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复发性或难治性急性髓系白血病患者接受 Mito-FLAG 挽救化疗的结果。

Outcome of patients with relapsed or refractory acute myeloid leukemia treated with Mito-FLAG salvage chemotherapy.

机构信息

Klinik für Innere Medizin II, Abteilung für Hämatologie und Internistische Onkologie, Universitätsklinikum Jena, Am Klinikum 1, 07747, Jena, Germany.

4. Medizinische Klinik, HELIOS Klinikum Erfurt, Nordhäuser Straße 74, 99089, Erfurt, Germany.

出版信息

J Cancer Res Clin Oncol. 2022 Sep;148(9):2539-2548. doi: 10.1007/s00432-021-03821-1. Epub 2021 Oct 5.

Abstract

PURPOSE

Curative intended treatment is challenging in patients with relapsed or refractory acute myeloid leukemia (r/r AML) and associated with a dismal prognosis for long-term survival. Despite novel treatment options, the majority of patients are treated with chemotherapy-based regimens. Although widely used, little data exist on the combination of fludarabine, cytarabine, granulocyte colony stimulating factor (FLAG) and mitoxantrone as salvage strategy for r/r AML.

MATERIALS AND METHODS

Sixty-six patients receiving Mito-FLAG for r/r AML treated at a German tertiary care center between 2009 and 2019 were analyzed with regard to response rates, survival and safety profile.

RESULTS

Overall response rate was 75.8% with 56.1% of patients achieving complete remission (CR) and 19.7% partial remission (PR). After a median follow-up of 54 months, median overall survival (OS) was 13 months. Patients transitioned to allogeneic hematopoietic stem cell transplantation (alloHSCT) (75.8%) showed a significant improvement in OS with a median OS of 17 (95% CI 8.5-25.4) months vs 3 (95% CI 1.7-4.3) months (p < 0.001). 30- and 60-day mortality rates for all patients after the initial cycle of Mito-FLAG were 4.5% and 7.6%, respectively.

CONCLUSION

The Mito-FLAG salvage protocol represents an effective and feasible treatment regimen for r/r AML. Importantly, a high rate of transition to successful alloHSCT with the aim of long-term disease-free survival has been shown.

摘要

目的

复发或难治性急性髓系白血病(r/r AML)患者的治愈性治疗具有挑战性,其长期生存预后较差。尽管有新的治疗选择,但大多数患者仍接受基于化疗的方案治疗。尽管广泛应用,但关于氟达拉滨、阿糖胞苷、粒细胞集落刺激因子(FLAG)和米托蒽醌联合作为 r/r AML 挽救策略的数据很少。

材料和方法

对 2009 年至 2019 年期间在德国三级医疗中心接受米托蒽醌-FLAG 治疗的 66 例 r/r AML 患者的反应率、生存和安全性进行了分析。

结果

总反应率为 75.8%,56.1%的患者达到完全缓解(CR),19.7%的患者达到部分缓解(PR)。中位随访 54 个月后,中位总生存期(OS)为 13 个月。接受异基因造血干细胞移植(alloHSCT)(75.8%)的患者 OS 显著改善,中位 OS 为 17 个月(95%CI 8.5-25.4),而 3 个月(95%CI 1.7-4.3)(p<0.001)。所有患者初始米托蒽醌-FLAG 治疗后 30 天和 60 天死亡率分别为 4.5%和 7.6%。

结论

米托蒽醌-FLAG 挽救方案是治疗 r/r AML 的有效且可行的治疗方案。重要的是,已经显示出很高的成功率转化为成功的 alloHSCT,以实现长期无病生存。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9648/11800820/f4ae38c0a2de/432_2021_3821_Fig1_HTML.jpg

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