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依鲁替尼单药或联合治疗复发/难治性弥漫大 B 细胞淋巴瘤(R/R DLBCL)的疗效与安全性:一项系统评价和 Meta 分析

英文原题:Efficacy and Safety of Ibrutinib as Monotherapy or Combination Therapy in Relapsed/Refractory Diffuse Large B-cell Lymphoma (R/R DLBCL): A Systematic Review and Meta-analysis.

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Efficacy and Safety of Ibrutinib as Monotherapy or Combination Therapy in Relapsed/Refractory Diffuse Large B-cell Lymphoma (R/R DLBCL): A Systematic Review and Meta-analysis.

PubMed 2024/10/16(内容时间) Am J Ther Q2 · IF 3.5(JCR 2025)

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研究概要

伊布替尼单药或联合治疗在治疗 R/R DLBCL 中安全有效,不良反应可耐受。

研究思路结论见上方概要

弥漫大B细胞淋巴瘤(DLBCL)是一种高度异质性的疾病群体。伊布替尼单药或联合治疗在复发/难治性(R/R)DLBCL中有效。然而,不同方案治疗R/R DLBCL的缓解率从15%到90%不等,耐受性仍存在争议。不确定领域:伊布替尼单药或联合治疗在R/R DLBCL患者中的疗效和安全性仍不确定。

检索了PubMed、CBM、MEDLINE、Cochrane Library和Embase数据库,检索时间从建库至2021年7月。治疗进展:接受ibrutinib治疗的R/R DLBCL患者的总完全缓解率(CRR)和总缓解率分别为26%和49%。ibrutinib联合治疗的CRR显著高于ibrutinib单药治疗(45% vs. 19%)。此外,双表达淋巴瘤患者的CRR为40%,中枢神经系统淋巴瘤为35%,非生发中心B细胞样(non-GCB)DLBCL为33%,均高于GCB亚型的8%。汇总的中位PFS和总生存期分别为5.57个月和10.17个月。GCB-DLBCL的总生存期最差(5.1个月)。然而,我们发现联合方案与单药治疗相比并无生存优势(P > 0.05),表明联合治疗仅是过渡性治疗以及CAR-T 细胞或其他治疗的桥接。此外,接受ibrutinib联合治疗的患者中有12%发生≥3级不良事件,而ibrutinib单药治疗为9%。

展开英文摘要原文

Diffuse large B-cell lymphoma (DLBCL) is a highly heterogeneous disease group. Ibrutinib's monotherapy or combination therapy is effective in relapsed/refractory (R/R) DLBCL. However, the treatment response in R/R DLBCL varies from 15% to 90% with different regimens, and the tolerance remains controversial. AREAS OF UNCERTAINTY: The efficacy and safety of ibrutinib monotherapy or combination therapy in patients with R/R DLBCL remain uncertain. DATA SOURCES: The PubMed, CBM, MEDLINE, Cochrane Library, and Embase databases were searched from their inception to July 2021. THERAPEUTIC ADVANCES: The total complete remission rate (CRR) and overall response rate in R/R DLBCL patients treated with ibrutinib were 26% and 49%, respectively. The CRR of ibrutinib combination therapy was significantly higher than the ibrutinib monotherapy (45% vs. 19%). Moreover, the CRR of patients was 40% in double expressing lymphoma, 35% in central nervous system lymphoma, and 33% in nongerminal center B-cell-like (non-GCB) DLBCL, which was higher than the 8% in those with the GCB subtype. The pooled median PFS and overall survival were 5.57 and 10.17 months, respectively. GCB-DLBCL had the worst overall survival (5.1 months). Nevertheless, we found that combination regimens had no survival advantage compared with monotherapy ( P > 0.05), indicating that combination therapy was only a transitional treatment and bridge for chimeric antigen receptor T cells or other treatments. Moreover, 12% of patients on ibrutinib combination therapy had ≥grade 3 adverse events compared with 9% on ibrutinib monotherapy.

Ibrutinib monotherapy or combination therapy was safe and effective in treating R/R DLBCL with tolerable adverse reactions.

论文信息

作者
Li Y、Li C、Lv K、Wang S、Li F
单位
Jiangxi Provincial Key Laboratory of Hematological Diseases, Department of Hematology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China; and.China
文献类型
系统综述 · 荟萃分析
期刊
American journal of therapeutics2025 Jan-Feb 01
原文标识
PubMed 39413356 · DOI 10.1097/MJT.0000000000001831