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Allogeneic stem cell transplantation for severe acquired aplastic anaemia using a fludarabine‐based preparative regimen
Author(s) -
Resnick Igor B.,
Aker Memet,
Shapira Michael Y.,
Tsirigotis Panagiotis D.,
Bitan Menachem,
AbdulHai Ali,
Samuel Simcha,
Ackerstein Aliza,
Gesundheit Benjamin,
Zilberman Irina,
Miron Svetlana,
Yoffe Luba,
Lvovich Alex,
Slavin Shimon,
Or Reuven
Publication year - 2006
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.2006.06084.x
Subject(s) - medicine , fludarabine , cumulative incidence , regimen , mucositis , cyclophosphamide , transplantation , surgery , hematopoietic stem cell transplantation , incidence (geometry) , aplastic anemia , gastroenterology , graft versus host disease , busulfan , total body irradiation , toxicity , chemotherapy , bone marrow , physics , optics
Summary We reviewed our experience in the treatment of 13 patients with severe acquired aplastic anaemia, using a newly developed non‐myeloablative regimen consisting of fludarabine (total dose 180 mg/m 2 ), cyclophosphamide (total dose 120 mg/kg), and antithymocyte globulin (total dose 40 mg/kg). All except one patient received multiple transfusions and had failed prior immunosuppressive treatment. Twelve out of 13 patients achieved sustained engraftment. One patient was not evaluable for engraftment because of early death on day +10. None of the patients developed graft failure. Mucositis of mild‐to‐moderate severity was the only observed regimen‐related toxicity. The cumulative incidence of acute graft‐ versus ‐host disease (GvHD) grade II–IV and III–IV was 8·3% and 0%, respectively. With a median follow‐up period of 45 months, the 5‐year overall survival probability was 84%. Eight out of 11 surviving patients have been followed for more than 1 year and only one developed limited chronic GvHD. All patients enjoy a normal life style, with a Karnofsky score of 100%, and all except three, followed for 3, 5 and 6 months respectively, are free of any immunosuppressive medication. The results of this study look promising, while prospective clinical trials may be required to confirm the benefits of this regimen as an alternative to existing protocols.