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FLT3(ITD) 突变等位基因水平对中危急性髓系白血病复发风险的影响。

Impact of FLT3(ITD) mutant allele level on relapse risk in intermediate-risk acute myeloid leukemia.

机构信息

Department of Haematology, University College London Cancer Institute, London, United Kingdom; and.

Department of Haematology, Cardiff University School of Medicine, Cardiff, United Kingdom.

出版信息

Blood. 2014 Jul 10;124(2):273-6. doi: 10.1182/blood-2014-02-554667. Epub 2014 May 22.

Abstract

Some studies have suggested that cases of acute myeloid leukemia (AML) with low levels of FLT3 internal tandem duplications (FLT3(ITD)) do not have a worse prognosis if there is a concomitant NPM1 mutation, although this is controversial. To clarify this therapeutically important issue, we have analyzed FLT3(ITD) and NPM1(MUT) levels in 1609 younger adult cases of cytogenetically intermediate-risk AML. The cumulative incidence of relapse was increased in NPM1(MUT) cases by the presence of a FLT3(ITD), but did not differ markedly according to FLT3(ITD) level. This remained true when allowance was made for poor leukemic cell purity by adjustment of the FLT3(ITD) level to the measured NPM1(MUT) level. If consolidation therapies are to be determined by relapse risk, then NPM1(MUT) cases with low-level FLT3(ITD) should not be considered as good risk without further studies. AML 12 and AML 15 are registered at http://www.controlled-trials.com under ISRCTN17833622 and ISRCTN17161961, respectively.

摘要

一些研究表明,如果伴有 NPM1 突变,低水平 FLT3 内部串联重复(FLT3(ITD))的急性髓系白血病(AML)病例的预后并不差,但这存在争议。为了阐明这个具有重要治疗意义的问题,我们分析了 1609 例细胞遗传学中危 AML 年轻成年患者的 FLT3(ITD)和 NPM1(MUT)水平。NPM1(MUT)病例中存在 FLT3(ITD)会增加复发的累积发生率,但根据 FLT3(ITD)水平并无显著差异。当通过调整 FLT3(ITD)水平以适应测量的 NPM1(MUT)水平来考虑白血病细胞纯度较差时,这仍然是正确的。如果巩固治疗要根据复发风险来确定,那么没有进一步的研究,就不应该将低水平 FLT3(ITD)的 NPM1(MUT)病例视为低危。AML 12 和 AML 15 分别在 http://www.controlled-trials.com 上注册,注册号为 ISRCTN12 和 ISRCTN17。

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