A validated pediatric disease risk index for allogeneic hematopoietic cell transplantation.
Adolescent
Age Factors
Allografts
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Child
Child, Preschool
Cohort Studies
Combined Modality Therapy
Disease-Free Survival
Female
Hematopoietic Stem Cell Transplantation
Humans
Infant
Kaplan-Meier Estimate
Leukemia, Myeloid, Acute
/ drug therapy
Male
Neoplasm, Residual
Precursor Cell Lymphoblastic Leukemia-Lymphoma
/ drug therapy
Prognosis
Random Allocation
Risk Assessment
Risk Factors
Severity of Illness Index
Journal
Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509
Informations de publication
Date de publication:
18 02 2021
18 02 2021
Historique:
received:
28
09
2020
accepted:
04
11
2020
pubmed:
19
11
2020
medline:
3
7
2021
entrez:
18
11
2020
Statut:
ppublish
Résumé
A disease risk index (DRI) that was developed for adults with hematologic malignancy who were undergoing hematopoietic cell transplantation is also being used to stratify children and adolescents by disease risk. Therefore, to develop and validate a DRI that can be used to stratify those with AML and ALL by their disease risk, we analyzed 2569 patients aged <18 years with acute myeloid (AML; n = 1224) or lymphoblastic (ALL; n = 1345) leukemia who underwent hematopoietic cell transplantation. Training and validation subsets for each disease were generated randomly with 1:1 assignment to the subsets, and separate prognostic models were derived for each disease. For AML, 4 risk groups were identified based on age, cytogenetic risk, and disease status, including minimal residual disease status at transplantation. The 5-year leukemia-free survival for low (0 points), intermediate (2, 3, 5), high (7, 8), and very high (>8) risk groups was 78%, 53%, 40%, and 25%, respectively (P < .0001). For ALL, 3 risk groups were identified based on age and disease status, including minimal residual disease status at transplantation. The 5-year leukemia-free survival for low (0 points), intermediate (2-4), and high (≥5) risk groups was 68%, 51%, and 33%, respectively (P < .0001). We confirmed that the risk groups could be applied to overall survival, with 5-year survival ranging from 80% to 33% and 73% to 42% for AML and ALL, respectively (P < .0001). This validated pediatric DRI, which includes age and residual disease status, can be used to facilitate prognostication and stratification of children with AML and ALL for allogeneic transplantation.
Identifiants
pubmed: 33206937
pii: S0006-4971(21)00320-7
doi: 10.1182/blood.2020009342
pmc: PMC7918183
doi:
Types de publication
Journal Article
Research Support, U.S. Gov't, P.H.S.
Validation Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
983-993Commentaires et corrections
Type : CommentIn
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