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An artificial intelligence-driven predictive model for pediatric allogeneic hematopoietic stem cell transplantation using clinical variables.
Echecopar, Carlos; Abad, Inés; Galán-Gómez, Víctor; Mozo Del Castillo, Yasmina; Sisinni, Luisa; Bueno, David; Ruz, Beatriz; Pérez-Martínez, Antonio.
Afiliação
  • Echecopar C; Pediatric Hemato-Oncology, La Paz University Hospital, Madrid, Spain.
  • Abad I; Pediatric Department, Autonomous University of Madrid, Madrid, Spain.
  • Galán-Gómez V; Pediatric Hemato-Oncology, La Paz University Hospital, idiPAZ Research Institute, Madrid, Spain.
  • Mozo Del Castillo Y; Pediatric Hemato-Oncology, La Paz University Hospital, idiPAZ Research Institute, Madrid, Spain.
  • Sisinni L; Pediatric Hemato-Oncology, La Paz University Hospital, idiPAZ Research Institute, Madrid, Spain.
  • Bueno D; Pediatric Hemato-Oncology, La Paz University Hospital, idiPAZ Research Institute, Madrid, Spain.
  • Ruz B; Institute of Medical and Molecular Genetics (INGEMM) idiPAZ Research Institute, La Paz University Hospital, Madrid, Spain.
  • Pérez-Martínez A; Pediatric Hemato-Oncology, La Paz University Hospital, Madrid, Spain.
Eur J Haematol ; 112(6): 910-916, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38333914
ABSTRACT

BACKGROUND:

Hematopoietic stem cell transplantation (HSCT) is a procedure with high morbidity and mortality. Identifying patients for maximum benefit and risk assessment is crucial in the decision-making process. This has led to the development of predictive risk models for HSCT in adults, which have limitations when applied to pediatric population. Our goal was to develop an automatic learning algorithm to predict survival in children with malignant disorders undergoing HSCT.

METHODS:

We studied allogenic HSCTs performed on children with malignant disorders at a third-level hospital between 1991 and 2021. Survival was analyzed using the Kaplan-Meier method, log-rank test for the univariate analysis, and Cox regression for the multivariate analysis. A prognostic index was constructed based on these findings. Lastly, we constructed a predictive model using a random forest algorithm to forecast 1-year survival after HSCT.

RESULTS:

We analyzed 229 HSCTs in 201 patients with a median follow-up of 1.64 years. Variables that impacted on the multivariate analysis were older age (hazard ratio [HR] 1.40, 95% confidence interval [CI] 1.12-1.76, p = .003), oldest period of HSCT (HR 0.46, 95% CI 0.29-0.73, p < .001), and mismatched donor (HR 2.65, 95% CI 1.51-4.65, p = .001). Our prognostic index was associated with 3-year overall survival (OS; p < .001). A random forest was developed using as variables diagnosis, age, year of HSCT, time from diagnosis to HSCT, disease stage, donor type, and conditioning. This achieved 72% accuracy in predicting 1-year OS.

CONCLUSIONS:

Our index and random forest was effective in predicting 1-year survival. However, further validation in diverse populations is necessary to establish their generalizability.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante Homólogo / Inteligência Artificial / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Eur J Haematol Assunto da revista: HEMATOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante Homólogo / Inteligência Artificial / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Eur J Haematol Assunto da revista: HEMATOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Espanha
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