Kuroda Junya
Division of Hematology and Oncology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine.
Rinsho Ketsueki. 2017;58(10):2058-2066. doi: 10.11406/rinketsu.58.2058.
The long-term outcome of multiple myeloma (MM) has been greatly improved by the advent of new agents such as proteasome inhibitors (PIs) and immunomodulatory drugs (IMiDs), despite the disease remaining mostly incurable. Treatment design is the critical determinant for the survival period and for the quality and way of life in patients with relapsed/refractory MM (RRMM). Recently, the choice of therapeutic options for RRMM has been expanded by the introduction of second generation PIs such as carfilzomib and ixazomib, and therapeutic monoclonal antibodies such as elotuzumab and daratumumab. In the choice of treatment strategies for RRMM, including stem cell transplantation, the decision should be based on an understanding of the characteristic clinical effects of each drug and the evaluation of the cytogenetic/molecular profile, myeloma-defining events, complications, and prior MM treatment history in individual patients.
尽管多发性骨髓瘤(MM)大多仍无法治愈,但蛋白酶体抑制剂(PIs)和免疫调节药物(IMiDs)等新型药物的出现已极大地改善了MM的长期预后。治疗方案的设计是复发/难治性MM(RRMM)患者生存期以及生活质量和方式的关键决定因素。最近,第二代PIs如卡非佐米和伊沙佐米,以及治疗性单克隆抗体如埃罗妥珠单抗和达雷妥尤单抗的引入,扩大了RRMM治疗选择的范围。在包括干细胞移植在内的RRMM治疗策略选择中,决策应基于对每种药物特征性临床疗效的了解,以及对个体患者细胞遗传学/分子谱、骨髓瘤定义事件、并发症和既往MM治疗史的评估。