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弥漫大 B 细胞淋巴瘤中的 T 细胞衔接抗体——最新进展

英文原题:T-Cell Engaging Antibodies in Diffuse Large B Cell Lymphoma-An Update.

查看英文原题

T-Cell Engaging Antibodies in Diffuse Large B Cell Lymphoma-An Update.

PubMed 2023/10/25(内容时间) J Clin Med Q1 · IF 3.3(JCR 2025)

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中文摘要

新型细胞免疫疗法,如T细胞衔接抗体(TCEAbs),正在改变弥漫性大B细胞淋巴瘤(DLBCL)的治疗格局,尤其是在复发/难治性(R/R)情况下。TCEAbs通过同时结合肿瘤抗原和T细胞受体,利用宿主免疫系统的力量诱导肿瘤细胞杀伤。自blinatumomab获批用于R/R急性淋巴细胞白血病以来,新型TCEAbs取得了显著进展。许多此类新型TCEAbs在R/R DLBCL中显示出有前景的疗效,即使在经过大量预处理的患者中,也具有良好的缓解率,包括完全缓解。TCEAbs具有独特的治疗相关毒性,即细胞因子释放综合征(CRS)和免疫效应细胞相关神经毒性(ICANS),正确识别和管理这些副作用非常重要。本综述探讨了这些TCEAbs的发展和作用机制,以及临床试验中已发表的数据。还将讨论它们在DLBCL治疗中的作用、治疗相关不良事件的管理以及耐药机制。

展开英文摘要原文

Novel cellular immunotherapies such as T-cell engaging antibodies (TCEAbs) are changing the landscape of treatment for diffuse large B cell lymphoma (DLBCL), especially in the relapsed/refractory (R/R) setting. TCEAbs harness the power of the host immune system to induce killing of tumor cells by binding to both the tumor antigen and the T-cell receptor. Since the approval of blinatumomab for R/R acute lymphoblastic leukemia, there has been significant development in novel TCEAbs. Many of these novel TCEAbs have shown promising effectiveness in R/R DLBCL, with favorable response rates including complete remissions, even in heavily pretreated patients.

There are unique therapy-related toxicities with TCEAbs, namely cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity (ICANS), and it is important to both recognize and manage these side effects appropriately. This review examines the development and mechanism of action of these TCEAbs, and the available published data from clinical trials. Their role in the treatment of DLBCL, the management of therapy-related adverse events, and the mechanisms of resistance will also be discussed.

论文信息

作者
Balendran S、Tam C、Ku M
第一作者单位
Alfred Health, Melbourne, VIC 3004, Australia.Australia
通讯作者单位
St. Vincent's Hospital, Melbourne, Fitzroy, VIC 3065, Australia.Australia
文献类型
综述
期刊
Journal of clinical medicine2023 Oct 25
原文标识
PubMed 37959202 · DOI 10.3390/jcm12216737