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CAR-T 细胞治疗后复发/难治性大 B 细胞淋巴瘤:当前挑战与治疗选择

英文原题:Relapsed or refractory large B-cell lymphoma after chimeric antigen receptor T-cell therapy: Current challenges and therapeutic options.

查看英文原题

Relapsed or refractory large B-cell lymphoma after chimeric antigen receptor T-cell therapy: Current challenges and therapeutic options.

PubMed 2023/01/29(内容时间) Br J Haematol Q2 · IF 3.6(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

嵌合抗原受体(CAR)T细胞疗法可使化学免疫治疗失败后的复发/难治性弥漫大B细胞淋巴瘤(DLBCL)患者获得持久缓解。然而,CAR-T 治疗后仍难治或复发的患者结局较差。研究者已提出多种CAR-T 治疗失败机制,但这类患者的管理仍具挑战。随着CAR-T 治疗逐步前移至DLBCL治疗早期,亟需专门针对CAR-T 治疗后复发患者开展临床试验。双特异性抗体、抗体药物偶联物和下一代CAR-T 疗法等新型免疫疗法近期取得进展,可能为治疗提供新途径。本文综述CAR-T 治疗失败后应用这些药物的现有数据,并提出合理排序使用这些新型药物的框架。

展开英文摘要原文

Chimeric antigen receptor (CAR) T-cell (CAR-T) therapy can provide durable remission in patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) after failure of chemoimmunotherapy.

However, patients who are refractory or relapsing after CAR-T therapy have poor outcomes. Multiple mechanisms of CAR-T therapy failure have been proposed but management of these patients remains a challenge. As CAR-T therapy moves earlier in the treatment of DLBCL, we urgently need trials focused on patients with relapse after CAR-T therapy. Recent advances in novel immunotherapies such as bispecific antibodies, antibody-drug conjugates and next-generation CAR-T therapies may provide avenues for treatment.

Here we review the available data on using these drugs after failure of CAR-T therapy and provide a framework for the ideal sequencing of these novel agents.

论文信息

作者
Del Toro-Mijares R、Oluwole O、Jayani RV、Kassim AA、Savani BN、Dholaria B
第一作者单位
Escuela de Medicina, Tecnologico de Monterrey, Monterrey, Mexico.Mexico
通讯作者单位
Department of Hematology-Oncology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.United States
文献类型
综述
期刊
British journal of haematology2023 Apr
原文标识
PubMed 36709623 · DOI 10.1111/bjh.18656