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Pediatric Adapted Risk index (PARI) to predict 2-year transplant related mortality post-HSCT in children.
Elfeky, Reem; Builes, Natalia; Pearce, Rachel M; Kania, Soumya P; Nademi, Zohreh; Lucchini, Giovanna; Chiesa, Robert; Amrolia, Persis J; Sorror, Mohamed L; Veys, Paul; Rao, Kanchan.
Afiliación
  • Elfeky R; 1. Immunology Department, Great Ormond Street Hospital, London, UK, United Kingdom.
  • Builes N; Hospital Pablo Tobon Uribe, Medellín, Colombia., medellin, Colombia.
  • Pearce RM; BSBMTCT data registry, London, United Kingdom.
  • Kania SP; UCL Great Ormond Street Institute of Child Health, University College London, London, UK, London, United Kingdom.
  • Nademi Z; Great North Children's Hospital, Newcastle upon Tyne, United Kingdom.
  • Lucchini G; 1. Blood and Bone marrow transplant Unit, Great Ormond Street Hospital, London, UK, United Kingdom.
  • Chiesa R; 1. Blood and Bone marrow transplant Unit, Great Ormond Street Hospital, London, UK, United Kingdom.
  • Amrolia PJ; 1. Blood and Bone marrow transplant Unit, Great Ormond Street Hospital, London, UK, United Kingdom.
  • Sorror ML; Fred Hutchinson Cancer Center and the University of Washington School of Medicine, Seattle, Washington, United States.
  • Veys P; Depts of Bone Marrow Transplantation, Great Ormond Street Hospital, London, Michigan, United Kingdom.
  • Rao K; 1. Blood and Bone marrow transplant Unit, Great Ormond Street Hospital, London, UK, United Kingdom.
Blood Adv ; 2024 Aug 02.
Article en En | MEDLINE | ID: mdl-39093984
ABSTRACT
Several attempts have been made to optimize pre-transplant risk assessment to improve hematopoietic stem cell transplantation (HSCT) decision-making and to predict outcome post- HSCT. However, its relevance to the pediatric population remains unclear. We report the results of revalidation of the HCT-CI in 874 children who received 944 HSCTs for malignant or non-malignant diseases at a single centre. After finding the HCT-CI invalid in our patient population; we proposed a modified pediatric adapted scoring system that captures risk factors (RF) and comorbidities (CoM) relevant to pediatrics. Each RF/CoM was assigned an integer weight based on its hazard ratio (HR) for TRM; 0 (HR <1.2), 1 (1.2 ≥HR <1.75), 2 (1.75 ≥HR <2.5), 3 (HR ≥2.5) .Using these weights, the pediatric adapted HSCT-RI (PARI) was devised, and patients were divided into 4 risk groups; group 1 without RF/CoM, group 2 scores 1-2, group 3 scores 3-4, group 4 scores ≥5. There was a linear increase in 2-year TRM from group 1 to 4 (TRM= 6.2% in group 1, 50.9% in group 4). PARI was successfully validated on an internal and external cohort of pediatric patients. Comparing models using c-statistics, PARI was found to be a better model than HCT-CI in predicting 2-year TRM in children with Akaike's and Schwarz's Bayesian information criteria (AIC and BIC) of 1069.245 and 1073.269; respectively using PARI vs 1223.158 and 1227.051; respectively using HCT-CI. We believe that PARI will be a valuable tool enabling better counselling and decision making for pediatric HSCT patients.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Blood Adv Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Blood Adv Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos