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Allogeneic hematopoietic stem cell transplantation in patients with advanced indolent lymphoproliferative disorders

BACKGROUND: The role of allogeneic hematopoietic stem cell transplantation for advanced indolent lymphoproliferative disorders remains to be established. OBJECTIVE: This paper aims to describe the results of allogeneic hematopoietic stem cell transplantation in patients with advanced indolent lympho...

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Autores principales: Fonseca-Hial, Ana Marcela Rojas, Parisio, Katya, Oliveira, Jose Salvador Rodrigues
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Hematologia e Hemoterapia 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877659/
https://www.ncbi.nlm.nih.gov/pubmed/27208567
http://dx.doi.org/10.1016/j.bjhh.2016.02.006
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author Fonseca-Hial, Ana Marcela Rojas
Parisio, Katya
Oliveira, Jose Salvador Rodrigues
author_facet Fonseca-Hial, Ana Marcela Rojas
Parisio, Katya
Oliveira, Jose Salvador Rodrigues
author_sort Fonseca-Hial, Ana Marcela Rojas
collection PubMed
description BACKGROUND: The role of allogeneic hematopoietic stem cell transplantation for advanced indolent lymphoproliferative disorders remains to be established. OBJECTIVE: This paper aims to describe the results of allogeneic hematopoietic stem cell transplantation in patients with advanced indolent lymphoproliferative disorders. METHODS: This article reports on 29 adult patients submitted to allogeneic transplantations from 1997 to 2010. RESULTS: Most had follicular non-Hodgkin lymphoma (n = 14) or chronic lymphocytic leukemia (n = 12). The median age was 44 years (range: 24–53 years) and 65% of patients were male. Only 21% had had access to rituximab and 45% to fludarabine. All had advanced disease (stage IV) with partial response or stable disease. Most underwent myeloablative conditioning n = 17 – 59%). In this scenario, refractory disease was observed in seven (24%) patients, the 100-day mortality rate was 17% (n = 5) and relapse occurred in four patients (18%). The main cause of death throughout the follow up was refractory disease in six of the 12 patients who died. Moderate and severe chronic graft-versus-host disease was frequent; about 41% of 24 patients analyzed. The overall survival rates and disease free survival at 42 months were 56.7% and 45.4%, respectively. According to Kaplan–Meyer analysis, the median time from diagnosis to transplant predicted the overall survival; however age, gender and conditioning regimen did not predict the prognosis. It was impossible to reach other conclusions because of the small sample size in this study. CONCLUSIONS: The role of allogeneic transplantations should be re-evaluated in the era of targeted therapy.
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spelling pubmed-48776592016-06-09 Allogeneic hematopoietic stem cell transplantation in patients with advanced indolent lymphoproliferative disorders Fonseca-Hial, Ana Marcela Rojas Parisio, Katya Oliveira, Jose Salvador Rodrigues Rev Bras Hematol Hemoter Original Article BACKGROUND: The role of allogeneic hematopoietic stem cell transplantation for advanced indolent lymphoproliferative disorders remains to be established. OBJECTIVE: This paper aims to describe the results of allogeneic hematopoietic stem cell transplantation in patients with advanced indolent lymphoproliferative disorders. METHODS: This article reports on 29 adult patients submitted to allogeneic transplantations from 1997 to 2010. RESULTS: Most had follicular non-Hodgkin lymphoma (n = 14) or chronic lymphocytic leukemia (n = 12). The median age was 44 years (range: 24–53 years) and 65% of patients were male. Only 21% had had access to rituximab and 45% to fludarabine. All had advanced disease (stage IV) with partial response or stable disease. Most underwent myeloablative conditioning n = 17 – 59%). In this scenario, refractory disease was observed in seven (24%) patients, the 100-day mortality rate was 17% (n = 5) and relapse occurred in four patients (18%). The main cause of death throughout the follow up was refractory disease in six of the 12 patients who died. Moderate and severe chronic graft-versus-host disease was frequent; about 41% of 24 patients analyzed. The overall survival rates and disease free survival at 42 months were 56.7% and 45.4%, respectively. According to Kaplan–Meyer analysis, the median time from diagnosis to transplant predicted the overall survival; however age, gender and conditioning regimen did not predict the prognosis. It was impossible to reach other conclusions because of the small sample size in this study. CONCLUSIONS: The role of allogeneic transplantations should be re-evaluated in the era of targeted therapy. Sociedade Brasileira de Hematologia e Hemoterapia 2016 2016-03-19 /pmc/articles/PMC4877659/ /pubmed/27208567 http://dx.doi.org/10.1016/j.bjhh.2016.02.006 Text en © 2016 Associaç˜ao Brasileira de Hematologia, Hemoterapia e Terapia Celular. Published by Elsevier Editora Ltda. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Fonseca-Hial, Ana Marcela Rojas
Parisio, Katya
Oliveira, Jose Salvador Rodrigues
Allogeneic hematopoietic stem cell transplantation in patients with advanced indolent lymphoproliferative disorders
title Allogeneic hematopoietic stem cell transplantation in patients with advanced indolent lymphoproliferative disorders
title_full Allogeneic hematopoietic stem cell transplantation in patients with advanced indolent lymphoproliferative disorders
title_fullStr Allogeneic hematopoietic stem cell transplantation in patients with advanced indolent lymphoproliferative disorders
title_full_unstemmed Allogeneic hematopoietic stem cell transplantation in patients with advanced indolent lymphoproliferative disorders
title_short Allogeneic hematopoietic stem cell transplantation in patients with advanced indolent lymphoproliferative disorders
title_sort allogeneic hematopoietic stem cell transplantation in patients with advanced indolent lymphoproliferative disorders
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877659/
https://www.ncbi.nlm.nih.gov/pubmed/27208567
http://dx.doi.org/10.1016/j.bjhh.2016.02.006
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