Publication:
Allogeneic Matched Related Donor Bone Marrow Transplantation for Pediatric Patients with Severe Aplastic Anemia Using "low-dose" Cyclophosphamide, ATG Plus Fludarabine

dc.contributor.authorChayamon Takpraditen_US
dc.contributor.authorSusan E. Prockopen_US
dc.contributor.authorNancy A. Kernanen_US
dc.contributor.authorAndromachi Scaradavouen_US
dc.contributor.authorKevin Curranen_US
dc.contributor.authorJulianne Ruggieroen_US
dc.contributor.authorNicole Zakaken_US
dc.contributor.authorRichard J. O'Reillyen_US
dc.contributor.authorFarid Bouladen_US
dc.contributor.otherNew York Presbyterian Hospitalen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.contributor.otherMemorial Sloan-Kettering Cancer Centeren_US
dc.date.accessioned2019-08-28T06:37:23Z
dc.date.available2019-08-28T06:37:23Z
dc.date.issued2018-01-01en_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.citationJournal of Pediatric Hematology/Oncology. Vol.40, No.4 (2018), e220-e224en_US
dc.identifier.doi10.1097/MPH.0000000000001106en_US
dc.identifier.issn15363678en_US
dc.identifier.issn10774114en_US
dc.identifier.other2-s2.0-85046247549en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/47199
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85046247549&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleAllogeneic Matched Related Donor Bone Marrow Transplantation for Pediatric Patients with Severe Aplastic Anemia Using "low-dose" Cyclophosphamide, ATG Plus Fludarabineen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85046247549&origin=inwarden_US

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