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Allogeneic stem-cell transplantation in patients with cutaneous lymphoma: updated results from a single institution.
Hosing, C; Bassett, R; Dabaja, B; Talpur, R; Alousi, A; Ciurea, S; Popat, U; Qazilbash, M; Shpall, E J; Oki, Y; Nieto, Y; Pinnix, C; Fanale, M; Maadani, F; Donato, M; Champlin, R; Duvic, M.
Afiliación
  • Hosing C; Department of Stem Cell Transplantation and Cellular Therapy cmhosing@mdanderson.org.
  • Bassett R; Department of Biostatistics.
  • Dabaja B; Department of Radiation Oncology.
  • Talpur R; Department of Dermatology.
  • Alousi A; Department of Stem Cell Transplantation and Cellular Therapy.
  • Ciurea S; Department of Stem Cell Transplantation and Cellular Therapy.
  • Popat U; Department of Stem Cell Transplantation and Cellular Therapy.
  • Qazilbash M; Department of Stem Cell Transplantation and Cellular Therapy.
  • Shpall EJ; Department of Stem Cell Transplantation and Cellular Therapy.
  • Oki Y; Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.
  • Nieto Y; Department of Stem Cell Transplantation and Cellular Therapy.
  • Pinnix C; Department of Radiation Oncology.
  • Fanale M; Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.
  • Maadani F; Department of Stem Cell Transplantation and Cellular Therapy.
  • Donato M; Department of Blood and Marrow Transplantation, John Theurer Cancer Center, Hackensack, USA.
  • Champlin R; Department of Stem Cell Transplantation and Cellular Therapy.
  • Duvic M; Department of Dermatology.
Ann Oncol ; 26(12): 2490-5, 2015 Dec.
Article en En | MEDLINE | ID: mdl-26416896
ABSTRACT

BACKGROUND:

Cutaneous T-cell lymphomas (CTCLs) and its common variants mycosis fungoides (MF) and leukemic Sézary syndrome (SS) are rare extranodal non-Hodgkin's lymphomas. Patients who present with advanced disease and large-cell transformation (LCT) are incurable with standard treatments. In this article, we report the largest single-center experience with allogeneic stem-cell transplantation (SCT) for advanced CTCL. PATIENTS AND

METHODS:

This is a prospective case series of 47 CTCL patients who underwent allogeneic SCT after failure of standard therapy between July 2001 and September 2013. The Kaplan-Meier method was used to estimate overall survival (OS) and progression-free survival (PFS) curves. The method of Fine and Gray was used to fit regression models to the same covariates for these cumulative incidence data.

RESULTS:

The Kaplan-Meier estimates of OS and PFS at 4 years were 51% and 26%, respectively. There was no statistical difference in the OS in patients who had MF alone, SS, MF with LCT, or SS with LCT. PFS at 4 years was superior in patients who had SS versus those who did not (52.4% versus 9.9%; P = 0.02). The cumulative incidences of grade 2-4 acute graft-versus-host disease (GVHD) and chronic GVHD were 40% and 28%, respectively. The cumulative nonrelapse mortality rate was 16.7% at 2 years.

CONCLUSION:

Allogeneic SCT may result in long-term remissions in a subset of patients with advanced CTCL. Although post-SCT relapse rates are high, many patients respond to immunomodulation and achieve durable remissions. CLINICALTRIALSGOV NCT00506129.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Linfoma Cutáneo de Células T / Trasplante de Células Madre Hematopoyéticas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Linfoma Cutáneo de Células T / Trasplante de Células Madre Hematopoyéticas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2015 Tipo del documento: Article