Conditioning intensity and peritransplant flow cytometric MRD dynamics in adult AML

  • Gabrielle Paras
    Department of Medicine, Residency Program, University of Washington, Seattle, WA;
  • Linde M. Morsink
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Megan Othus
    Public Health Science Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Filippo Milano
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Brenda M. Sandmaier
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Lucas C. Zarling
    Department of Medicine, Residency Program, University of Washington, Seattle, WA;
  • Raffaele Palmieri
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Gary Schoch
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Chris Davis
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Marie Bleakley
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Mary E. D. Flowers
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • H. Joachim Deeg
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Frederick R. Appelbaum
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Rainer Storb
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Roland B. Walter
    Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;

抄録

<jats:title>Abstract</jats:title><jats:p>In acute myeloid leukemia (AML), measurable residual disease (MRD) before or after allogeneic hematopoietic cell transplantation (HCT) is an established independent indicator of poor outcome. To address how peri-HCT MRD dynamics could refine risk assessment across different conditioning intensities, we analyzed 810 adults transplanted in first or second remission after myeloablative conditioning (MAC; n = 515) or non-MAC (n = 295) who underwent multiparameter flow cytometry–based MRD testing before as well as 20 to 40 days after allografting. Patients without pre- and post-HCT MRD (MRDneg/MRDneg) had the lowest risks of relapse and highest relapse-free survival (RFS) and overall survival (OS). Relative to those patients, outcomes for MRDpos/MRDpos and MRDneg/MRDpos patients were poor regardless of conditioning intensity. Outcomes for MRDpos/MRDneg patients were intermediate. Among 161 patients with MRD before HCT, MRD was cleared more commonly with a MAC (85 of 104; 81.7%) than non-MAC (33 of 57; 57.9%) regimen (P = .002). Although non-MAC regimens were less likely to clear MRD, if they did, the impact on outcome was greater. Thus, there was a significant interaction between conditioning intensity and “MRD conversion” for relapse (P = .020), RFS (P = .002), and OS (P = .001). Similar findings were obtained in the subset of 590 patients receiving HLA-matched allografts. C-statistic values were higher (indicating higher predictive accuracy) for peri-HCT MRD dynamics compared with the isolated use of pre-HCT MRD status or post-HCT MRD status for prediction of relapse, RFS, and OS. Across conditioning intensities, peri-HCT MRD dynamics improve risk assessment over isolated pre- or post-HCT MRD assessments in patients with AML.</jats:p>

収録刊行物

  • Blood

    Blood 139 (11), 1694-1706, 2022-03-17

    American Society of Hematology

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