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      Thymoglobulin prevents chronic graft-versus-host disease, chronic lung dysfunction, and late transplant-related mortality: long-term follow-up of a randomized trial in patients undergoing unrelated donor transplantation.

      Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
      Adolescent, Adult, Antilymphocyte Serum, therapeutic use, Bone Marrow Transplantation, adverse effects, mortality, Cause of Death, Chronic Disease, Cyclosporine, administration & dosage, Drug Therapy, Combination, Female, Follow-Up Studies, Forced Expiratory Volume, Graft vs Host Disease, prevention & control, Humans, Immunosuppressive Agents, Incidence, Karnofsky Performance Status, Leukemia, surgery, Life Tables, Lung Diseases, etiology, physiopathology, Male, Methotrexate, Middle Aged, Neural Tube Defects, Premedication, Prospective Studies, Recurrence, Survival Analysis, T-Lymphocytes, immunology, Transplantation, Homologous, Treatment Outcome, Vital Capacity

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          Abstract

          This is an update of a randomized study on antithymocyte globulin (ATG; Thymoglobulin) before transplantation in patients undergoing unmanipulated marrow transplantation from unrelated donors. The median follow-up for surviving patients is 5.7 years. At last follow-up, chronic graft-versus-host disease (GVHD) was scored in 60% of non-ATG and in 37% of ATG patients (P=.05), and extensive chronic GVHD was present in 41% and 15%, respectively (P=.01). Chronic lung dysfunction was diagnosed in 51% versus 19% of patients (P=.005). Forced vital capacity decreased significantly with time in non-ATG patients (P=.005), but not in patients who received ATG (P=.30). The proportion of patients with Karnofsky scores of >or=90% at 4 years was 57% versus 89% in non-ATG versus ATG patients (P=.03). The actuarial 6-year survival for all patients randomized was 31% versus 44% (non-ATG versus ATG; P=.80). The cumulative incidence of transplant-related mortality was 51% versus 41% (P=.70) and of relapse was 32% versus 40% (P=.90). For patients who survived 1 year, transplant-related mortality was 25% versus 3% (P=.03), and actuarial survival was 58% versus 85% (P=.09). In conclusion, the addition of ATG to cyclosporine/methotrexate provides significant protection against extensive chronic GVHD and chronic lung dysfunction, reduces late transplant mortality, and improves quality of life in patients undergoing unrelated donor transplantation.

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