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Allogeneic stem cell transplantation for patients with aggressive NK-cell leukemia.
Fujimoto, Ayumi; Ishida, Fumihiro; Izutsu, Koji; Yamasaki, Satoshi; Chihara, Dai; Suzumiya, Junji; Mitsui, Tetsuo; Doki, Noriko; Sakai, Hitoshi; Kobayashi, Hikaru; Kanda, Junya; Fukuda, Takahiro; Atsuta, Yoshiko; Suzuki, Ritsuro.
Afiliação
  • Fujimoto A; Department of Oncology and Hematology, Shimane University Hospital, Izumo, Japan.
  • Ishida F; Department of Biomedical Laboratory Sciences, Shinshu University School of Medicine, Matsumoto, Japan.
  • Izutsu K; Division of Hematology, Department of Internal Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
  • Yamasaki S; Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.
  • Chihara D; Department of Hematology and Clinical Research Institute, National Hospital Organization Kyushu Medical Center, Fukuoka, Japan.
  • Suzumiya J; Medical Oncology Service, National Institute of Health, Bethesda, MD, USA.
  • Mitsui T; Department of Oncology and Hematology, Shimane University Hospital, Izumo, Japan.
  • Doki N; Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan.
  • Sakai H; Hematology Division, Tokyo Metropolitan Cancer and Infectious Disease Center, Komagome Hospital, Tokyo, Japan.
  • Kobayashi H; Division of Hematology, Department of Internal Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
  • Kanda J; Department of Hematology, Nagano Red Cross Hospital, Nagano, Japan.
  • Fukuda T; Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Atsuta Y; Department of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
  • Suzuki R; Japanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan.
Bone Marrow Transplant ; 56(2): 347-356, 2021 02.
Article em En | MEDLINE | ID: mdl-32778688
Aggressive NK-cell leukemia (ANKL) has a fulminant clinical course with a poor prognosis. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is currently the only curative treatment. Using the Japanese transplant registry data, the outcomes of 59 ANKL patients who underwent first allo-HSCT were analyzed. Twenty-nine patients received stem cells from cord blood (CB), 18 from peripheral blood, and 12 from bone marrow. At the time of transplant 21 patients had complete response (CR), and 7 partial response (PR), but 31 without response. The 1-year and 5-year overall survival (OS) were 33.9% and 27.3%, respectively. The 1-year cumulative incidences of relapse or progression was 55.5%, and that of non-relapse mortality was 12.1%. The OS was significantly better for patients with CR or PR at the time of allo-HSCT (P = 0.046), which was equivalent to that for patients who experienced primary induction failure at the time of allo-HSCT but achieved CR afterwards (40.6% versus 32.0% at 5 years; P = 0.95). Patients receiving CB had a significantly better OS than those receiving stem cells from others (37.3% versus 16.2% at 5 years; P = 0.04). Patients achieving event-free survival at 12 months after allo-HSCT had good outcomes with 5-year OS of 85.2%.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Prolinfocítica de Células T / Transplante de Células-Tronco Hematopoéticas / Leucemia Linfocítica Granular Grande Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Prolinfocítica de Células T / Transplante de Células-Tronco Hematopoéticas / Leucemia Linfocítica Granular Grande Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article