Personalized Prognostic Risk Score for Long-Term Survival for Children with Acute Leukemia after Allogeneic
Menachem Bitan1, Kwang Woo Ahn2, Heather R Millard3
1Department of Pediatric Hematology/Oncology, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.
We developed risk scores to predict survival in children with acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) post-transplant. These scores identify high-risk patients for targeted interventions to improve long-term outcomes.
Area of Science:
- Pediatric Hematology Oncology
- Stem Cell Transplantation
- Leukemia Research
Background:
- Hematopoietic stem cell transplantation (HSCT) is a critical curative option for pediatric leukemia.
- Long-term survival and risk stratification are essential for optimizing post-transplant care in children with acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL).
Purpose of the Study:
- To identify prognostic factors influencing leukemia-free survival (LFS) and overall survival (OS) in pediatric AML and ALL patients post-HSCT.
- To develop and validate risk scores for predicting long-term survival after related or unrelated donor transplantation.
Main Methods:
- Retrospective analysis of 790 AML and 1096 ALL patients transplanted between 2000-2010, surviving at least 1 year in remission.
- Evaluation of patient, disease, transplantation characteristics, and graft-versus-host disease (GVHD) to determine adverse prognostic factors.
- Development of risk scores for AML and ALL based on identified prognostic factors.
Main Results:
- For AML, risk score components include age, disease status, cytogenetic risk, and chronic GVHD. For ALL, risk score components include age and chronic GVHD.
- 10-year OS probabilities for AML: 94% (good risk), 87% (intermediate risk), 68% (poor risk).
- 10-year OS probabilities for ALL: 89% (good risk), 80% (poor risk).
Conclusions:
- Established risk scores effectively stratify long-term survival probabilities for pediatric AML and ALL patients post-HSCT.
- Early identification of high-risk children can guide interventions to mitigate late mortality.
- Prognostic factors beyond 4 years for AML and 3 years for ALL were not significant.
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