| Literature DB >> 20018919 |
Robert A Brodsky1, Allen R Chen, Donna Dorr, Ephraim J Fuchs, Carol Ann Huff, Leo Luznik, B Douglas Smith, William H Matsui, Steven N Goodman, Richard F Ambinder, Richard J Jones.
Abstract
Severe aplastic anemia (SAA) is a life-threatening bone marrow failure disorder that can be treated with bone marrow transplantation, immunosuppressive therapy, and high-dose cyclophosphamide. Here, we report long-term follow-up on 67 SAA patients (44 treatment-naive and 23 refractory) treated with high-dose cyclophosphamide. At 10 years, the overall actuarial survival was 88%, the response rate was 71% with the majority being complete, and the actuarial event-free survival was 58% in 44 treatment-naive SAA patients. Patients with refractory SAA fared less well after high-dose cyclophosphamide therapy; at 10 years, overall actuarial survival, response, and actuarial event-free survival rates were 62%, 48%, and 27%, respectively. High-dose cyclophosphamide is highly effective therapy for severe aplastic anemia. Large randomized controlled trials will be necessary to establish how results of high-dose cyclophosphamide compare with either bone marrow transplantation or standard immunosuppressive regimens, such as antithymocyte globulin and cyclosporine.Entities:
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Year: 2009 PMID: 20018919 PMCID: PMC2844020 DOI: 10.1182/blood-2009-06-225375
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113