Conditioning intensity and peritransplant flow cytometric MRD dynamics in adult AML.


Journal

Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509

Informations de publication

Date de publication:
17 03 2022
Historique:
received: 12 11 2021
accepted: 28 12 2021
pubmed: 8 1 2022
medline: 5 4 2022
entrez: 7 1 2022
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 34995355
pii: S0006-4971(22)00035-0
doi: 10.1182/blood.2021014804
pmc: PMC8931514
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1694-1706

Subventions

Organisme : NCI NIH HHS
ID : P01 CA018029
Pays : United States
Organisme : NCI NIH HHS
ID : P01 CA078902
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA015704
Pays : United States

Informations de copyright

© 2022 by The American Society of Hematology.

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Auteurs

Gabrielle Paras (G)

Department of Medicine, Residency Program, University of Washington, Seattle, WA.

Linde M Morsink (LM)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Department of Hematology, University Medical Center Groningen, Groningen, The Netherlands.

Megan Othus (M)

Public Health Science Division, Fred Hutchinson Cancer Research Center, Seattle, WA.

Filippo Milano (F)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Division of Medical Oncology, Department of Medicine, University of Washington, Seattle, WA.

Brenda M Sandmaier (BM)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Division of Medical Oncology, Department of Medicine, University of Washington, Seattle, WA.

Lucas C Zarling (LC)

Department of Medicine, Residency Program, University of Washington, Seattle, WA.

Raffaele Palmieri (R)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Hematology, University Tor Vergata, Rome, Italy; and.

Gary Schoch (G)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.

Chris Davis (C)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.

Marie Bleakley (M)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Department of Pediatrics.

Mary E D Flowers (MED)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Division of Medical Oncology, Department of Medicine, University of Washington, Seattle, WA.

H Joachim Deeg (HJ)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Division of Medical Oncology, Department of Medicine, University of Washington, Seattle, WA.

Frederick R Appelbaum (FR)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Division of Medical Oncology, Department of Medicine, University of Washington, Seattle, WA.

Rainer Storb (R)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Division of Medical Oncology, Department of Medicine, University of Washington, Seattle, WA.

Roland B Walter (RB)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Division of Hematology, Department of Medicine.
Department of Laboratory Medicine & Pathology, and.
Department of Epidemiology, University of Washington, Seattle, WA.

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