TY - JOUR
T1 - Machine Learning Improves Risk Stratification in Myelofibrosis :
T2 - An Analysis of the Spanish Registry of Myelofibrosis
AU - Mosquera-Orgueira, Adrián
AU - Pérez-Encinas, Manuel
AU - Hernández-Sánchez, Alberto
AU - González-Martínez, Teresa
AU - Arellano-Rodrigo, Eduardo
AU - Martínez-Elicegui, Javier
AU - Villaverde-Ramiro, Ángela
AU - Raya, José-María
AU - Ayala, Rosa
AU - Ferrer-Marín, Francisca
AU - Fox, Maria Laura
AU - Velez, Patricia
AU - Mora, Elvira
AU - Xicoy, Blanca
AU - Mata-Vázquez, María-Isabel
AU - García Fortes, María
AU - Angona, Anna
AU - Cuevas, Beatriz
AU - Senín, María-Alicia
AU - Ramírez-Payer, Angel
AU - Ramírez, María-José
AU - Pérez-López, Raúl
AU - González de Villambrosía, Sonia
AU - Martínez-Valverde, Clara
AU - Gómez-Casares, María-Teresa
AU - García-Hernández, Carmen
AU - Gasior, Mercedes
AU - Bellosillo Paricio, Beatriz
AU - Steegmann, Juan-Luis
AU - Álvarez-Larrán, Alberto
AU - Hernández Rivas, Jesús María
AU - Hernandez-Boluda, Juan Carlos
PY - 2022
Y1 - 2022
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/85144962893
U2 - 10.1097/HS9.0000000000000818
DO - 10.1097/HS9.0000000000000818
M3 - Article
C2 - 36570691
SN - 2572-9241
VL - 7
JO - HemaSphere
JF - HemaSphere
ER -