TY - JOUR
T1 - Impact of measurable residual disease by decentralized flow cytometry
T2 - a PETHEMA real-world study in 1076 patients with acute myeloid leukemia
AU - PETHEMA (Programa para el Estudio de la Terapéutica en Hemopatías Malignas) cooperative study group
AU - Paiva, Bruno
AU - Vidriales, María Belen
AU - Sempere, Amparo
AU - Tarín, Fabián
AU - Colado, Enrique
AU - Benavente, Celina
AU - Cedena, María Teresa
AU - Sánchez, Joaquín
AU - Caballero-Velazquez, Teresa
AU - Cordón, Lourdes
AU - Garces, Juan Jose
AU - Simoes, Catia
AU - Martínez-Cuadrón, David
AU - Bernal, Teresa
AU - Botella, Carmen
AU - Grille, Sofia
AU - Serrano, Josefina
AU - Rodríguez-Medina, Carlos
AU - Algarra, Lorenzo
AU - Alonso-Domínguez, Juan Manuel
AU - Amigo, María Luz
AU - Barrios, Manuel
AU - García-Boyero, Raimundo
AU - Colorado, Mercedes
AU - Pérez-Oteyza, Jaime
AU - Pérez-Encinas, Manuel
AU - Costilla-Barriga, Lisette
AU - Sayas, María José
AU - Pérez, Olga
AU - González-Díaz, Marcos
AU - Pérez-Simón, José A.
AU - Martínez-López, Joaquín
AU - Sossa, Claudia
AU - Orfao, Alberto
AU - San Miguel, Jesús F.
AU - Sanz, Miguel Ángel
AU - Montesinos, Pau
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2021/8
Y1 - 2021/8
N2 - The role of decentralized assessment of measurable residual disease (MRD) for risk stratification in acute myeloid leukemia (AML) remains largely unknown, and so it does which methodological aspects are critical to empower the evaluation of MRD with prognostic significance, particularly if using multiparameter flow cytometry (MFC). We analyzed 1076 AML patients in first remission after induction chemotherapy, in whom MRD was evaluated by MFC in local laboratories of 60 Hospitals participating in the PETHEMA registry. We also conducted a survey on technical aspects of MRD testing to determine the impact of methodological heterogeneity in the prognostic value of MFC. Our results confirmed the recommended cutoff of 0.1% to discriminate patients with significantly different cumulative-incidence of relapse (-CIR- HR:0.71, P < 0.001) and overall survival (HR: 0.73, P = 0.001), but uncovered the limited prognostic value of MFC based MRD in multivariate and recursive partitioning models including other clinical, genetic and treatment related factors. Virtually all aspects related with methodological, interpretation, and reporting of MFC based MRD testing impacted in its ability to discriminate patients with different CIR. Thus, this study demonstrated that “real-world” assessment of MRD using MFC is prognostic in patients at first remission, and urges greater standardization for improved risk-stratification toward clinical decisions in AML.
AB - The role of decentralized assessment of measurable residual disease (MRD) for risk stratification in acute myeloid leukemia (AML) remains largely unknown, and so it does which methodological aspects are critical to empower the evaluation of MRD with prognostic significance, particularly if using multiparameter flow cytometry (MFC). We analyzed 1076 AML patients in first remission after induction chemotherapy, in whom MRD was evaluated by MFC in local laboratories of 60 Hospitals participating in the PETHEMA registry. We also conducted a survey on technical aspects of MRD testing to determine the impact of methodological heterogeneity in the prognostic value of MFC. Our results confirmed the recommended cutoff of 0.1% to discriminate patients with significantly different cumulative-incidence of relapse (-CIR- HR:0.71, P < 0.001) and overall survival (HR: 0.73, P = 0.001), but uncovered the limited prognostic value of MFC based MRD in multivariate and recursive partitioning models including other clinical, genetic and treatment related factors. Virtually all aspects related with methodological, interpretation, and reporting of MFC based MRD testing impacted in its ability to discriminate patients with different CIR. Thus, this study demonstrated that “real-world” assessment of MRD using MFC is prognostic in patients at first remission, and urges greater standardization for improved risk-stratification toward clinical decisions in AML.
UR - http://www.scopus.com/inward/record.url?scp=85100095112&partnerID=8YFLogxK
U2 - 10.1038/s41375-021-01126-3
DO - 10.1038/s41375-021-01126-3
M3 - Artículo Científico
C2 - 33526859
AN - SCOPUS:85100095112
SN - 0887-6924
VL - 35
SP - 2358
EP - 2370
JO - Leukemia
JF - Leukemia
IS - 8
ER -