Tracy Murphy,Boyang Zhang,Tong Zhang,Ian King,Jose-Mario Capo-Chichi,Vikas Gupta,Dawn Maze,Caroline J McNamara,Mark D Minden,Aaron D Schimmer,Andre C Schuh,Hassan Sibai,Karen W L Yee,Andrea Arruda,Zhibin Lu,Dina Khalaf,Chantal Rockwell,Brian Leber,Mitchell Sabloff,Anne Tierens,Tracy L Stockley,Steven M Chan,Stanley W K Ng,Jean C Y Wang
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引用次数: 0
摘要
急性髓性白血病(AML)患者表现出不同的分子和细胞遗传学变化和不同的结果。功能来源的LSC17基因表达评分在成人和儿童AML队列的回顾性分析中显示出很强的预后意义,在强化治疗的患者中,高于中位数的评分与低于中位数的评分相比,预后更差。在此,我们使用实验室开发的临床验证的基于nanostring的LSC17检测方法,在276例新诊断的AML患者的前瞻性多中心研究中测试LSC17评分的预后价值。通过与先前建立的参考评分进行比较,每个患者的评分被分为高或低。在整个队列中,高LSC17评分与较差的风险特征相关,包括高龄和不利的基因突变。在接受强化治疗的190例患者中,高LSC17评分与较低的缓解率相关(诱导后为63% vs 94%, P。
Real-world validation study of the LSC17 score for risk prediction in patients with newly diagnosed acute myeloid leukemia.
Acute myeloid leukemia (AML) patients exhibit diverse molecular and cytogenetic changes with heterogeneous outcomes. The functionally-derived LSC17 gene expression score has demonstrated strong prognostic significance in retrospective analyses of adult and pediatric AML cohorts, where above-median scores are associated with worse outcomes compared to below-median scores in intensively-treated patients. Here we used a laboratory-developed clinically-validated NanoStringbased LSC17 assay to test the prognostic value of the LSC17 score in a prospective multicentre study of 276 newly-diagnosed AML patients. Each patient's score was classified as high or low by comparison to a previously-established reference score. In the entire cohort, a high LSC17 score was associated with poor risk features, including advanced age and unfavorable genetic mutations. In the subset of 190 patients treated intensively, a high LSC17 score was associated with lower remission rates (63% vs 94% after induction, P.
期刊介绍:
Haematologica is a journal that publishes articles within the broad field of hematology. It reports on novel findings in basic, clinical, and translational research.
Scope:
The scope of the journal includes reporting novel research results that:
Have a significant impact on understanding normal hematology or the development of hematological diseases.
Are likely to bring important changes to the diagnosis or treatment of hematological diseases.