Reduced-intensity allogenic transplantation for children and adolescents with Philadelphia chromosome-positive acute lymphoblastic leukemia
- PMID: 38006571
- DOI: 10.1007/s00277-023-05557-z
Reduced-intensity allogenic transplantation for children and adolescents with Philadelphia chromosome-positive acute lymphoblastic leukemia
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.
Keywords: Adolescent; Child; Lymphoid leukemia; Philadelphia chromosome; Stem cell transplantation.
© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
References
-
- Pui C-H, Relling MV, Downing JR (2004) Acute lymphoblastic leukemia. New England J Med 350:1535–1548. https://doi.org/10.1056/NEJMra023001 - DOI
-
- Aricò M, Valsecchi MG, Camitta B et al (2000) Outcome of treatment in children with Philadelphia chromosome–positive acute lymphoblastic leukemia. New England J Med 342:998–1006. https://doi.org/10.1056/NEJM200004063421402 - DOI
-
- Aricò M, Schrappe M, Hunger SP et al (2010) Clinical outcome of children with newly diagnosed Philadelphia chromosome–positive acute lymphoblastic leukemia treated between 1995 and 2005. J Clin Oncol 28:4755–4761. https://doi.org/10.1200/JCO.2010.30.1325 - DOI - PubMed - PMC
-
- Schultz KR, Bowman WP, Aledo A et al (2009) Improved early event-free survival with imatinib in Philadelphia chromosome–positive acute lymphoblastic leukemia: a children’s oncology group study. J Clin Oncol 27:5175–5181. https://doi.org/10.1200/JCO.2008.21.2514 - DOI - PubMed - PMC
-
- Biondi A, Schrappe M, de Lorenzo P et al (2012) Imatinib after induction for treatment of children and adolescents with Philadelphia-chromosome-positive acute lymphoblastic leukaemia (EsPhALL): a randomised, open-label, intergroup study. Lancet Oncol 13:936–945. https://doi.org/10.1016/S1470-2045(12)70377-7 - DOI - PubMed - PMC
MeSH terms
LinkOut - more resources
Full Text Sources