Multicolor flow cytometry and multigene next-generation sequencing are complementary and highly predictive for relapse in acute myeloid leukemia after allogeneic transplantation Journal Article


Authors: Getta, B. M.; Devlin, S. M.; Levine, R. L.; Arcila, M. E.; Mohanty, A. S.; Zehir, A.; Tallman, M. S.; Giralt, S. A.; Roshal, M.
Article Title: Multicolor flow cytometry and multigene next-generation sequencing are complementary and highly predictive for relapse in acute myeloid leukemia after allogeneic transplantation
Abstract: Minimal residual disease (MRD) in acute myeloid leukemia (AML) is typically measured using multiparameter flow cytometry (MFC). Detection of leukemia mutations using multigene next-generation sequencing (NGS) can potentially be used to measure residual disease. We used a targeted 28-gene NGS panel to detect mutations and different-from-normal 10-color MFC to measure MRD in AML patients before allogeneic hematopoietic stem cell transplantation (HCT). Residual disease was defined when any abnormal blast population was detected using MFC and when any leukemia allele was detected with a variant allele frequency (VAF) ≥ 5% using NGS. We tracked the clearance of leukemia alleles between AML diagnosis and immediately before HCT and found that mutations in DNMT3A, TET2, and JAK2 were less likely to be cleared than NPM1, IDH 1/2, and FLT3-ITD. Despite varying sensitivities, the concordance rate of residual disease detection before HCT using the 2 assays was 44 of 62 (71%) evaluable cases. Discordance could be explained by residual mutations in DNMT3A and TET2 that were not detected by MFC and presence of residual leukemia mutations with VAF below the established thresholds for mutation calling. Presence of flow MRD and residual mutations immediately before HCT using the 2 assays was associated with relapse risk (MFC: hazard ratio, 4.62; 95% confidence interval [CI], 1.32 to 16.09; P =.016 and NGS: hazard ratio, 4.35; 95% CI, 1.63 to 11.6; P =.003) and survival (MFC: hazard ratio, 2.44; 95% CI, 1 to 5.97; P =.05 and NGS: hazard ratio, 2.1; 95% CI,.97 to 4.55; P =.059) after HCT. Residual disease detected concurrently by MFC and NGS conferred the highest relapse risk compared with patients who were either negative by both assays or had discordant status (overall, P =.008). Although MFC is universally applicable, a multigene NGS approach to measuring residual disease in AML provides additional information on differential clearance of disease alleles and can assess clonal architecture before transplantation. © 2017 The American Society for Blood and Marrow Transplantation
Keywords: flow cytometry; minimal residual disease; acute myeloid leukemia; next-generation sequencing
Journal Title: Biology of Blood and Marrow Transplantation
Volume: 23
Issue: 7
ISSN: 1083-8791
Publisher: Elsevier Inc.  
Date Published: 2017-07-01
Start Page: 1064
End Page: 1071
Language: English
DOI: 10.1016/j.bbmt.2017.03.017
PROVIDER: scopus
PUBMED: 28315400
DOI/URL:
Notes: Article -- Export Date: 3 July 2017 -- Source: Scopus
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MSK Authors
  1. Sergio Andres Giralt
    1066 Giralt
  2. Martin Stuart Tallman
    653 Tallman
  3. Ross Levine
    785 Levine
  4. Ahmet Zehir
    345 Zehir
  5. Maria Eugenia Arcila
    669 Arcila
  6. Sean McCarthy Devlin
    614 Devlin
  7. Mikhail Roshal
    236 Roshal
  8. Abhinita Subhadarshin Mohanty
    39 Mohanty
  9. Bartlomiej Marcin Getta
    29 Getta