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多发性骨髓瘤中的抗体药物偶联疗法——未来有何新进展?

Antibody-drug conjugate therapies in multiple myeloma-what's next on the horizon?

作者信息

Hartley-Brown Monique, Richardson Paul

机构信息

Department of Medicine, Division of Medical Oncology, Harvard Medical School, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

出版信息

Explor Target Antitumor Ther. 2022;3(1):1-10. doi: 10.37349/etat.2022.00067. Epub 2022 Jan 14.

Abstract

Targeted immunotherapy has arisen over the past decade to the forefront of cancer care. Notably, targeted therapies such as antibody-drug conjugates (ADCs) are becoming more recognized for a novel approach in cancer treatment. The mechanism of action of ADCs incorporates a monoclonal antibody portion directed against the tumor cell antigen and attached to the tumoricidal portion via chemical linkage. The binding of the monoclonal antibody portion allows for tumor cell internalization of the ADC and precise release of the toxic payload within the cancer cell. Multiple myeloma (MM) is an incurable cancer for which belantamab mafodotin was the first-in-class ADC to achieve United States Food and Drug Administration (FDA) approval for treatment of this disease. Clinical trials are currently evaluating other ADCs in the treatment of MM. In this review, a look at the current ADCs being tested in MM clinical trials with a focus on those that are more promising and a potential next-in-line for FDA approval for treatment of MM is discussed.

摘要

在过去十年中,靶向免疫疗法已成为癌症治疗的前沿方法。值得注意的是,诸如抗体药物偶联物(ADC)等靶向疗法作为一种癌症治疗的新方法正越来越受到认可。ADC的作用机制包括一个针对肿瘤细胞抗原的单克隆抗体部分,该部分通过化学连接与杀肿瘤部分相连。单克隆抗体部分的结合使得ADC能够被肿瘤细胞内化,并在癌细胞内精确释放有毒载荷。多发性骨髓瘤(MM)是一种无法治愈的癌症,贝兰他单抗莫福汀是首个获得美国食品药品监督管理局(FDA)批准用于治疗该疾病的同类首创ADC。目前,临床试验正在评估其他ADC用于MM治疗的效果。在本综述中,将探讨目前正在MM临床试验中测试的ADC,重点关注那些更具前景且有可能成为下一个获得FDA批准用于MM治疗的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f90d/9400726/8721d6a5d4ea/etat-03-100267-g001.jpg

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