Allogeneic hematopoietic stem cell transplantation for ATL with central nervous system involvement: The Nagasaki Transplant Group experience

被引:0
作者
Takuya Fukushima
Jun Taguchi
Yukiyoshi Moriuchi
Shinichiro Yoshida
Hidehiro Itonaga
Koji Ando
Yasushi Sawayama
Yoshitaka Imaizumi
Daisuke Imanishi
Tomoko Hata
Yasushi Miyazaki
机构
[1] Nagasaki University Graduate School of Biomedical Sciences,Department of Hematology, Atomic Bomb Disease and Hibakusya Medicine Unit, Atomic Bomb Disease Institute
[2] Sasebo City General Hospital,undefined
[3] National Hospital Organization Nagasaki Medical Center,undefined
来源
International Journal of Hematology | 2011年 / 94卷
关键词
ATL; CNS involvement; Allo-HSCT;
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学科分类号
摘要
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is regarded as a curative option for aggressive adult T cell leukemia-lymphoma (ATL). However, the efficacy and safety of allo-HSCT for ATL with central nervous system (CNS) involvement, which is highly resistant to chemotherapy, remain controversial. We analyzed 10 ATL patients with CNS involvement who received allo-HSCT at three institutions in Nagasaki prefecture between 2000 and 2007. The 3-year overall survival rate was 40%, and the median observation time of the four surviving patients was 1532 days (range 945–2212 days). Two of four surviving patients received highly intensive local treatment for the CNS; one with 26 intrathecal injections of antineoplastic agents, and the other with whole cerebrospinal irradiation before transplantation. However, the other two patients received conventional or reduced-intensity conditioning with standard intrathecal chemotherapy. Three of the four surviving patients experienced chronic GVHD, and two of three patients with grade 3 or 4 acute GVHD were free from CNS relapse. From these data, it seems that both intensive local treatment for CNS disease and systemic GVHD contributed to the long-term control of CNS involvement. Although our data suggest that allo-HSCT is a therapeutic option for ATL with CNS disease, high transplant-related mortality (six cases) indicates the need for further studies to develop more effective procedures for CNS disease, and to reduce transplant-related morbidity.
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页码:390 / 394
页数:4
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  • [1] Uchiyama T(1977)Adult T-cell leukemia: clinical and hematologic features of 16 cases Blood 50 481-492
  • [2] Yodoi J(1980)Detection and isolation of type C retrovirus particles from fresh and cultured lymphocytes of a patients with cutaneous T-cell lymphoma Proc Natl Acad Sci USA 77 7415-7419
  • [3] Sagawa K(1981)Adult T-cell leukemia: antigen in an ATL cell line and detection of antibodies to the antigen in human sera Proc Natl Acad Sci USA 78 6476-6480
  • [4] Poiesz BJ(1984)Monoclonal integration of human T-cell leukemia provirus in all primary tumors of adult T-cell leukemia suggests causative role of human T-cell leukemia virus in the disease Proc Natl Acad Sci USA 81 2534-2537
  • [5] Ruscetti FW(1988)Major prognostic factors of adult patients with advanced T-cell lymphoma/leukemia J Clin Oncol 6 1088-1097
  • [6] Gazdar AF(1991)Diagnostic criteria and classification of clinical subtypes of adult T-cell leukaemia-lymphoma: a report from the Lymphoma Study Group (1984–87) Br J Haematol 79 428-437
  • [7] Bunn PA(1998)Management of adult T-cell leukaemia/lymphoma Br J Haematol 100 453-458
  • [8] Minna JD(1991)Major prognostic factors of patients with adult T-cell leukemia-lymphoma: a cooperative study-Lymphoma Study Group (1984–87) Leuk Res 15 81-90
  • [9] Gallo RC(1988)Chemotherapy results and prognostic factors of patients with advanced non-Hodgkin’s lymphoma treated with VEPA or VEPA-M J Clin Oncol 6 128-141
  • [10] Hinuma Y(1994)Japan Clinical Oncology Group phase II trial of second-generation “LSG4protocol” in aggressive T- and B-lymphoma: a new predictive model for T- and B-lymphoma Proc Am Soc Clin Oncol 13 378-5464