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Blood, 15 May 2005, Vol. 105, No. 10, pp. 4143-4145. Prepublished online as a Blood First Edition Paper on January 21, 2005; DOI 10.1182/blood-2004-11-4193.
TRANSPLANTATION Allogeneic stem-cell transplantation with reduced conditioning intensity as a novel immunotherapy and antiviral therapy for adult T-cell leukemia/lymphomaFrom the Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka, Japan; Department of Hematology, Imamura Bun-in Hospital, Kagoshima, Japan; Stem Cell Transplantation Unit, National Cancer Center Hospital, Tokyo, Japan; Department of Hematology, National Kyushu Cancer Center, Fukuoka, Japan; Department of Virology, Faculty of Medicine, Kagoshima University, Kagoshima, Japan; Department of Immunotherapeutics, Tokyo Medical and Dental University, Medical Research Division, Tokyo, Japan; Department of Hematology, Molecular Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University School of Medicine, Nagasaki, Japan; Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan; First Department of Internal Medicine, Fukuoka University, Fukuoka, Japan; Second Department of Internal Medicine, University of the Ryukyus, Okinawa, Japan; Institute for Clinical Research, Kumamoto National Hospital, Kumamoto, Japan; Blood Transfusion Service, Oita University, Faculty of Medicine, Oita, Japan; Department of Hematology, Oita Prefectural Hospital, Oita, Japan.
Sixteen patients with adult T-cell leukemia/lymphoma (ATL) who were all over 50 years of age underwent allogeneic stem cell transplantation with reduced-conditioning intensity (RIST) from HLA-matched sibling donors after a conditioning regimen consisting of fludarabine (180 mg/m2), busulfan (8 mg/kg), and rabbit antithymocyte globulin (5 mg/kg). The observed regimen-related toxicities and nonhematologic toxicities were all found to be acceptable. Disease relapse was the main cause of treatment failure. Three patients who had a relapse subsequently responded to a rapid discontinuation of the immunosuppressive agent and thereafter achieved another remission. After RIST, the human T-cell leukemia virus type 1 (HTLV-1) proviral load became undetectable in 8 patients. RIST is thus considered to be a feasible treatment for ATL. Our data also suggest the presence of a possible graft-versus-ATL effect; an anti-HTLV-1 activity was also found to be associated with this procedure.
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