheon, Republic of Korea.
Blood Res. 2025 Jan 2;60(1):1. doi: 10.1007/s44313-024-00038-2.
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.
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.
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%.
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.
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。
我们进行了一项系统的文献综述,以识别使用PubMed、EMBASE、Cochrane数据库以及截至2023年12月发表的会议摘要中所有公开可用的随机对照试验(RCT)。进行了贝叶斯网络荟萃分析,以估计无进展生存期(PFS)的风险比(HRs)及其95%置信区间(CIs),并确定纳入方案的排名。
荟萃分析纳入了12项试验,涉及4437例患者和13种治疗方案。维奈克拉联合利妥昔单抗和泽布替尼成为R/R CLL总体人群中最有效的治疗方法,与伊布替尼相比,其PFS HR最低(分别为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(累积排名曲线下面积[SUCRA]值分别为90%)。在17p缺失/TP53突变亚组中,泽布替尼显示出最有利的疗效(与伊布替尼相比,HR 0.52,95%CI 0.31 - 0.88),SUCRA值最高(97%)。在没有这些突变的患者中,维奈克拉联合利妥昔单抗最有效(与伊布替尼相比,HR 0.49,95%CI 0.26 - 0.94),SUCRA值为94%。
我们的研究结果突出了维奈克拉联合利妥昔单抗和泽布替尼治疗R/R CLL的卓越疗效,并证实每种方案的作用可能因具有临床意义的突变而异。