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Machine Learning Improves Risk Stratification in Myelofibrosis: An Analysis of the Spanish Registry of Myelofibrosis

Authors :
Mosquera Orgueira, Adrián
Pérez Encinas, Manuel
Hernández Sánchez, Alberto
González Martínez, Teresa
Arellano Rodrigo, Eduardo
Martínez Elicegui, Javier
Villaverde Ramiro, Ángela
Raya, José María
Ayala, Rosa
Ferrer Marín, Francisca
Fox, María Laura
Velez, Patricia
Mora, Elvira
Xicoy, Blanca
Mata Vázquez, María Isabel
García Fortes, María
Angona, Anna
Cuevas, Beatriz
Senín, María Alicia
Ramírez Payer, Angel
Ramírez, María José
Pérez López, Raúl
González de Villambrosía, Sonia
Martínez Valverde, Clara
Gómez Casares, María Teresa
García Hernández, Carmen
Gasior, Mercedes
Bellosillo Paricio, Beatriz
Steegmann, Juan Luis
Álvarez Larrán, Alberto
Hernández Rivas, Jesús María
Hernández Boluda, Juan Carlos
The Spanish MPN Group (GEMFIN).
Institut Català de la Salut
[Mosquera-Orgueira A, Pérez-Encinas M] Hospital Clínico Universitario, Santiago de Compostela, Spain. [Hernández-Sánchez A, González-Martínez T, Martínez-Elicegui J] Hospital Clínico, Salamanca, Spain. [Arellano-Rodrigo E] Hospital Clínic, Institut d’Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain. [Fox ML] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain
Vall d'Hebron Barcelona Hospital Campus
Source :
Scientia
Publication Year :
2023
Publisher :
Wolters Kluwer Health, 2023.

Abstract

Aprendizaje automático; Mielofibrosis Aprenentatge automàtic; Mielofibrosi Machine learning; Myelofibrosis Myelofibrosis (MF) is a myeloproliferative neoplasm (MPN) with heterogeneous clinical course. Allogeneic hematopoietic cell transplantation remains the only curative therapy, but its morbidity and mortality require careful candidate selection. Therefore, accurate disease risk prognostication is critical for treatment decision-making. We obtained registry data from patients diagnosed with MF in 60 Spanish institutions (N = 1386). These were randomly divided into a training set (80%) and a test set (20%). A machine learning (ML) technique (random forest) was used to model overall survival (OS) and leukemia-free survival (LFS) in the training set, and the results were validated in the test set. We derived the AIPSS-MF (Artificial Intelligence Prognostic Scoring System for Myelofibrosis) model, which was based on 8 clinical variables at diagnosis and achieved high accuracy in predicting OS (training set c-index, 0.750; test set c-index, 0.744) and LFS (training set c-index, 0.697; test set c-index, 0.703). No improvement was obtained with the inclusion of MPN driver mutations in the model. We were unable to adequately assess the potential benefit of including adverse cytogenetics or high-risk mutations due to the lack of these data in many patients. AIPSS-MF was superior to the IPSS regardless of MF subtype and age range and outperformed the MYSEC-PM in patients with secondary MF. In conclusion, we have developed a prediction model based exclusively on clinical variables that provides individualized prognostic estimates in patients with primary and secondary MF. The use of AIPSS-MF in combination with predictive models that incorporate genetic information may improve disease risk stratification.

Details

Language :
English
Database :
OpenAIRE
Journal :
Scientia
Accession number :
edsair.doi.dedup.....c51c89b150fbc1df5a63c53faab62cc1