We studied the feasibility and activity of adding sirolimus to tacrolimus and low-dose methotrexate as graft-versus-host disease (GVHD) prophylaxis in recipients of alternative donor transplants. Forty-one patients with hematologic malignaincies were conditioned with cyclophosphamide and total body irradiation. Marrow stem cells were from an HLA-A, -B, and -DR compatible, unrelated donor (n = 26, 68%), from a 5 of 6 antigen-matched unrelated donor (n = 8, 20%), or from a 5 of 6 antigen-matched family member (n = 5, 12%). Therapeutic serum levels of sirolimus were attained in most patients. All evaluable patients engrafted. An absolute neutrophil count of 500/μL was achieved on day +18 (range, 11-32 days). Sustained platelet counts of more than 20 000/μL were attained on day +29 (range, 14-98 days). Grades 0-1 acute GVHD occurred in 75% of patients. Grades II, III, and IV acute GVHD occurred in 13%, 8%, and 5%, respectively (total grades II-IV GVHD, 26%), Median survival is 366 days (95% CI 185, not estimable) and actuarial survival at 1 year is 52%. Oral sirolimus is tolerable, adequate blood levels are achievable, and there is a low rate of acute GVHD compared with historical data in this high-risk population. This novel agent is worthy of further study in allogeneic transplantation. © 2003 by The American Society of Hematology.
CITATION STYLE
Antin, J. H., Kim, H. T., Cutler, C., Ho, V. T., Lee, S. J., Miklos, D. B., … Soiffer, R. J. (2003). Sirolimus, tacrolimus, and low-dose methotrexate for gaft-versus-host disease prophylaxis in mismatched related donor or unrelated donor transplantation. Blood, 102(5), 1601–1605. https://doi.org/10.1182/blood-2003-02-0489
Mendeley helps you to discover research relevant for your work.