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Investigational agents in immunotherapy: a new horizon for the treatment of multiple myeloma

机译:免疫治疗中的研究药剂:一种用于治疗多发性骨髓瘤的新地平线

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Summary The treatment of multiple myeloma ( MM ) has gone through several major advances over the last 5?years with the introduction of next generation proteasome inhibitors ( PI ; carfilzomib, ixazomib) and immunomodulatory derivatives ( IM iD; pomalidomide), with these new agents having a substantial impact on patient outcome. However, despite these advances, MM remains a highly resistant disease given its propensity for clonal heterogeneity and its complex interaction with the surrounding bone marrow microenvironment. Almost all patients eventually relapse despite therapeutic responses to a PI , IM iD or both. With the regulatory approval of the monoclonal antibodies Daratumumab and Elotuzumab in 2015, impressive and durable responses are being observed, even in heavily pre‐treated patients who have exhausted other therapeutic options, suggesting immunological approaches in this setting have real merit. This review will focus on newer monoclonal antibodies and chimeric‐antigen receptor ( CAR ) T cell strategies currently under investigation and in various stages of clinical development.
机译:发明内容多发性骨髓瘤(MM)的治疗经历了过去5岁以下的几个主要进步随着下一代蛋白酶体抑制剂(PI; Carfilzomib,Ixazomib)和免疫调节衍生物(IM ID;氯胺),具有这些新试剂对患者结果有很大的影响。然而,尽管这些进展,MM仍然是耐粘性异质性的倾向和与周围骨髓微环境的复杂相互作用的倾向致力耐药性。尽管治疗对PI,IM ID或两者的治疗反应,但所有患者最终都会复发。通过2015年单克隆抗体的监管批准,2015年,令人印象深刻和耐用的反应,即使在大量预处理的患者中疲惫不堪的患者,也表明该环境中的免疫学方法具有真实的优点。本综述将专注于目前正在调查和临床发展的各个阶段的较新的单克隆抗体和嵌合抗原受体(CAR)T细胞策略。

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