CD34+CD38− leukemic stem cell frequency to predict outcome in acute myeloid leukemia

被引:0
作者
Wendelien Zeijlemaker
Tim Grob
Rosa Meijer
Diana Hanekamp
Angèle Kelder
Jannemieke C. Carbaat-Ham
Yvonne J. M. Oussoren-Brockhoff
Alexander N. Snel
Dennis Veldhuizen
Willemijn J. Scholten
Johan Maertens
Dimitri A. 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
Peter J. M. Valk
Mojca Jongen-Lavrencic
Gert J. Ossenkoppele
Gerrit J. Schuurhuis
机构
[1] VU University Medical Center,Department of Hematology
[2] Cancer Center Amsterdam,Department of Hematology
[3] Erasmus University Medical Center,Clinical trial Center
[4] Erasmus University Medical Center, HOVON data center
[5] University Hospitals Leuven,Department of Hematology
[6] Campus Gasthuisberg,Department of Hematology
[7] Ziekenhuis Netwerk Antwerpen,Department of Hematology
[8] Inselspital,Department of Hematology
[9] Bern University Hospital,Department of Immunology, Erasmus MC
[10] University and University Hospital Zürich,Department of Clinical Chemistry
[11] University Medical Center Rotterdam,Department of Laboratory Medicine – Laboratory for Hematology
[12] Medisch Spectrum Twente/Medlon,Department of Pediatric Oncology/Hematology
[13] Radboud University Nijmegen Medical Center,undefined
[14] RUNMC,undefined
[15] VU University Medical Center,undefined
来源
Leukemia | 2019年 / 33卷
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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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页码:1102 / 1112
页数:10
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