CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
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.
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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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。
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%。
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.
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