de Arriba de la Fuente Felipe, Montes Gaisán Carmen, de la Rubia Comos Javier
Haematology and Medical Oncology Department, Hospital General Universitario Morales Meseguer, Instituto Murciano de Investigación Biomédica (IMIB)-Arrixaca, Universidad de Murcia, 30008 Murcia, Spain.
Haematology Department, Hospital Universitario Marqués de Valdecilla, 39008 Cantabria, Spain.
Cancers (Basel). 2022 Dec 27;15(1):155. doi: 10.3390/cancers15010155.
Although lenalidomide-based combinations, such as lenalidomide plus a proteasome inhibitor or an anti-CD38 monoclonal antibody, improve the overall response rate, progression-free survival, and overall survival of patients with relapsed/refractory multiple myeloma (RRMM), there is a tendency to use these regimens as a frontline treatment. This strategy has led to the development of refractoriness early in the disease course, usually after the patient's first treatment. Since lenalidomide-free regimens have so far shown limited efficacy in lenalidomide-refractory patients, there is an unmet need for other treatment options. In this review, we discuss the therapeutic options available to treat the general population of lenalidomide-refractory patients (mono, double and triple refractory) and the subpopulation of patients with other high-risk features such as renal failure, extramedullary disease, and high-risk cytogenetics. Moreover, new promising individual therapies and the possible impact of immunotherapy in RRMM patients are debated.
尽管基于来那度胺的联合方案,如来那度胺联合蛋白酶体抑制剂或抗CD38单克隆抗体,可提高复发/难治性多发性骨髓瘤(RRMM)患者的总缓解率、无进展生存期和总生存期,但目前存在将来那度胺方案用作一线治疗的趋势。这种策略导致在疾病进程早期,通常是在患者首次治疗后就出现难治性。由于不含来那度胺的方案迄今在来那度胺难治性患者中显示出有限的疗效,因此对其他治疗选择存在未满足的需求。在本综述中,我们讨论了可用于治疗来那度胺难治性患者总体人群(单药难治、双药难治和三药难治)以及具有其他高危特征(如肾衰竭、髓外疾病和高危细胞遗传学)患者亚群的治疗选择。此外,还讨论了新的有前景的个体化疗法以及免疫疗法对RRMM患者可能产生的影响。