Abstract
The outcome of 55 children with severe aplastic anemia (SAA) who received a second hematopoietic stem cell transplantation (HSCT) was retrospectively analyzed using the registration data of the Japanese Society for Hematopoietic Cell Transplantation. The 5-year overall survival (OS) and failure-free survival (FFS) after the second transplantation were 82.9% (95% confidence interval (CI), 69.7–90.8)) and 81.2% (95% CI, 67.8–89.4), respectively. FFS was significantly better when the interval between the first and second transplantation was >60 days (88.9%; 95% CI, 73.0–95.7) than when it was ⩽60 days (61.4%; 95% CI, 33.3–80.5; P=0.026). All 12 patients who were conditioned with regimens containing fludarabine and melphalan were alive with hematopoietic recovery. These findings justify the recommendation of a second HSCT for children with SAA who have experienced graft failure after first HSCT.
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Acknowledgements
We thank all participating doctors and patients who were involved in the Japanese Hematopoietic Cell Transplantation Registry. This work was supported in part by a Research Grant for Allergic Disease and Immunology from the Japanese Ministry of Health, Labor and Welfare.
Author Contributions
KazK and SK designed the research, analyzed the data and wrote the manuscript. HM, NY, RK, HY, KT, KKoh, YT, YC, KeiK, YH, MI, HS, KKawa and KojiK collected and managed the clinical data and discussed the results. RS supervised the data analyses.
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Kudo, K., Muramatsu, H., Yoshida, N. et al. Second allogeneic hematopoietic stem cell transplantation in children with severe aplastic anemia. Bone Marrow Transplant 50, 1312–1315 (2015). https://doi.org/10.1038/bmt.2015.153
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DOI: https://doi.org/10.1038/bmt.2015.153
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