Volume 120, Issue 2 pp. 304-309

Allogeneic haematopoietic stem cell transplantation for the treatment of adult T-cell leukaemia/lymphoma

Masahiro Kami

Masahiro Kami

Department of Haematology, Toranomon Hospital,

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Tamae Hamaki

Tamae Hamaki

Department of Haematology, Toranomon Hospital,

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Shigesaburo Miyakoshi

Shigesaburo Miyakoshi

Department of Haematology, Toranomon Hospital,

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Naoko Murashige

Naoko Murashige

Stem Cell Transplant Unit, National Cancer Centre Hospital, Tokyo,

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Yoshinobu Kanda

Yoshinobu Kanda

Stem Cell Transplant Unit, National Cancer Centre Hospital, Tokyo,

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Ryuji Tanosaki

Ryuji Tanosaki

Stem Cell Transplant Unit, National Cancer Centre Hospital, Tokyo,

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Yoichi Takaue

Yoichi Takaue

Stem Cell Transplant Unit, National Cancer Centre Hospital, Tokyo,

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Shuichi Taniguchi

Shuichi Taniguchi

Division of Haematology, Hamano-machi Hospital, Fukuoka,

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Hisamaru Hirai

Hisamaru Hirai

Department of Haematology and Oncology, University of Tokyo Hospital, Tokyo,

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Keiya Ozawa

Keiya Ozawa

Division of Cell Transplantation and Transfusion, Jichi Medical School, Tochigi, and

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Masaharu Kasai

Masaharu Kasai

Department of Internal Medicine, Sapporo Hokuyu Hospital, Hokkaido, Japan

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First published: 24 January 2003
Citations: 81
Dr Masahiro Kami, Department of Medical Oncology, Haematopoietic Stem Cell Transplantation Unit, National Cancer Centre Hospital, 5-1-1 Tsjukiji, Chuo-ku, Tokyo 104–0045, Japan. E-mail: [email protected]

Abstract

Summary. The feasibility of allogeneic haematopoietic stem-cell transplantation (allo-HSCT) in 11 patients with adult T-cell leukaemia/lymphoma (ATL) (6 acute, 4 lymphoma, 1 chronic type) was evaluated. The preparative regimens (9 conventional, 2 reduced-intensity) were tolerable. Five patients developed acute graft-versus-host disease (GVHD), and three, extensive chronic GVHD. All 10 patients who survived > 30 d achieved complete remission. Estimated 1-year overall and disease-free survival rates were 53 ± 30% and 45 ± 29% respectively. Four patients remain alive and disease-free at a median follow-up of 25 months. The others died of transplantation-related complications. This pilot study suggests that allo-HSCT in ATL should be evaluated further.

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