Ozaki Shuji
Department of Hematology, Tokushima Prefectural Central Hospital.
Rinsho Ketsueki. 2017;58(8):1014-1023. doi: 10.11406/rinketsu.58.1014.
Recent progress in the development of novel therapeutic agents has remarkably improved the treatment outcome for multiple myeloma (MM). Proteasome inhibitors such as bortezomib, carfilzomib, and ixazomib; immunomodulatory drugs (IMiDs) such as thalidomide, lenalidomide, and pomalidomide; the histone deacetylase (HDAC) inhibitor panobinostat; and the monoclonal antibody, elotuzumab, have all been approved in Japan, although only bortezomib and lenalidomide have been approved for initial therapy. Accordingly, the Japanese Society of Hematology has released updated treatment guidelines for MM. Initial treatments with bortezomib-based 2-3 drug regimens and lenalidomide+dexamethasone are recommended for patients eligible for autologous stem cell transplantation (ASCT), while bortezomib+melphalan+prednisolone and lenalidomide+dexamethasone are recommended for patients who are not eligible for ASCT. These novel agents provide us with wider therapeutic options for relapsed or refractory patients. Consequently, treatment paradigms for MM continue to rapidly evolve, and it is important to select the optimal treatment strategy for each patient.
新型治疗药物研发的最新进展显著改善了多发性骨髓瘤(MM)的治疗效果。蛋白酶体抑制剂如硼替佐米、卡非佐米和伊沙佐米;免疫调节药物(IMiDs)如沙利度胺、来那度胺和泊马度胺;组蛋白去乙酰化酶(HDAC)抑制剂帕比司他;以及单克隆抗体埃罗妥珠单抗,在日本均已获批,不过只有硼替佐米和来那度胺被批准用于初始治疗。因此,日本血液学会发布了MM的更新治疗指南。对于适合自体干细胞移植(ASCT)的患者,推荐使用基于硼替佐米的2 - 3药方案和来那度胺+地塞米松进行初始治疗,而对于不适合ASCT的患者,推荐使用硼替佐米+美法仑+泼尼松和来那度胺+地塞米松。这些新型药物为复发或难治性患者提供了更广泛的治疗选择。因此,MM的治疗模式在持续快速演变,为每位患者选择最佳治疗策略非常重要。