Palumbo Antonio, Sonneveld Pieter
Myeloma Unit, Division of Haematology, University of Turin, Turin, Italy.
Expert Rev Hematol. 2015 Aug;8(4):481-91. doi: 10.1586/17474086.2015.1053866. Epub 2015 Jun 12.
Although multiple myeloma has historically been treated with chemotherapy, prolonged survival has only been possible since the introduction of thalidomide, lenalidomide and bortezomib. However, multiple myeloma remains largely incurable, and new treatments are needed to improve long-term outcome. Elotuzumab is a humanized IgG1 monoclonal antibody that targets Signaling Lymphocyte Activation Molecule Family member 7 (SLAMF7) to activate NK cells, enabling selective killing of myeloma cells with minimal effects on normal tissue. The combination of elotuzumab with antimyeloma therapies that stimulate host immunity may be an attractive treatment option for patients with newly diagnosed or relapsed/refractory multiple myeloma. Here, we review the role of SLAMF7 in the pathogenesis of multiple myeloma and the preclinical and clinical development of elotuzumab.
尽管多发性骨髓瘤在历史上一直采用化疗进行治疗,但自沙利度胺、来那度胺和硼替佐米引入后才实现了长期生存。然而,多发性骨髓瘤在很大程度上仍然无法治愈,需要新的治疗方法来改善长期疗效。埃罗妥珠单抗是一种人源化IgG1单克隆抗体,其靶向信号淋巴细胞激活分子家族成员7(SLAMF7)以激活自然杀伤(NK)细胞,从而能够在对正常组织影响最小的情况下选择性杀伤骨髓瘤细胞。埃罗妥珠单抗与刺激宿主免疫的抗骨髓瘤疗法联合使用,可能是新诊断或复发/难治性多发性骨髓瘤患者的一种有吸引力的治疗选择。在此,我们综述了SLAMF7在多发性骨髓瘤发病机制中的作用以及埃罗妥珠单抗的临床前和临床开发情况。