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用于治疗淋巴系统恶性肿瘤的双特异性抗体。

Bispecific Antibodies for Lymphoid Malignancy Treatment.

作者信息

Bisio Matteo, Legato Luca, Fasano Filippo, Benevolo Savelli Corrado, Boccomini Carola, Nicolosi Maura, Santambrogio Elisa, Freilone Roberto, Novo Mattia, Botto Barbara

机构信息

Hematology Division, A.O.U. Città della Salute e della Scienza di Torino, C.so Bramante 88, 10126 Turin, Italy.

出版信息

Cancers (Basel). 2024 Dec 31;17(1):94. doi: 10.3390/cancers17010094.

Abstract

BACKGROUD

The introduction of highly active immunotherapies has changed the outcome of B-cell non-Hodgkin lymphomas (B-NHLs) in the last two decades. Since then, important progress has been shown using newer and more active immunotherapies, including chimeric antigen receptor T-cell therapy (CAR-T), conjugated monoclonal antibodies, and bispecific antobodies, which currently plays a significant role in the treatment of diffuse large B-cell (DLBCL), follicular (FL), and mantle cell (MCL) lymphoma.

PURPOSE

In this review, we provide an updated overview of recently completed and ongoing BsAb trials in patients with relapsed/refractory(R/R) B-NHL and Hodgkin's lymphoma, including single-agent results, emerging combinations, safety data, and novel constructs.

CONCLUSIONS

Bispecific antibodies (BsAbs) are a novel class of "off-the-shelf" T-cell-redirecting drugs capable of targeting various cell-surface antigens. New antigen targets are currently under investigation, such as CD19 × CD3 and CD30 × CD3 or CD30 × CD16, in different settings. BsAbs are among the most promising therapeutic options for lymphoma today since they have demonstrated significant single-agent activity, along with a manageable toxicity profile, in patients with heavily pretreated B-NHL.

摘要

背景

在过去二十年中,高活性免疫疗法的引入改变了B细胞非霍奇金淋巴瘤(B-NHL)的治疗结果。从那时起,使用更新、更有效的免疫疗法取得了重要进展,包括嵌合抗原受体T细胞疗法(CAR-T)、偶联单克隆抗体和双特异性抗体,这些疗法目前在弥漫性大B细胞淋巴瘤(DLBCL)、滤泡性淋巴瘤(FL)和套细胞淋巴瘤(MCL)的治疗中发挥着重要作用。

目的

在本综述中,我们提供了关于复发/难治性(R/R)B-NHL和霍奇金淋巴瘤患者近期完成和正在进行的双特异性抗体(BsAb)试验的最新概述,包括单药治疗结果、新出现的联合治疗、安全性数据和新型构建体。

结论

双特异性抗体(BsAbs)是一类新型的“现成可用”的T细胞重定向药物,能够靶向多种细胞表面抗原。目前正在不同背景下研究新的抗原靶点,如CD19×CD3、CD30×CD3或CD30×CD16。双特异性抗体是当今淋巴瘤最有前景的治疗选择之一,因为它们在经过大量预处理的B-NHL患者中已显示出显著的单药活性以及可控的毒性特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3037/11719988/74de62a5dd64/cancers-17-00094-g001.jpg

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