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Prognostic Value of Measurable Residual Disease in Patients with AML Undergoing HSCT: A Multicenter Study

Authors :
Teresa Caballero-Velázquez
Olga Pérez-López
Ana Yeguas Bermejo
Eduardo Rodríguez Arbolí
Enrique Colado Varela
Amparo Sempere Talens
María Belén Vidriales
María Solé-Rodríguez
Covadonga Quirós Caso
Estefanía Pérez López
Marta Reinoso Segura
Concepción Prats-Martín
Pau Montesinos
Jose A. Pérez-Simón
Source :
Cancers; Volume 15; Issue 5; Pages: 1609
Publication Year :
2023
Publisher :
MDPI AG, 2023.

Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) represents the best therapeutic option for many patients with acute myeloid leukemia (AML). However, relapse remains the main cause of mortality after transplantation. The detection of measurable residual disease (MRD) by multiparameter flow cytometry (MFC) in AML, before and after HSCT, has been described as a powerful predictor of outcome. Nevertheless, multicenter and standardized studies are lacking. A retrospective analysis was performed, including 295 AML patients undergoing HSCT in 4 centers that worked according to recommendations from the Euroflow consortium. Among patients in complete remission (CR), MRD levels prior to transplantation significantly influenced outcomes, with overall (OS) and leukemia free survival (LFS) at 2 years of 76.7% and 67.6% for MRD-negative patients, 68.5% and 49.7% for MRD-low patients (MRD < 0.1), and 50.5% and 36.6% for MRD-high patients (MRD ≥ 0.1) (p < 0.001), respectively. MRD level did influence the outcome, irrespective of the conditioning regimen. In our patient cohort, positive MRD on day +100 after transplantation was associated with an extremely poor prognosis, with a cumulative incidence of relapse of 93.3%. In conclusion, our multicenter study confirms the prognostic value of MRD performed in accordance with standardized recommendations.

Details

ISSN :
20726694
Volume :
15
Database :
OpenAIRE
Journal :
Cancers
Accession number :
edsair.doi.dedup.....1da7cd94e274a306f37768df311ddca6
Full Text :
https://doi.org/10.3390/cancers15051609