[Novel therapeutic approaches for multiple myeloma].

Kyoko Yoshihara
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引用次数: 0

Abstract

Multiple myeloma has conventionally been treated with three major classes of drugs, including immunomodulatory drugs, proteasome inhibitors and anti-CD38 antibodies, but T-cell redirection therapies (CAR-T cell therapy and bispecific antibodies) targeting B-cell maturation antigen (BCMA), which is highly expressed on the surface of myeloma cells, have now been adopted as a new modality. In Japan, CAR-T therapy is indicated as a third-line treatment for patients who have already received three classes of drugs, and bispecific antibodies are also indicated for patients who have already received three lines of therapy. Regimens combining antibody-drug conjugates targeting BCMA with bortezomib or pomalidomide have also demonstrated efficacy. GPRC5D is also attracting attention as a new target, and bispecific antibodies should soon become available for clinical use. Although these are very effective treatments, they are not curative. Therefore, determining how to sequence conventional treatments (combinations of the three classes) and these new treatments will be an important clinical challenge.

多发性骨髓瘤的新治疗方法。
多发性骨髓瘤的治疗传统上主要有三大类药物,包括免疫调节药物、蛋白酶体抑制剂和抗cd38抗体,但针对骨髓瘤细胞表面高表达的b细胞成熟抗原(BCMA)的t细胞重定向疗法(CAR-T细胞疗法和双特异性抗体)现在已被采用为一种新的治疗方式。在日本,CAR-T疗法被认为是已经接受了三种药物治疗的患者的三线治疗,双特异性抗体也被认为是已经接受了三种药物治疗的患者的三线治疗。靶向BCMA的抗体-药物偶联药物与硼替佐米或泊马度胺联合治疗也已证明有效。GPRC5D作为一种新的靶点也引起了人们的关注,双特异性抗体应该很快就可以用于临床。虽然这些都是非常有效的治疗方法,但它们并不能治愈。因此,确定如何对常规治疗(三种药物的组合)和这些新治疗进行排序将是一项重要的临床挑战。
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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