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Haematologica, Vol 91, Issue 5, 667-670
Copyright © 2006 by Ferrata Storti Foundation


Clinical Trial, Phase II

Antithymocyte globulin and cyclosporine A as combination therapy for low-risk non-sideroblastic myelodysplastic syndromes

PA Broliden, IM Dahl, R Hast, B Johansson, E Juvonen, L Kjeldsen, A Porwit-MacDonald, M Sjoo, JM Tangen, B Uggla, G Oberg, and E Hellstrom-Lindberg

Karolinska Institutet, Department of Medicine, Karolinska University, Hospital Huddinge, Stockholm, Sweden.

The present study evaluated the combination of antithymocyte globulin (ATG) and cyclosporine A (CsA) in patients with low-risk myelodysplastic syndromes. Twenty patients (17 with refractory anemia and 3 with refractory anemia with excess blasts) received treatment with rabbit-ATG plus CsA. The overall response rate was 30% (6/20); three of the six responders had a complete response. The responses lasted 2-58 months, with two patients still being in complete remission at 42 and 58 months. Short-lasting cytogenetic remissions were achieved in two patients. ATG was poorly tolerated in patients over 70 years of age. Four out of 20 patients progressed to acute myeloid leukemia within a year. We conclude that immunosuppressive treatment may be a therapeutic option for selected patients with myelodysplastic syndrome.


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