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FLAG-Ida 与柔红霉素联合克拉屈滨治疗复发或难治性急性髓系白血病的随机比较:来自英国 NCRI AML17 试验的结果。

A randomised comparison of FLAG-Ida versus daunorubicin combined with clofarabine in relapsed or refractory acute myeloid leukaemia: Results from the UK NCRI AML17 trial.

机构信息

Department of Haematology, Guy's Hospital, London, UK.

Nuffield Department of Population Health, University of Oxford, Oxford, UK.

出版信息

Br J Haematol. 2022 Aug;198(3):528-534. doi: 10.1111/bjh.18195. Epub 2022 Apr 6.

DOI:10.1111/bjh.18195
PMID:35388465
Abstract

The prognosis for younger patients with relapsed acute myeloid leukaemia (AML) is generally dismal. Allogeneic stem cell transplantation is the preferred therapy for these patients. As part of the UK NCRI AML17 trial, daunorubicin/clofarabine (DClo) was compared with fludarabine, cytarabine, granulocyte colony-stimulating factor with idarubicin (FLAG-Ida) in 311 patients designated high-risk following course one of induction therapy, which has previously been reported. We now report the results of the same randomisation in patients who were refractory to two induction courses or subsequently relapsed. A total of 94 relapsed or refractory AML patients, usually less than 60 years of age and with mainly favourable or intermediate-risk cytogenetics, were randomised to receive up to three courses of DClo or FLAG-Ida, with the aim of proceeding to transplant. Complete remission was achieved in 74% of patients with no difference between the arms. Overall, 57% of patients received a transplant with no difference between the arms, likewise overall survival at five years showed no significant difference (21% for DClo vs. 22% for FLAG-Ida). No patient who did not receive a transplant survived beyond 21months. A stratified analysis including the 311 post course 1 high-risk patients who underwent the same randomisation showed a consistent treatment benefit for FLAG-Ida.

摘要

对于复发的急性髓系白血病(AML)年轻患者,预后通常较差。异基因造血干细胞移植是这些患者的首选治疗方法。在英国 NCRI AML17 试验中,阿糖胞苷、柔红霉素/克拉屈滨(DClo)与氟达拉滨、阿糖胞苷、粒细胞集落刺激因子与伊达比星(FLAG-Ida)在 311 名被指定为诱导治疗第一疗程后高危的患者中进行了比较,这在之前已有报道。我们现在报告了在对两个诱导疗程耐药或随后复发的患者中进行相同随机分组的结果。共有 94 例复发或难治性 AML 患者,通常年龄小于 60 岁,且主要具有有利或中等风险的细胞遗传学特征,他们被随机分配接受多达三个疗程的 DClo 或 FLAG-Ida,目的是进行移植。完全缓解率为 74%,两组之间无差异。总体而言,57%的患者接受了移植,两组之间无差异,同样,五年总生存率也没有显著差异(DClo 为 21%,FLAG-Ida 为 22%)。没有未接受移植的患者存活超过 21 个月。一项包括 311 名接受相同随机分组的第一疗程后高危患者的分层分析显示,FLAG-Ida 有一致的治疗益处。

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