Technical and Clinical Validity of Assessing Measurable Residual Disease by Multicolor Flow Cytometry in an Unselected Acute Myeloid Leukemia Patient Cohort.

* Context.--Following the validation of a multicolor flow cytometry (MFC) assay for measurable residual disease (MRD) in acute myeloid leukemia (AML), this study examines its clinical applicability. Objective.--To evaluate the practicality and performance of MFC-based MRD detection in AML. Design.--...

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Publicado en:Archives of Pathology & Laboratory Medicine Vol. 150; no. 1; pp. 72 - 81
Autores principales: Wang, Sa A., Li, Shaoying, Wang, Wei, Xu, Jie, Thakral, Beenu, Hu, Shimin, Ok, Chi Young, Jia, Fuli, Jorgensen, Jeffrey L., Medeiros, L. Jeffrey, Ravandi, Farhad, Short, Nicholas J., Loghavi, Sanam
Formato: research tables/charts Journal Article
Publicado: College of American Pathologists Jan2026
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jan2026
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      pub: College of American Pathologists
      place: Northfield, Illinois
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        10.5858/arpa.2025-0053-OA
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        atl: Technical and Clinical Validity of Assessing Measurable Residual Disease by Multicolor Flow Cytometry in an Unselected Acute Myeloid Leukemia Patient Cohort.
      aug:
        au:
          Wang, Sa A.
          Li, Shaoying
          Wang, Wei
          Xu, Jie
          Thakral, Beenu
          Hu, Shimin
          Ok, Chi Young
          Jia, Fuli
          Jorgensen, Jeffrey L.
          Medeiros, L. Jeffrey
          Ravandi, Farhad
          Short, Nicholas J.
          Loghavi, Sanam
        affil: Department of Hematopathology, University of Texas MD Anderson Cancer Center, Houston
      sug:
        subj:
          Leukemia, Myeloid, Acute Prognosis
          Neoplasm Recurrence, Local Risk Factors
          Disease Remission Diagnosis
          Flow Cytometry Methods
          Instrument Validation
          Risk Assessment
          Human
          Middle Age
          Aged
          Aged, 80 and Over
          Male
          Female
          Validation Studies
          Prospective Studies
          Genetics
          Survival Analysis
          Bone Marrow Examination
          Descriptive Statistics
          Hematopoiesis
          Disease-Free Survival
          Overall Survival
          False Negative Results
          Sequence Analysis
          Reverse Transcriptase Polymerase Chain Reaction
          Fisher's Exact Test
          T-Tests
          Comparative Studies
          Kaplan-Meier Estimator
          Data Analysis Software
          Middle Aged: 45-64 years
          Aged: 65+ years
          Aged, 80 & over
          Male
          Female
      ab: * Context.--Following the validation of a multicolor flow cytometry (MFC) assay for measurable residual disease (MRD) in acute myeloid leukemia (AML), this study examines its clinical applicability. Objective.--To evaluate the practicality and performance of MFC-based MRD detection in AML. Design.--Prospectively assessed AML MRD MFC in unselected AML patients achieving morphologic remission with follow-up studies, molecular genetics, and survival data. Results.--Among 379 patient bone marrow samples in this cohort, an interpretable result was obtained in 359 (95%). A total of 57 of the 359 cases (16%) were positive for MRD, and the most frequently observed immunophenotype was CD34-/CD117+ myeloid (n = 46; 81%), followed by CD34-/CD117+ myeloid (n = 8; 14%) and monocytic (n = 3; 5%). Of 57 MRD1 cases, 6 (11%) had no leukemia-associated immunophenotypes available, and 16 of 51 (31%) with leukemia- associated immunophenotype for comparison exhibited significant immunophenotypic drift/switch, highlighting the importance of the "deviation from normal" approach. The remaining 302 cases were MRD negative; among these, 21 (7%) displayed a preleukemic immunophenotype that was associated with persistent clonal hematopoiesis in 18 patients (86%). A positive MFC result was strongly associated with subsequent follow-up positive MRD (41 of 45 [91%] versus 14 of 240 [6%], P < .01), morphologic relapse (42 of 55 [76%] versus 48 of 301 [16%], P < .01), an inferior overall survival (12.5 months versus not reached, P < .01), and leukemia-free survival (6.5 months versus not reached, P < .01). Among MRD-negative patients, a preleukemic phenotype was associated with a shorter overall survival (P = .03), but not leukemia-free survival (P = .16). Conclusions.--Our study provides data-driven technical insights for laboratories considering MFC AML MRD implementation and offers strong evidence supporting the utility of MRD assessment by MFC in patients with AML undergoing various stages of treatment and surveillance.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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