Your browser doesn't support javascript.
loading
A US Multicenter Collaborative Study on Outcomes of Hematopoietic Cell Transplantation in Hepatosplenic T-Cell Lymphoma.
Moustafa, Muhamad Alhaj; Ramdial, Jeremy L; Tsalatsanis, Athanasios; Khimani, Farhad; Dholaria, Bhagirathbhai; Bojanini, Leyla; Brooks, Taylor Rey; Zain, Jasmine; Bennani, N Nora; Braunstein, Zachary; Brammer, Jonathan E; Beitinjaneh, Amer; Jagadeesh, Deepa; Weng, Wen Kai; Kumar, Ambuj; Kharfan-Dabaja, Mohamed A; Ahmed, Sairah; Murthy, Hemant S.
Afiliación
  • Moustafa MA; Division of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, Florida.
  • Ramdial JL; Department of Lymphoma/Myeloma and Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Tsalatsanis A; Department of Internal Medicine, Research Methodology and Biostatistics Core, Office of Research, University of South Florida Morsani College of Medicine, Tampa, Florida.
  • Khimani F; Blood and Marrow Transplantation and Cellular Immunotherapy, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Dholaria B; Medicine, Division of Hematology/Oncology, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Bojanini L; Stanford University School of Medicine, Palo Alto, California.
  • Brooks TR; Hematology and Medical Oncology, Cleveland Clinic, Cleveland, Ohio.
  • Zain J; Hematology/Hematopoietic Cell Transplant, City of Hope National Medical Center, Duarte, California.
  • Bennani NN; Hematology, Mayo Clinic, Rochester, Minnesota.
  • Braunstein Z; Department of Internal Medicine, Ohio State University Wexner Medical Columbus, Columbus, Ohio.
  • Brammer JE; Division of Hematology, Department of Internal Medicine, James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
  • Beitinjaneh A; Division of Transplantation and Cellular Therapy, University of Miami, Miami, Florida.
  • Jagadeesh D; Hematology and Medical Oncology, Cleveland Clinic, Cleveland, Ohio.
  • Weng WK; Division of BMT and Cellular Therapy, Stanford University School of Medicine, Stanford, California.
  • Kumar A; Department of Internal Medicine, Research Methodology and Biostatistics Core, Office of Research, University of South Florida Morsani College of Medicine, Tampa, Florida.
  • Kharfan-Dabaja MA; Division of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, Florida.
  • Ahmed S; Department of Lymphoma/Myeloma and Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Murthy HS; Division of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, Florida. Electronic address: Murthy.hemant@mayo.edu.
Transplant Cell Ther ; 30(5): 516.e1-516.e10, 2024 May.
Article en En | MEDLINE | ID: mdl-38431075
ABSTRACT
Hepatosplenic T-cell lymphoma (HSTCL) is a rare and aggressive type of peripheral T-cell lymphoma with median overall survival (OS) of approximately 1 year. Data on the effectiveness of hematopoietic cell transplantation (HCT) is limited, as is the choice between autologous HCT (auto-HCT) and allogeneic HCT (allo-HCT) in the treatment of this disease. To evaluate the outcome of patients with HSTCL who underwent either auto-HCT or allo-HCT, we performed a multi-institutional retrospective cohort study to assess outcomes of HCT in HSTCL patients. Fifty-three patients with HSTCL were included in the study. Thirty-six patients received an allo-HCT and 17 received an auto-HCT. Thirty-five (66%) were males. Median age at diagnosis was 38 (range 2 to 64) years. Median follow-up for survivors was 75 months (range 8 to 204). The median number of prior lines of therapy was 1 (range 1 to 4). Median OS and progression-free survival (PFS) for the entire cohort were 78.5 months (95% CI 25 to 79) and 54 months (95% CI 18 to 75), respectively. There were no significant differences in OS (HR 0.63, 95% CI 0.28 to 1.45, P = .245) or PFS (HR 0.7, 95% CI 0.32 to 1.57, P = .365) between the allo-HCT and auto-HCT groups, respectively. In the allo-HCT group, the 3-year cumulative incidence of relapse was 35% (95% CI 21 to 57), while 3-year cumulative incidence of NRM was 16% (95% CI 7 to 35). In the auto-HCT group, the 3-year cumulative incidence of relapse and NRM were 43% (95% CI 23 to 78) and 14% (95% CI 4 to 52), respectively. Both Auto-HCT and Allo-HCT are effective consolidative strategies in patients with HSTCL, and patients should be promptly referred for HCT evaluation.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Transplant Cell Ther Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Transplant Cell Ther Año: 2024 Tipo del documento: Article
...