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

IF 4.9 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Darren Pan, Anupama Kumar, Jodi J Lipof, Alfred Chung, Jeffrey L Wolf, Thomas G Martin, Shagun Arora, Peter H Sayre, Ajai Chari
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引用次数: 0

Abstract

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.

新兴的gprc5d靶向治疗多发性骨髓瘤:全面回顾。
GPRC5D是一种很有前景的骨髓瘤相关抗原,目前正在积极研究几种GPRC5D靶向治疗方法,包括CAR - T细胞、双特异性和三特异性抗体以及抗体-药物偶联物。这类药物有望改变多发性骨髓瘤治疗的格局。涵盖的领域:在这里,我们回顾了GPRC5D的生物学,目前和新出现的talquetamab在复发/难治性多发性骨髓瘤中的应用,研究GPRC5D靶向药物的前景,以及这些药物如何可能在未来的临床实践中实施。专家意见:Talquetamab是目前唯一被批准的GPRC5D靶向治疗药物,主要用于BCMA难治性多发性骨髓瘤,但没有生物学原因表明BCMA治疗必须用尽才能靶向GPRC5D;以创新的方式利用GPRC5D将是充分发挥其治疗潜力的关键。较新的试验正在探索更积极的方法,将多个免疫治疗靶点结合在一条线上,以防止耐药性,并有可能实现治愈。虽然gprc5d靶向治疗非常有效,但它们也存在显著的毒性风险,包括口腔、皮肤、指甲和小脑毒性。除了提高疗效,未来的研究还必须集中在优化剂量,识别毒性生物标志物,制定更好的策略来管理不良事件,以优化这些疗法的风险-收益概况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.00
自引率
0.00%
发文量
71
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Investigational Drugs (ISSN 1354-3784 [print], 1744-7658 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles and original papers on drugs in preclinical and early stage clinical development, providing expert opinion on the scope for future development. The Editors welcome: Reviews covering preclinical through to Phase II data on drugs or drug classes for specific indications, and their potential impact on future treatment strategies Drug Evaluations reviewing the clinical and pharmacological data on a particular drug Original Research papers reporting the results of clinical investigations on agents that are in Phase I and II clinical trials The audience consists of scientists, managers and decision-makers in the pharmaceutical industry, and others closely involved in R&D.
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