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米托蒽醌、依托泊苷和阿糖胞苷治疗复发或难治性急性髓系白血病的疗效和安全性。

Efficacy and safety of mitoxantrone, etoposide, and cytarabine for treatment of relapsed or refractory acute myeloid leukemia.

机构信息

Department of Pharmacy, Cleveland Clinic, 9500 Euclid Ave, Cleveland, OH 44195, USA.

Department of Pharmacy, Cleveland Clinic, 9500 Euclid Ave, Cleveland, OH 44195, USA.

出版信息

Leuk Res. 2024 Apr;139:107468. doi: 10.1016/j.leukres.2024.107468. Epub 2024 Feb 27.

Abstract

BACKGROUND/RATIONALE: Most patients with acute myeloid leukemia (AML) develop relapsed or refractory (R/R) disease after receiving initial induction chemotherapy. Salvage chemotherapy followed by allogeneic hematopoietic stem cell transplantation (alloHSCT) is the only curative therapy for R/R AML. Mitoxantrone, etoposide, and cytarabine (MEC) is the current standard of care salvage regimen for R/R AML at Cleveland Clinic. The primary objective was to determine the overall remission rate (ORR: defined as patients achieving complete remission (CR) or complete remission with incomplete hematologic recovery (CRi)) in R/R AML patients who received MEC.

METHODS

Adult patients with R/R AML treated with MEC between July 1, 2014 and September 30, 2022 were included. ORR and its association with baseline characteristics were determined. Secondary outcomes included overall survival (OS), event-free survival (EFS), relapse-free survival (RFS), and safety.

RESULTS

Sixty patients were evaluated. The ORR was 51.7% (33.3% CR and 18.3% CRi). The median time from receipt of MEC to CR/CRi was 7.7 weeks. Patients with bone marrow blasts ≤20% and peripheral blood blasts ≤30% at MEC initiation were more than twice as likely to achieve CR/CRi compared to those with a higher blast burden. The median OS was 6.3 months. Twenty-four (40.0%) patients proceeded to alloHSCT. Twenty-one (35.0%) patients were transferred to the intensive care unit (ICU) during their admission.

CONCLUSIONS

MEC is an effective salvage regimen for patients with R/R AML, especially among those with low disease burden at initiation. Febrile neutropenia, infections, and severe oral mucositis were common with MEC administration.

摘要

背景/理由:大多数急性髓系白血病(AML)患者在接受初始诱导化疗后会发展为复发或难治性(R/R)疾病。挽救性化疗后进行异基因造血干细胞移植(alloHSCT)是 R/R AML 的唯一治愈性治疗方法。米托蒽醌、依托泊苷和阿糖胞苷(MEC)是克利夫兰诊所目前 R/R AML 的标准挽救治疗方案。主要目的是确定接受 MEC 治疗的 R/R AML 患者的总缓解率(ORR:定义为达到完全缓解(CR)或不完全血液学恢复的完全缓解(CRi)的患者)。

方法

纳入 2014 年 7 月 1 日至 2022 年 9 月 30 日期间接受 MEC 治疗的 R/R AML 成年患者。确定 ORR 及其与基线特征的关系。次要结局包括总生存期(OS)、无事件生存期(EFS)、无复发生存期(RFS)和安全性。

结果

对 60 例患者进行了评估。ORR 为 51.7%(33.3%CR 和 18.3%CRi)。从接受 MEC 到获得 CR/CRi 的中位时间为 7.7 周。在 MEC 开始时骨髓原始细胞≤20%和外周血原始细胞≤30%的患者,与原始细胞负荷较高的患者相比,获得 CR/CRi 的可能性高出两倍以上。中位 OS 为 6.3 个月。24 例(40.0%)患者进行 alloHSCT。21 例(35.0%)患者在住院期间转入重症监护病房(ICU)。

结论

MEC 是 R/R AML 患者的有效挽救治疗方案,尤其是在疾病负担较低的患者中。发热性中性粒细胞减少症、感染和严重口腔粘膜炎是 MEC 治疗的常见并发症。

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