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环磷酰胺+依托泊苷+地塞米松作为挽救和桥接治疗方案用于复发难治和髓外多发性骨髓瘤。

Cyclophosphamide etoposide dexamethasone as salvage and bridging therapy in relapsed refractory and extramedullary multiple myeloma.

机构信息

Department of Haematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.

Molecular Medicine Partnership Unit (MMPU), Heidelberg, Germany.

出版信息

Hematol Oncol. 2023 Aug;41(3):453-462. doi: 10.1002/hon.3123. Epub 2023 Jan 26.

Abstract

Patients with relapsed refractory multiple myeloma (RRMM) that are triple-exposed to immunomodulatory drugs, proteasome inhibitors, and anti-CD38 monoclonal antibodies have a poor prognosis. Standard treatment for these patients has not been established. Patients with extramedullary disease or secondary plasma cell leukemia often display high tumor cell proliferation and might therefore be susceptible to chemotherapy. While current regimens are often platinum-based, we present single-center data on 70 patients with RRMM who were treated with cyclophosphamide, etoposide, and dexamethasone (CED) after a median of four lines of therapy. An overall response rate of 52% was achieved after 1-6 cycles, with 23% of patients having a very good partial response. Comparable response rates and survival were observed in patients with extramedullary disease and high-risk cytogenetics. Treatment resulted in non-hematological °III-IV adverse events in 31% of patients. No treatment-related deaths occurred. The median progression-free and overall survival were 6.2 and 10.9 months, respectively. 23% of patients were bridged to autologous stem cell transplantation (ASCT) or chimeric antigen receptor (CAR) T cell therapy. In summary, CED is an effective treatment regimen for RRMM cases with a tolerable safety profile and suitable as bridging therapy to CAR T cell treatment and ASCT.

摘要

对于三重暴露于免疫调节药物、蛋白酶体抑制剂和抗 CD38 单克隆抗体的复发性难治性多发性骨髓瘤 (RRMM) 患者,预后较差。这些患者的标准治疗尚未建立。有骨髓外疾病或继发性浆细胞白血病的患者通常表现出高肿瘤细胞增殖,因此可能容易受到化疗的影响。虽然目前的方案通常基于铂类药物,但我们提供了来自单中心的数据,该数据涉及 70 名 RRMM 患者,他们在接受中位数为四线治疗后接受了环磷酰胺、依托泊苷和地塞米松 (CED) 治疗。在 1-6 个周期后,总缓解率达到 52%,23%的患者有非常好的部分缓解。在有骨髓外疾病和高风险细胞遗传学的患者中观察到了相似的缓解率和生存率。治疗导致 31%的患者出现非血液学 °III-IV 级不良事件。无治疗相关死亡。中位无进展生存期和总生存期分别为 6.2 和 10.9 个月。23%的患者接受了自体干细胞移植 (ASCT) 或嵌合抗原受体 (CAR) T 细胞治疗的桥接。总之,CED 是 RRMM 患者的一种有效治疗方案,具有可耐受的安全性特征,适合作为 CAR T 细胞治疗和 ASCT 的桥接治疗。

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