Ozaki Shuji
Department of Hematology, Tokushima Prefectural Central Hospital.
Rinsho Ketsueki. 2018;59(10):2178-2188. doi: 10.11406/rinketsu.59.2178.
The development of novel agents for treating multiple myeloma (MM) has markedly improved the treatment outcome and has caused a major paradigm shift in treatment strategies. In Japan, bortezomib and lenalidomide have been approved for the initial treatment; additionally, seven novel drugs, including next-generation proteasome inhibitors, immunomodulatory drugs, histone deacetylase inhibitors, and monoclonal antibodies, have been approved for relapsed and/or refractory MM treatment. Of these novel agents, daratumumab-containing regimens have been reported to induce a deep response, such as minimal residual disease-negative status, even in relapsed patients. Thus, compared with the initial therapy, many efficacious choices are available for treatment at the time of MM relapse; and salvage therapy is currently considered to be the most important treatment strategy for MM. In clinical practice, it is desirable to consider patient, disease, and therapeutic factors to make an optimal treatment decision for each patient.
用于治疗多发性骨髓瘤(MM)的新型药物的研发显著改善了治疗效果,并在治疗策略上引发了重大的模式转变。在日本,硼替佐米和来那度胺已被批准用于初始治疗;此外,包括下一代蛋白酶体抑制剂、免疫调节药物、组蛋白去乙酰化酶抑制剂和单克隆抗体在内的七种新型药物已被批准用于复发和/或难治性MM的治疗。在这些新型药物中,据报道含达雷妥尤单抗的方案即使在复发患者中也能诱导深度缓解,如微小残留病阴性状态。因此,与初始治疗相比,MM复发时可供选择的有效治疗方案更多;目前挽救性治疗被认为是MM最重要的治疗策略。在临床实践中,需要综合考虑患者、疾病和治疗因素,为每位患者做出最佳治疗决策。