主页 文献库文献详情
PMID: 42574467 已发表 · epublish 英语

Multicenter Flow Cytometry For Acute Myeloid Leukemia Measurable Residual Disease With LAIP/DfN And CD34+CD38- Leukemic Stem Cell-Enriched Populations.

Journal of visualized experiments : JoVE ·第 233 期 ·2026-07-21

Plesa A, Dumezy F, Mathis S, Arnoux I, Saada V, Bardet V, Oster I, Badaoui B, Bera E, Bonneville E, Bouslama B, Chapuis N, Chauvel C, Cornet E, Dannus LT, Debord C, Feger F, Feuillard J, Fournet T, Garnache F, Geneviève F, Gerard D, Monteiro VG, Guy J, Harrivel V, Hemar C, Jadeau C, Mayeur-Rousse C, Lapillonne H, Latger-Cannard V, Garff-Tavernier ML, Lemaire P, Letestu R, Lhoumeau AC, Manzoni D, Mimoun A, Nivaggioni V, Osman J, Raggueneau V, Rambaud H, Raskovalova T, Roggy A, Roussel M, Sciortino D, Soenen V, Vergez F, Masson RV, Vial JP, Vogrig M, Wagner-Ballon O, Zhu J, Celli-Lebras K, Itzykson R, Recher C, Dombret H, Preudhomme C, Roumier C

摘要

Measurable residual disease (MRD) follow-up is recommended for treatment response evaluation in acute myeloid leukemia (AML) clinical trials according to ELN 2025 guidelines. The aim of this study was to implement a standardized follow-up of patients using a harmonized MRD flow approach across 30 French hematology laboratories participating in AML clinical trials. To obtain comparable results, the network established recommendations from wet-lab procedures to clinical reports. We designed a 3-tube panel with mandatory 8-color common markers per tube, according to ELN recommendations, to identify leukemia-associated immunophenotype/different-from-normal (LAIP/DfN) patterns in bulk cells and leukemic stem cell (LSC)-enriched populations in the CD34+CD38- fraction. A backbone of CD34/CD38/CD45/CD117 was used, completed by lineage markers for the first tube, LSC-associated markers for the second tube, and monocytic and differentiation markers for the third tube. This panel can be used in 8-, 10-, and 12-color formats and implemented on multiple conventional flow cytometer platforms. We propose flow cytometer settings adapted to each platform. Harmonization of sensitivity between the four platforms was performed using 8-peak rainbow beads. Immunostaining was performed after bulk lysis. To detect bias between platforms, the staining index was tested using fresh healthy bone marrow samples in parallel on the four platforms. Regular bone marrow quality-control samples were shared among laboratories for wet external quality assessment (EQA) to verify all steps of the protocol. Finally, standardization of the data analysis strategy obtained in the centers was evaluated using dry EQA by sharing MRD FCS data files. The feasibility of this multicenter approach requires harmonization of instrument sensitivity and sample preparation, as well as training and systematic education of analytical operators.

文献信息
期刊
Journal of visualized experiments : JoVE
期刊简称
J Vis Exp
ISSN
1940-087X
发表日期
2026-07-21
语言
英语
国家/地区
United States
NLM ID
101313252
分析服务
分析服务

联系地址

山东省济南市章丘区文博路2号

齐鲁师范学院 genelibs生信实验室

山东省济南市高新区舜华路750号

大学科技园北区F座4单元2楼

电话: 0531-88819269

微信公众号

关注微信订阅号,实时查看信息,关注医学生物学动态。


商务邮箱

E-mail: [email protected]