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新诊断的急性髓系白血病的风险适应性治疗策略:改善 ELN 2017 中危患者的结局。

Risk adapted therapeutic strategy in newly diagnosed acute myeloid leukemia: Refining the outcomes of ELN 2017 intermediate-risk patients.

机构信息

Hematology-Oncology Division, Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.

Hematopathology Division, Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Beirut, Lebanon.

出版信息

Leuk Res. 2021 Jun;105:106568. doi: 10.1016/j.leukres.2021.106568. Epub 2021 Mar 29.

Abstract

INTRODUCTION

Despite advances in the treatment of acute myeloid leukemia (AML), cytotoxic chemotherapy remains the standard induction regimen.

PATIENTS AND METHODS

In this single center retrospective study, we assessed outcomes of 99 consecutive adult AML patients treated with a risk-adapted strategy with a median follow-up of 35.5 months.

RESULTS

We identified 24 (24 %), 55 (56 %) and 20 (20 %) patients classified as favorable-, intermediate-, and adverse- risk group respectively, according to the European LeukemiaNet (ELN) 2017 classification. Patients either received idarubicin and cytarabine induction chemotherapy with or without FLT3 inhibitors or hypomethylating agents based on age and comorbidity. The complete response (CR) rate was 76 % (82 % and 61 % in patients aged < 60 and ≥ 60, respectively). For the whole cohort, the 3-year overall survival (OS) was 53 %, being 62 % and 30 % in patients aged < 60 and ≥ 60, respectively. The 3-year leukemia-free survival (LFS) was 54 %, with 56 % and 45 % in patients aged < 60 and ≥ 60, respectively. The 3-year LFS were 58 %, 62 % and 25 % for patients within ELN favorable-, intermediate-, and adverse-risk groups respectively. Twenty-seven (36 %) out of 75 patients with intermediate- and adverse-risk disease underwent allogeneic hematopoietic cell transplantation (allo-HCT) in first CR with 92 % of them receiving post-transplant maintenance consisting of azacitidine in 19 (76 %) patients or sorafenib in 6 (24 %) patients. Of these patients younger than 60 years, the 3-year OS and LFS were 85 % and 69 %, respectively.

CONCLUSION

These results indicate an improved OS for AML patients especially in intermediate-risk category who were treated with a total therapy consisting of induction chemotherapy followed by allo-HCT and post-transplant maintenance.

摘要

简介

尽管急性髓系白血病(AML)的治疗取得了进展,但细胞毒性化疗仍然是标准的诱导治疗方案。

患者和方法

在这项单中心回顾性研究中,我们评估了 99 例连续的成人 AML 患者采用风险适应策略的治疗结果,中位随访时间为 35.5 个月。

结果

根据欧洲白血病网(ELN)2017 分类,我们分别将 24 例(24%)、55 例(56%)和 20 例(20%)患者归类为低危、中危和高危组。根据年龄和合并症,患者接受阿糖胞苷联合去甲氧柔红霉素诱导化疗,或联合 FLT3 抑制剂或低甲基化药物。完全缓解(CR)率为 76%(年龄<60 岁和≥60 岁的患者分别为 82%和 61%)。对于整个队列,3 年总生存率(OS)为 53%,年龄<60 岁和≥60 岁的患者分别为 62%和 30%。3 年无白血病生存率(LFS)为 54%,年龄<60 岁和≥60 岁的患者分别为 56%和 45%。ELN 低危、中危和高危组患者的 3 年 LFS 分别为 58%、62%和 25%。27 例(36%)年龄在 60 岁及以上的中危和高危疾病患者在首次 CR 后接受了异基因造血细胞移植(allo-HCT),其中 92%的患者接受了阿扎胞苷(19 例,76%)或索拉非尼(6 例,24%)维持治疗。在这些年龄<60 岁的患者中,3 年 OS 和 LFS 分别为 85%和 69%。

结论

这些结果表明 AML 患者的 OS 得到了改善,特别是接受包括诱导化疗、allo-HCT 和移植后维持治疗在内的总治疗方案的中危患者。

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