Chakrabarti Ritu, Siegel David, Biran Noa
Hackensack Meridian Health, Jersey Shore University Medical Center, Neptune Township, NJ.
Hackensack Meridian Health, John Theurer Cancer Center, Hackensack, NJ.
Clin Lymphoma Myeloma Leuk. 2025 Feb;25(2):96-108. doi: 10.1016/j.clml.2024.08.004. Epub 2024 Aug 8.
Multiple myeloma (MM) is a plasma cell dyscrasia characterized by production of abnormal levels of a monoclonal immunoglobulin or plasma cell deposition that leads to end organ destruction. The disease remains incurable despite advances in combination treatments with classes of medications that include proteosome inhibitors, immunomodulating agents, monoclonal antibodies, small molecule inhibitors, alkylating agents, T-cell-based immunotherapies, and others. Checkpoint inhibitors (CKP-I), though showing robust efficacy in solid tumor and lymphoma, have had limited success as single agents in the treatment of MM. Furthermore, early FDA holds on trials involving CKP-I in myeloma led to diminished enrollment and data on its potential use. Nevertheless, clearer understanding of the mechanisms of immune dysregulation and unique bone marrow biology in the pathophysiology of MM have opened the opportunity for future uses of CKP-I in multiple myeloma. Herein we provide a comprehensive review of the immunologic basis of multiple myeloma, preclinical and published data from trials utilizing CKP-I in MM patients, and future targets in CKP-I development that may provide promising opportunities in the treatment of MM.
多发性骨髓瘤(MM)是一种浆细胞异常增生性疾病,其特征是单克隆免疫球蛋白水平异常升高或浆细胞沉积,导致终末器官破坏。尽管在联合使用包括蛋白酶体抑制剂、免疫调节剂、单克隆抗体、小分子抑制剂、烷化剂、基于T细胞的免疫疗法等各类药物进行治疗方面取得了进展,但该疾病仍然无法治愈。检查点抑制剂(CKP-I)虽然在实体瘤和淋巴瘤中显示出强大的疗效,但作为单一药物治疗MM的成功率有限。此外,美国食品药品监督管理局(FDA)早期对涉及CKP-I治疗骨髓瘤的试验进行的审查导致入组人数减少,以及关于其潜在用途的数据也有所减少。然而,对MM病理生理学中免疫失调机制和独特骨髓生物学的更清晰理解为CKP-I未来在多发性骨髓瘤中的应用开辟了机会。在此,我们全面综述了多发性骨髓瘤的免疫学基础、在MM患者中使用CKP-I的临床前和已发表的试验数据,以及CKP-I开发中的未来靶点,这些靶点可能为MM治疗提供有前景的机会。