University of California San Francisco, San Francisco, CA, USA.
Mount Sinai Hospital, New York, NY, USA.
Leukemia. 2020 Apr;34(4):985-1005. doi: 10.1038/s41375-020-0734-z. Epub 2020 Feb 13.
Despite considerable advances in the treatment of multiple myeloma (MM) in the last decade, a substantial proportion of patients do not respond to current therapies or have a short duration of response. Furthermore, these treatments can have notable morbidity and are not uniformly tolerated in all patients. As there is no cure for MM, patients eventually become resistant to therapies, leading to development of relapsed/refractory MM. Therefore, an unmet need exists for MM treatments with novel mechanisms of action that can provide durable responses, evade resistance to prior therapies, and/or are better tolerated. B-cell maturation antigen (BCMA) is preferentially expressed by mature B lymphocytes, and its overexpression and activation are associated with MM in preclinical models and humans, supporting its potential utility as a therapeutic target for MM. Moreover, the use of BCMA as a biomarker for MM is supported by its prognostic value, correlation with clinical status, and its ability to be used in traditionally difficult-to-monitor patient populations. Here, we review three common treatment modalities used to target BCMA in the treatment of MM: bispecific antibody constructs, antibody-drug conjugates, and chimeric antigen receptor (CAR)-modified T-cell therapy. We provide an overview of preliminary clinical data from trials using these therapies, including the BiTE® (bispecific T-cell engager) immuno-oncology therapy AMG 420, the antibody-drug conjugate GSK2857916, and several CAR T-cell therapeutic agents including bb2121, NIH CAR-BCMA, and LCAR-B38M. Notable antimyeloma activity and high minimal residual disease negativity rates have been observed with several of these treatments. These clinical data outline the potential for BCMA-targeted therapies to improve the treatment landscape for MM. Importantly, clinical results to date suggest that these therapies may hold promise for deep and durable responses and support further investigation in earlier lines of treatment, including newly diagnosed MM.
尽管在过去十年中多发性骨髓瘤 (MM) 的治疗取得了相当大的进展,但相当一部分患者对当前的治疗方法没有反应或反应持续时间短。此外,这些治疗方法可能会带来显著的发病率,并且并非所有患者都能耐受。由于 MM 无法治愈,患者最终会对治疗产生耐药性,导致复发性/难治性 MM 的发展。因此,存在对具有新型作用机制的 MM 治疗方法的未满足需求,这些方法可以提供持久的反应、逃避对先前治疗的耐药性,并且/或者耐受性更好。B 细胞成熟抗原 (BCMA) 在成熟 B 淋巴细胞中优先表达,其过度表达和激活与临床前模型和人类的 MM 相关,支持其作为 MM 治疗靶点的潜在用途。此外,BCMA 作为 MM 的生物标志物,其具有预后价值、与临床状态的相关性,并且能够用于传统上难以监测的患者群体,这也支持了其在 MM 中的应用。在此,我们综述了用于 MM 治疗中靶向 BCMA 的三种常见治疗方式:双特异性抗体构建体、抗体药物偶联物和嵌合抗原受体 (CAR) 修饰的 T 细胞疗法。我们提供了使用这些疗法的临床试验的初步临床数据概述,包括 BiTE®(双特异性 T 细胞衔接器)免疫肿瘤学疗法 AMG 420、抗体药物偶联物 GSK2857916 和几种 CAR T 细胞治疗剂,包括 bb2121、NIH CAR-BCMA 和 LCAR-B38M。这些治疗方法中的几种方法已经观察到显著的抗骨髓瘤活性和高微小残留病阴性率。这些临床数据概述了 BCMA 靶向治疗改善 MM 治疗前景的潜力。重要的是,迄今为止的临床结果表明,这些疗法可能具有深度和持久反应的潜力,并支持在包括新诊断 MM 在内的更早治疗线中进一步研究。