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嵌合抗原受体 T 细胞在多发性骨髓瘤中的未来。

Future of CAR T cells in multiple myeloma.

机构信息

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Research Unit in Translational Hematology, Department of Medicine, Chulalongkorn University, Bangkok, Thailand.

出版信息

Hematology Am Soc Hematol Educ Program. 2020 Dec 4;2020(1):272-279. doi: 10.1182/hematology.2020000111.

Abstract

Despite the significant improvement in survival outcomes of multiple myeloma (MM) over the past decade, it remains an incurable disease. Patients with triple-class refractory MM have limited treatment options and a dismal prognosis. Chimeric antigen receptor (CAR) T-cell therapy targeting B-cell maturation antigen has transformed the treatment armamentarium of relapsed/refractory MM (RRMM), with unprecedented overall response rates in this difficult-to-treat patient population. However, a significant proportion of patients ultimately relapse despite achieving deep remission. Several innovative approaches, including alternative/dual-antigen-specific CAR T-cell constructs, genetically engineered "off-the-shelf" CAR T cells, and strategies to counteract an immunosuppressive microenvironment, may dramatically reshape the field of CAR T-cell therapy in the future. These strategies are being actively investigated in preclinical and early clinical trial settings with the hopes of enhancing the durability of responses and, thereby, improving the overall survival of RRMM patients after CAR T-cell therapy.

摘要

尽管过去十年多发性骨髓瘤(MM)的生存结果有了显著改善,但它仍然是一种无法治愈的疾病。三药难治性 MM 患者的治疗选择有限,预后不良。针对 B 细胞成熟抗原的嵌合抗原受体(CAR)T 细胞疗法改变了复发/难治性 MM(RRMM)的治疗手段,在这一治疗困难的患者群体中达到了前所未有的总缓解率。然而,尽管达到了深度缓解,仍有相当一部分患者最终复发。一些创新方法,包括替代/双抗原特异性 CAR T 细胞构建体、基因工程“现成”CAR T 细胞,以及对抗免疫抑制微环境的策略,可能会在未来极大地改变 CAR T 细胞治疗领域。这些策略正在临床前和早期临床试验中进行积极研究,以期提高缓解的持久性,从而改善 RRMM 患者在接受 CAR T 细胞治疗后的总体生存率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59b6/7727578/a88800ad54a4/bloodbook-2020-272-absf1.jpg

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Anti-BCMA chimeric antigen receptors with fully human heavy-chain-only antigen recognition domains.
Nat Commun. 2020 Jan 15;11(1):283. doi: 10.1038/s41467-019-14119-9.
5
CAR-NK for tumor immunotherapy: Clinical transformation and future prospects.
Cancer Lett. 2020 Mar 1;472:175-180. doi: 10.1016/j.canlet.2019.11.033. Epub 2019 Nov 29.
6
T-cell phenotypes associated with effective CAR T-cell therapy in postinduction vs relapsed multiple myeloma.
Blood Adv. 2019 Oct 8;3(19):2812-2815. doi: 10.1182/bloodadvances.2019000600.
8
Anti-B-cell Maturation Antigen Chimeric Antigen Receptor T cell Function against Multiple Myeloma Is Enhanced in the Presence of Lenalidomide.
Mol Cancer Ther. 2019 Dec;18(12):2246-2257. doi: 10.1158/1535-7163.MCT-18-1146. Epub 2019 Aug 8.
9
Chimeric Antigen Receptor-Modified T Cell Therapy in Multiple Myeloma: Beyond B Cell Maturation Antigen.
Front Immunol. 2019 Jul 16;10:1613. doi: 10.3389/fimmu.2019.01613. eCollection 2019.

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