Reduced-intensity allogenic transplantation for children and adolescents with Philadelphia chromosome-positive acute lymphoblastic leukemia
Hisashi Ishida1, Yuki Arakawa2, Daiichiro Hasegawa3
1Department of Pediatrics, Okayama University Hospital, Okayama, Japan.
Insights
Reduced-intensity conditioning (RIC) for hematopoietic stem cell transplantation (HSCT) in pediatric Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL) showed comparable leukemia-free survival to myeloablative conditioning (MAC). RIC emerged as a favorable prognostic factor, suggesting its potential use in this patient group.
Area of Science:
- Hematology
- Oncology
- Transplantation Medicine
Background:
- Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL) survival has improved with tyrosine kinase inhibitors (TKI).
- Hematopoietic stem cell transplantation (HSCT) remains crucial for Ph+ALL management.
- Reduced-intensity conditioning (RIC) is common for older HSCT patients, but its use in pediatric Ph+ALL is understudied.
Purpose of the Study:
- To evaluate the efficacy of RIC versus myeloablative conditioning (MAC) in young patients with Ph+ALL undergoing HSCT.
- To identify prognostic factors for leukemia-free survival (LFS) in this population.
Main Methods:
- Retrospective analysis of nationwide Japanese registry data.
- Inclusion of patients (<25 years) with de novo Ph+ALL in first or second remission, receiving HSCT with pre-HSCT TKI therapy.
- Comparison of outcomes between MAC (n=265) and RIC (n=33) regimens.
Main Results:
- Five-year LFS rates were 67.3% for MAC and 79.8% for RIC (p=0.142).
- Multivariate analysis identified RIC as a significant favorable prognostic factor for LFS (HR 0.32, p=0.032) in patients with good performance status.
- Similar favorable trends for RIC were observed with prophylactic post-HSCT TKI maintenance.
Conclusions:
- HSCT with RIC demonstrates comparable LFS to MAC in young Ph+ALL patients.
- RIC is an independent favorable prognostic factor for LFS in this cohort.
- RIC, especially with post-HSCT TKI maintenance, may be a safe and effective option for pediatric and adolescent Ph+ALL patients.
Abstract:
Survival rates of patients with Philadelphia chromosome-positive ALL (Ph+ALL) have improved considerably with the introduction of tyrosine kinase inhibitors (TKI); however, hematopoietic stem cell transplantation (HSCT) continues to play an important role. Reduced-intensity conditioning (RIC) regimens have been widely applied particularly for older patients, but their validity for children and adolescents with Ph+ALL has not been investigated. In this study, data from patients receiving HSCT for de novo Ph+ALL in first or second remission at ages younger than 25 years and with a history of pre-HSCT TKI therapy were retrospectively collected through the nationwide registry in Japan. In 265 patients who received myeloablative conditioning (MAC) and 33 patients receiving RIC, 5-year leukemia-free survival (LFS) rates were 67.3% and 79.8%, respectively (p = 0.142). Multivariate analysis of LFS, focusing on patients with good performance status, identified RIC as a significant prognostic factor for LFS (hazard ratio 0.32, p = 0.032), as well as older age, higher leukocyte count at diagnosis, and disease with additional chromosomal abnormalities. These trends were similar when we focused on patients who received prophylactic post-HSCT TKI treatment, as 5-year LFS was 81.0% for MAC and 84.4% for RIC (p = 0.748). In summary, HSCT with RIC regimen showed at least comparable LFS to HSCT with MAC regimen, and RIC was an independent favorable prognostic factor on multivariate analysis adjusting potential prognostic factors. While patient numbers were limited, our data suggest that RIC may be safely applied in this group, particularly combined with prophylactic post-HSCT TKI maintenance therapy.
More Related Videos
07:39Intracellular Phosphoflow Cytometry of Acute Myeloid Leukemia Patient-Derived Xenotransplants
Published on: June 6, 2025
06:08Assessment of Chimeric Antigen Receptor T Cell-Associated Toxicities Using an Acute Lymphoblastic Leukemia Patient-Derived Xenograft Mouse Model
Published on: February 10, 2023
