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Machine Learning Improves Risk Stratification in Myelodysplastic Neoplasms: An Analysis of the Spanish Group of Myelodysplastic Syndromes.
Mosquera Orgueira, Adrian; Perez Encinas, Manuel Mateo; Diaz Varela, Nicolas A; Mora, Elvira; Díaz-Beyá, Marina; Montoro, María Julia; Pomares, Helena; Ramos, Fernando; Tormo, Mar; Jerez, Andres; Nomdedeu, Josep F; De Miguel Sanchez, Carlos; Leonor, Arenillas; Cárcel, Paula; Cedena Romero, Maria Teresa; Xicoy, Blanca; Rivero, Eugenia; Del Orbe Barreto, Rafael Andres; Diez-Campelo, Maria; Benlloch, Luis E; Crucitti, Davide; Valcárcel, David.
Afiliação
  • Mosquera Orgueira A; Complexo Hospitalario Universitario de Santiago de Compostela, Department of Hematology, Instituto de Investigacións Sanitarias de Santiago, Santiago de Compostela, Spain.
  • Perez Encinas MM; Complexo Hospitalario Universitario de Santiago de Compostela, Department of Hematology, Instituto de Investigacións Sanitarias de Santiago, Santiago de Compostela, Spain.
  • Diaz Varela NA; Hospital Central de Asturias, Oviedo, Spain.
  • Mora E; Hematology Department, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
  • Díaz-Beyá M; Hospital Clinic, Dept. of Hematology, IDIBAPS, Barcelona, Spain.
  • Montoro MJ; Department of Hematology, Vall d'Hebron Institute of Oncology (VHIO), Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • Pomares H; Hematology Department., Hospital Duran i Reynals. Institut Català d'Oncologia, Hospital Duran i Reynals. Institut Català d'Oncologia, Hospitalet, Barcelona, Spain.
  • Ramos F; Department of Hematology, Hospital Universitario de León, Spain.
  • Tormo M; Servicio de Hematología. Hospital Clínico Universitario de Valencia, Spain.
  • Jerez A; Hematology and Medical Oncology Department, Hospital Morales Meseguer, IMIB, Murcia, Spain.
  • Nomdedeu JF; Hematology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • De Miguel Sanchez C; Hospital Universitario de Álava - Sede Txagorritxu, Vitoria-Gasteiz, Spain.
  • Leonor A; Laboratoris de Citologia Hematològica i Citogenètica, servei de Patologia, Hospital del Mar. GRETNHE- Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain.
  • Cárcel P; Department of Hematology, Hospital Público Universitario de la Ribera, Alzira, Valencia, Spain.
  • Cedena Romero MT; Hospital Universitario 12 de Octubre, Instituto de Investigación Sanitaria i+12, Madrid, Spain.
  • Xicoy B; HU German Trias i Pujol - Institut Català d' Oncologia, Josep Carreras Leukemia Research Institute, Universitat Autònoma de Barcelona, Badalona, Spain.
  • Rivero E; Department of Hematology, University Hospital Arnau de Vilanova, Lleida, Spain.
  • Del Orbe Barreto RA; Edif. Laboratorios, planta baja., Hospital Universitario Cruces Servicio de Hematología. Sección Eritropatología - Hem. Molecular, Barakaldo, Spain.
  • Diez-Campelo M; Hematology Department, Institute of Biomedical Research of Salamanca, University Hospital of Salamanca, Spain.
  • Benlloch LE; Grupo Español de Síndromes Mielodisplásicos (GESMD), Valencia, Spain.
  • Crucitti D; Instituto de Investigacions Sanitarias de Santiago de Compostela (IDIS-CHUS), Santiago de Compostela, Spain.
  • Valcárcel D; Department of Hematology, Vall d'Hebron Institute of Oncology (VHIO), Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Hemasphere ; 7(10): e961, 2023 Oct.
Article em En | MEDLINE | ID: mdl-37841754
ABSTRACT
Myelodysplastic neoplasms (MDS) are a heterogeneous group of hematological stem cell disorders characterized by dysplasia, cytopenias, and increased risk of acute leukemia. As prognosis differs widely between patients, and treatment options vary from observation to allogeneic stem cell transplantation, accurate and precise disease risk prognostication is critical for decision making. With this aim, we retrieved registry data from MDS patients from 90 Spanish institutions. A total of 7202 patients were included, which were divided into a training (80%) and a test (20%) set. A machine learning technique (random survival forests) was used to model overall survival (OS) and leukemia-free survival (LFS). The optimal model was based on 8 variables (age, gender, hemoglobin, leukocyte count, platelet count, neutrophil percentage, bone marrow blast, and cytogenetic risk group). This model achieved high accuracy in predicting OS (c-indexes; 0.759 and 0.776) and LFS (c-indexes; 0.812 and 0.845). Importantly, the model was superior to the revised International Prognostic Scoring System (IPSS-R) and the age-adjusted IPSS-R. This difference persisted in different age ranges and in all evaluated disease subgroups. Finally, we validated our results in an external cohort, confirming the superiority of the Artificial Intelligence Prognostic Scoring System for MDS (AIPSS-MDS) over the IPSS-R, and achieving a similar performance as the molecular IPSS. In conclusion, the AIPSS-MDS score is a new prognostic model based exclusively on traditional clinical, hematological, and cytogenetic variables. AIPSS-MDS has a high prognostic accuracy in predicting survival in MDS patients, outperforming other well-established risk-scoring systems.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article