累积发病率
危险系数
髓系白血病
内科学
医学
肿瘤科
CD38
川地34
白血病
干细胞
净现值1
骨髓
髓样
胃肠病学
移植
生物
置信区间
基因
生物化学
遗传学
核型
染色体
作者
Wendelien Zeijlemaker,Tim Grob,Rosa J. Meijer,Diana Hanekamp,Angèle Kelder,Jannemieke Carbaat‐Ham,Yvonne J.M Oussoren-Brockhoff,Alexander N. Snel,Dennis Veldhuizen,Willemijn J. Scholten,Johan Maertens,Dimitri Breems,Thomas Pabst,Markus G. Manz,Vincent H. J. van der Velden,Jennichjen Slomp,Frank Preijers,Jacqueline Cloos,Arjan A. van de Loosdrecht,Bob Löwenberg
出处
期刊:Leukemia
[Springer Nature]
日期:2018-12-12
卷期号:33 (5): 1102-1112
被引量:204
标识
DOI:10.1038/s41375-018-0326-3
摘要
Current risk algorithms are primarily based on pre-treatment factors and imperfectly predict outcome in acute myeloid leukemia (AML). We introduce and validate a post-treatment approach of leukemic stem cell (LSC) assessment for prediction of outcome. LSC containing CD34+CD38− fractions were measured using flow cytometry in an add-on study of the HOVON102/SAKK trial. Predefined cut-off levels were prospectively evaluated to assess CD34+CD38−LSC levels at diagnosis (n = 594), and, to identify LSClow/LSChigh (n = 302) and MRDlow/MRDhigh patients (n = 305) in bone marrow in morphological complete remission (CR). In 242 CR patients combined MRD and LSC results were available. At diagnosis the CD34+CD38− LSC frequency independently predicts overall survival (OS). After achieving CR, combining LSC and MRD showed reduced survival in MRDhigh/LSChigh patients (hazard ratio [HR] 3.62 for OS and 5.89 for cumulative incidence of relapse [CIR]) compared to MRDlow/LSChigh, MRDhigh/LSClow, and especially MRDlow/LSClow patients. Moreover, in the NPM1mutant positive sub-group, prognostic value of golden standard NPM1-MRD by qPCR can be improved by addition of flow cytometric approaches. This is the first prospective study demonstrating that LSC strongly improves prognostic impact of MRD detection, identifying a patient subgroup with an almost 100% treatment failure probability, warranting consideration of LSC measurement incorporation in future AML risk schemes.
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