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Prepublished online as a Blood First Edition Paper on May 1, 2003; DOI 10.1182/blood-2003-02-0489.
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Blood, 1 September 2003, Vol. 102, No. 5, pp. 1601-1605
CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC
TRIALS
Sirolimus, tacrolimus, and low-dose methotrexate for graft-versus-host disease prophylaxis in mismatched related donor or unrelated donor transplantation
Joseph H. Antin,
Haesook T. Kim,
Corey Cutler,
Vincent T. Ho,
Stephanie J. Lee,
David B. Miklos,
Ephraim P. Hochberg,
Catherine J. Wu,
Edwin P. Alyea, and
Robert J. Soiffer
From the Department of Medical Oncology and Biostatistical Science,
DanaFarber Cancer Institute, Department of Medicine, Brigham & Women's
Hospital, Boston, MA.
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 malignancies 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%), froma5of6 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-I
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.

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