Department of Clinical Therapeutics, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.
Department of Clinical Therapeutics, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.
Clin Lymphoma Myeloma Leuk. 2019 Jul;19(7):e324-e336. doi: 10.1016/j.clml.2019.03.008. Epub 2019 Apr 4.
Herein, we summarize the novel clinical data for multiple myeloma (MM) that were presented in the 2019 Annual Meeting of the American Society of Hematology. Triplet regimens including lenalidomide-dexamethasone for high-risk smoldering MM are effective but longer follow-up data are needed. Among transplant-eligible, newly diagnosed MM (NDMM) patients, carfilzomib- and daratumumab-based combinations are promising as effective and safe induction regimens and do not impair stem cell collection. Maintenance with ixazomib results in prolonged progression-free survival (PFS) compared with placebo. Regarding transplant-ineligible NDMM patients, large phase III studies showed that the additional use of daratumumab in backbone first-line regimens provides deep responses and PFS prolongation, whereas dose-/schedule-adjusted lenalidomide-dexamethasone has similar efficacy and is more tolerable than continuous lenalidomide-dexamethasone. In the relapsed/refractory setting carfilzomib- and daratumumab-based regimens remain highly effective and safe treatments, whereas the introduction of venetoclax, isatuximab, atezolizumab, and oprozomib broadens the therapeutic options. Among heavily pretreated MM patients, selinexor and melflufen showed particularly encouraging results. Novel immunotherapeutic approaches including chimeric antigen receptor T cells against B-cell maturation antigen and bispecific antibodies constitute a promising alternative that remains to be evaluated in later-phase studies.
在此,我们总结了在 2019 年美国血液学会年会上报告的多发性骨髓瘤(MM)的新临床数据。包含来那度胺-地塞米松的三联方案对于高危冒烟型 MM 是有效的,但需要更长时间的随访数据。对于适合移植的初诊 MM(NDMM)患者,基于卡非佐米和达雷妥尤单抗的联合方案作为有效的、安全的诱导方案具有前景,且不影响干细胞采集。与安慰剂相比,伊沙佐米维持治疗可延长无进展生存期(PFS)。对于不适合移植的 NDMM 患者,大型 III 期研究表明,在一线治疗方案中添加达雷妥尤单抗可提供更深层次的缓解和 PFS 延长,而剂量/方案调整的来那度胺-地塞米松与连续来那度胺-地塞米松具有相似的疗效且更耐受。在复发/难治性环境中,基于卡非佐米和达雷妥尤单抗的方案仍然是高度有效的治疗方法,而 venetoclax、isatuximab、atezolizumab 和 oprizo-mib 的引入拓宽了治疗选择。对于经过大量预处理的 MM 患者,selinexor 和 melflufen 显示出特别令人鼓舞的结果。新型免疫治疗方法包括针对 B 细胞成熟抗原的嵌合抗原受体 T 细胞和双特异性抗体,作为一种有前途的替代方案,仍需在后期研究中进行评估。