A validated pediatric disease risk index for allogeneic hematopoietic cell transplantation

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 an...

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Veröffentlicht in:Blood 2021-02, Vol.137 (7), p.983-993
Hauptverfasser: Qayed, Muna, Ahn, Kwang Woo, Kitko, Carrie L., Johnson, Mariam H., Shah, Nirali N., Dvorak, Christopher, Mellgren, Karin, Friend, Brian D., Verneris, Michael R., Leung, Wing, Toporski, Jacek, Levine, John, Chewning, Joseph, Wayne, Alan, Kapoor, Urvi, Triplett, Brandon, Schultz, Kirk R., Yanik, Gregory A., Eapen, Mary
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Sprache:eng
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Zusammenfassung: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 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. •The pediatric DRI stratified children with AML and ALL into clinically distinct risk groups based on pretransplantation information.•Risk stratification was based on age at transplant, cytogenetics, and disease status including minimal residual disease at transplant. [Display omitted]
ISSN:0006-4971
1528-0020
DOI:10.1182/blood.2020009342