Stem Cell Transplantation and Cellular Therapies Unit (CTMO), Grande Ospedale Metropolitano "Bianchi-Melacrino-Morelli", Reggio Calabria, Italy.
Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Reggio Emilia, Italy.
Expert Rev Hematol. 2024 Jul;17(7):375-390. doi: 10.1080/17474086.2024.2357274. Epub 2024 May 21.
Therapeutic strategies against multiple myeloma (MM) have evolved dramatically in recent decades, with unprecedent results in the treatment landscape, culminating in the recent incorporation of novel agents in the anti-myeloma armamentarium.
BCMA represents one of the most promising targets in MM and currently available immune approaches, either approved or under active investigation, are clearly showing their greater potential over standard regimens. In this context, immunotherapies based on chimeric antigen receptor (CAR)-engineered T-cells and bispecific antibodies (BsAbs) have taken center stage, being the ones that are yielding the most promising results in clinical trials. This review focuses on the current landscape of BsAbs and CAR-T, summarizing the latest advances and possible future developments.
CAR-T and BsAbs anti-BCMA strategies represent breakthrough therapies against MM. However, their inclusion in clinical practice is almost feared, due to the associated limitations, some of which have been addressed here. Meanwhile, all the efforts should be focused on individualizing and choosing the most suitable candidates for each treatment and to understand how to combine, or sequence, these therapies to improve efficacy and minimize toxicity, especially for those patients with limited available treatment options.
近年来,针对多发性骨髓瘤(MM)的治疗策略有了显著的发展,在治疗领域取得了前所未有的成果,最近将新型药物纳入了抗骨髓瘤的治疗手段。
BCMA 是 MM 中最有前途的靶点之一,目前已批准或正在积极研究的免疫治疗方法显然显示出比标准方案更大的潜力。在这种情况下,基于嵌合抗原受体(CAR)修饰的 T 细胞和双特异性抗体(BsAb)的免疫疗法占据了中心位置,在临床试验中取得了最有前途的结果。这篇综述重点介绍了 BsAb 和 CAR-T 的最新进展,总结了最新的进展和可能的未来发展。
CAR-T 和 BsAb 抗 BCMA 策略是针对 MM 的突破性治疗方法。然而,由于其相关的局限性,它们在临床实践中的应用几乎令人恐惧,其中一些局限性已在这里得到解决。与此同时,所有的努力都应该集中在个体化和选择最适合每种治疗的患者上,并了解如何组合或序贯这些治疗方法,以提高疗效,最大限度地降低毒性,特别是对那些治疗选择有限的患者。