Publication: Allogeneic Matched Related Donor Bone Marrow Transplantation for Pediatric Patients with Severe Aplastic Anemia Using "low-dose" Cyclophosphamide, ATG Plus Fludarabine
dc.contributor.author | Chayamon Takpradit | en_US |
dc.contributor.author | Susan E. Prockop | en_US |
dc.contributor.author | Nancy A. Kernan | en_US |
dc.contributor.author | Andromachi Scaradavou | en_US |
dc.contributor.author | Kevin Curran | en_US |
dc.contributor.author | Julianne Ruggiero | en_US |
dc.contributor.author | Nicole Zakak | en_US |
dc.contributor.author | Richard J. O'Reilly | en_US |
dc.contributor.author | Farid Boulad | en_US |
dc.contributor.other | New York Presbyterian Hospital | en_US |
dc.contributor.other | Faculty of Medicine, Siriraj Hospital, Mahidol University | en_US |
dc.contributor.other | Memorial Sloan-Kettering Cancer Center | en_US |
dc.date.accessioned | 2019-08-28T06:37:23Z | |
dc.date.available | 2019-08-28T06:37:23Z | |
dc.date.issued | 2018-01-01 | en_US |
dc.description.abstract | © 2018 Wolters Kluwer Health, Inc. All rights reserved. Background: The combination of cyclophosphamide (CY) and antithymocyte globulin (ATG) has been used as a standard conditioning regimen for matched related donor transplantation in patients with severe aplastic anemia. Procedure: To decrease the regimen-related toxicity while maintaining appropriate engraftment and survival rates, fludarabine (FLU) was added to the regimen. Four pediatric patients received matched related donor bone marrow transplantation with CY (50 mg/kg×2) (instead of the 50 mg/kg×4 standard dosing), equine ATG (30 mg/kg×3), with the addition of FLU (30 mg/m 2 ×4). Graft versus host disease (GvHD) prophylaxis included a calcineurin inhibitor and methotrexate. Results: No grade 4 acute toxicities occurred during the first 30 days after transplant. All patients engrafted with normalization of peripheral blood counts and transfusion independence. One patient developed grade 1 to 2 acute GvHD, followed by chronic GvHD that resolved. With a median follow-up of 41.7 months, all 4 patients are alive and transfusion free, with complete donor chimerism. This combination of a low-dose CY/ATG+FLU regimen was overall very well tolerated and contributed toward a successful outcome including engraftment, chimerism, and survival. Conclusion: This small pilot study shows that this cytoreductive regimen could be considered as the standard of care for transplantation of pediatric patients with aplastic anemia from HLA-matched siblings. | en_US |
dc.identifier.citation | Journal of Pediatric Hematology/Oncology. Vol.40, No.4 (2018), e220-e224 | en_US |
dc.identifier.doi | 10.1097/MPH.0000000000001106 | en_US |
dc.identifier.issn | 15363678 | en_US |
dc.identifier.issn | 10774114 | en_US |
dc.identifier.other | 2-s2.0-85046247549 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/47199 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85046247549&origin=inward | en_US |
dc.subject | Medicine | en_US |
dc.title | Allogeneic Matched Related Donor Bone Marrow Transplantation for Pediatric Patients with Severe Aplastic Anemia Using "low-dose" Cyclophosphamide, ATG Plus Fludarabine | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85046247549&origin=inward | en_US |