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多发性骨髓瘤的新兴 GPRC5D 靶向治疗:综合综述

英文原题:Emerging GPRC5D-Targeted therapies for multiple myeloma: a comprehensive review.

查看英文原题

Emerging GPRC5D-Targeted therapies for multiple myeloma: a comprehensive review.

PubMed 2025/05/28(内容时间) Expert Opin Investig Drugs Q2 · IF 4.3(JCR 2025)

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研究概要

Talquetamab 是目前唯一获批的 GPRC5D 靶向治疗药物,主要用于 BCMA 难治性多发性骨髓瘤,但并没有生物学上的理由要求在靶向 GPRC5D 之前必须用尽 BCMA 治疗;

中文摘要

引言:GPRC5D是一种有前景的骨髓瘤相关抗原,多种靶向GPRC5D的疗法正在积极研究中,包括CAR-T 细胞、双特异性和三特异性抗体及抗体药物偶联物。这类药物有望改变多发性骨髓瘤的治疗格局。综述范围:本文综述GPRC5D生物学、塔奎妥单抗当前及新兴的复发/难治性多发性骨髓瘤临床应用、在研GPRC5D靶向药物现状,以及这些药物未来可能如何纳入临床实践。专家观点:目前塔奎妥单抗是唯一获批的GPRC5D靶向疗法,主要用于BCMA耐药性多发性骨髓瘤;但从生物学角度看,靶向GPRC5D前并无必须先用尽BCMA疗法的理由。创新性地利用GPRC5D对于充分发挥其治疗潜力至关重要。新近试验正探索在同一治疗线中更积极地联合多个免疫治疗靶点,以预防耐药并可能实现治愈。GPRC5D靶向疗法疗效显著,但也存在口腔、皮肤、指甲和小脑毒性等重大风险。未来研究除提高疗效外,还必须优化剂量、识别毒性生物标志物,并开发更佳不良事件管理策略,以优化这些疗法的获益–风险特征。

展开英文摘要原文

INTRODUCTION: GPRC5D is a promising myeloma-associated antigen, and several GPRC5D-targeted therapies are under active investigation, including CAR T cells, bispecific and trispecific antibodies, and antibody-drug conjugates. This class of agents is poised to transform the landscape of multiple myeloma treatment. AREAS COVERED: Here, we review the biology of GPRC5D, the current and emerging uses of talquetamab in relapsed/refractory multiple myeloma, the landscape of investigational GPRC5D-targeted drugs, and how these agents are likely to be implemented into future clinical practice.

EXPERT OPINION: Talquetamab is currently the only approved GPRC5D-targeted therapy, primarily used for BCMA-refractory multiple myeloma, but there is no biological reason BCMA therapies must be exhausted before targeting GPRC5D; utilizing GPRC5D in innovative ways will be key to fully realizing its therapeutic potential.

Newer trials are exploring more aggressive approaches combining multiple immunotherapy targets within a single line to prevent resistance and potentially achieve a cure. While GPRC5D-targeted therapies are highly effective, they also pose significant toxicity risks including oral, skin, nail, and cerebellar toxicity.

In addition to improving efficacy, future research must also focus on optimizing dosing, identifying biomarkers for toxicity, and developing better strategies for managing adverse events to optimize the risk-benefit profile of these therapies.

论文信息

作者
Pan D、Kumar A、Lipof JJ、Chung A、Wolf JL、Martin TG 3rd、Arora S、Sayre PH
单位
Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.United States
文献类型
综述
期刊
Expert opinion on investigational drugs2025 May
原文标识
PubMed 40425184 · DOI 10.1080/13543784.2025.2511179