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环磷酰胺、依托泊苷、地塞米松作为复发/难治性及髓外多发性骨髓瘤的挽救与桥接治疗

英文原题:Cyclophosphamide etoposide dexamethasone as salvage and bridging therapy in relapsed refractory and extramedullary multiple myeloma.

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

PubMed 2023/01/26(内容时间) Hematol Oncol Q1 · IF 4.1(JCR 2025)

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中文摘要

对于既往接受过免疫调节药物、蛋白酶体抑制剂和抗CD38单克隆抗体三类药物治疗的复发/难治性多发性骨髓瘤(RRMM)患者,预后较差,目前尚无确立的标准治疗。髓外病变或继发性浆细胞白血病患者常表现出较高的肿瘤细胞增殖,因而可能对化疗敏感。当前方案通常以铂类药物为基础;本文报告单中心70例RRMM患者的数据,这些患者在中位接受四线治疗后接受了环磷酰胺、依托泊苷和地塞米松(CED)治疗。经过1–6个周期治疗后,总缓解率为52%,其中23%的患者达到非常好的部分缓解。髓外病变患者与具有高危细胞遗传学特征的患者,缓解率和生存结局相近。治疗导致31%的患者出现非血液学III–IV级不良事件,未发生治疗相关死亡。中位无进展生存期和总生存期分别为6.2个月和10.9个月。23%的患者后续接受自体造血干细胞移植(ASCT)或嵌合抗原受体(CAR)T细胞治疗。

总之,CED对RRMM有效,安全性可耐受,并适合作为CAR-T 细胞治疗和ASCT的桥接治疗。

展开英文摘要原文

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.

论文信息

作者
Kauer J、Sester LS、Kriegsmann K、Weinhold N、Ober M、Müller-Tidow C、Goldschmidt H、Raab MS
单位
Department of Haematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.Germany
期刊
Hematological oncology2023 Aug
原文标识
PubMed 36680428 · DOI 10.1002/hon.3123