| Literature DB >> 24304374 |
Biju George1, Vikram Mathews, Kavitha M Lakshmi, Sameer Melinkeri, Ajay Sharma, Auro Viswabandya, Sanjeevan Sharma, Satyaranjan Das, Rayaz Ahmed, Aby Abraham, Velu Nair, Shashikant Apte, Mammen Chandy, Alok Srivastava.
Abstract
Between 2001 and 2009, 121 patients with severe aplastic anemia (SAA) underwent hematopoietic stem cell transplantation (HSCT) using a conditioning protocol of fludarabine and cyclophosphamide at three Indian hospitals. Donors were HLA-identical sibling or family donors. Seventy-six patients were considered "high risk" as per criteria. The graft source included peripheral blood stem cells in 109 and G-CSF-stimulated bone marrow in 12. GVHD prophylaxis consisted of cyclosporine and mini-methotrexate. Engraftment occurred in 117 (96.6%) while two had graft failure and two expired in the first two wk. Neutrophil engraftment was seen at 12.3 d (range: 9-19) while platelet engraftment occurred at 12.4 d (range: 8-32). Grade II-IV acute GVHD was seen in 26.7% and grade IV GVHD in 8.6%. Chronic GVHD occurred in 44% and was extensive in 10%. The five-yr overall survival for the entire cohort is 75.8 ± 3.9% with a survival of 95.6 ± 3.1% in the low-risk group (n = 45) and 64.0 ± 5.6% in the high-risk group (n = 76). Conditioning with fludarabine and cyclophosphamide is associated with very good long-term survival in patients undergoing HSCT for SAA.Entities:
Keywords: aplastic anemia; fludarabine; survival; transplant
Mesh:
Substances:
Year: 2013 PMID: 24304374 DOI: 10.1111/ctr.12263
Source DB: PubMed Journal: Clin Transplant ISSN: 0902-0063 Impact factor: 2.863