Combined Proteasome and Autophagy Inhibition in Relapsed/Refractory Multiple Myeloma-A Phase I Trial of Hydroxychloroquine, Carfilzomib, and Dexamethasone.

EJHaem Pub Date : 2025-01-23 eCollection Date: 2025-02-01 DOI:10.1002/jha2.1091
Tobias S Slørdahl, Frida Bugge Askeland, Margrete Sofie Sætre Hanssen, Håkon Hov, Stine Marie Sundt-Hansen, Sofia Lindahl, Nils Tore Vethe, Henrik Hjorth-Hansen, Mona H Fenstad, Anders Waage, Øyvind Hjertner, Fredrik Schjesvold, Anders Sundan
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Abstract

Multiple myeloma is characterized by malignant cells which produce high amounts of monoclonal immunoglobulin. Myeloma cells are, therefore, dependent on effective protein degradation. Proteasomal protein degradation is targeted by proteasome inhibitors in routine care. Autophagic protein degradation is currently not targeted in myeloma treatment. This Phase I trial showed that the combination of the proteasome inhibitor carfilzomib and the autophagy inhibitor hydroxychloroquine was well tolerated in patients with relapsed/refractory multiple myeloma. Adverse events were mostly Grades 1 and 2. An overall response rate of 44% indicates a meaningful clinical efficacy of this combination. Trial Registration: The study was registered at clinicaltrials.gov # NCT04163107.

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多发性骨髓瘤的特征是恶性细胞产生大量单克隆免疫球蛋白。因此,骨髓瘤细胞依赖于有效的蛋白质降解。在常规治疗中,蛋白酶体抑制剂主要针对蛋白酶体蛋白降解。自噬蛋白降解目前还不是骨髓瘤治疗的目标。这项I期试验表明,复发/难治性多发性骨髓瘤患者对蛋白酶体抑制剂卡非佐米和自噬抑制剂羟氯喹的联合治疗耐受性良好。不良反应大多为1级和2级。总体应答率为44%,表明这种组合具有显著的临床疗效。试验注册:该研究已在 clinicaltrials.gov # NCT04163107 上注册。
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