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Autologous stem cell transplantation as frontline strategy for peripheral T-cell lymphoma: A single-centre experience
OBJECTIVE: To determine the efficacy and prognosis of autologous hematopoietic stem cell transplantation (ASCT) as frontline treatment for peripheral T cell lymphoma (PTCL). METHODS: Clinical data from 46 PTCL patients who achieved complete (CR) or partial remission (PR) after ASCT from October 1996...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536587/ https://www.ncbi.nlm.nih.gov/pubmed/28222648 http://dx.doi.org/10.1177/0300060516676725 |
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author | Han, Xiao Zhang, Wei Zhou, Daobin Ruan, Jing Duan, Minghui Zhu, Tienan Li, Jian Cai, Huacong Cao, Xinxin Ouyang, Mingqi |
author_facet | Han, Xiao Zhang, Wei Zhou, Daobin Ruan, Jing Duan, Minghui Zhu, Tienan Li, Jian Cai, Huacong Cao, Xinxin Ouyang, Mingqi |
author_sort | Han, Xiao |
collection | PubMed |
description | OBJECTIVE: To determine the efficacy and prognosis of autologous hematopoietic stem cell transplantation (ASCT) as frontline treatment for peripheral T cell lymphoma (PTCL). METHODS: Clinical data from 46 PTCL patients who achieved complete (CR) or partial remission (PR) after ASCT from October 1996 to July 2014 were analysed retrospectively. RESULTS: Median patient age was 32 (range: 15–68) years. Disease types included PTCL, unspecified type, in 23 patients, anaplastic large cell lymphoma in eight, angioimmunoblastic lymphoma in eight, extranodal NK/T-cell lymphoma in five, and hepatosplenic T-cell lymphoma and enteropathy associated T-cell lymphoma in one each. Of these patients, 80% had Prognostic Index for Peripheral T-cell Lymphoma scores ≥1. Thirty-four patients had pre-transplantation CR and 12 had PR. Median follow up was 37 (6–176) months. The 5-year overall survival (OS) and progression-free survival (PFS) rates were 77.1% and 61.9%, respectively. Multivariate analysis showed that pre-transplantation CR was an independent risk factor for survival, and CR was more common than PR (OS 81% vs 59.3%; PFS 71.8% vs 17.8%). CONCLUSION: Frontline consolidation treatment with ASCT was associated with favourable outcomes in patients with PTCL. Pre-transplantation CR was a prognostic factor for survival, suggesting that ASCT may be favoured as front-line consolidation therapy after first complete remission. |
format | Online Article Text |
id | pubmed-5536587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-55365872017-10-03 Autologous stem cell transplantation as frontline strategy for peripheral T-cell lymphoma: A single-centre experience Han, Xiao Zhang, Wei Zhou, Daobin Ruan, Jing Duan, Minghui Zhu, Tienan Li, Jian Cai, Huacong Cao, Xinxin Ouyang, Mingqi J Int Med Res Clinical Reports OBJECTIVE: To determine the efficacy and prognosis of autologous hematopoietic stem cell transplantation (ASCT) as frontline treatment for peripheral T cell lymphoma (PTCL). METHODS: Clinical data from 46 PTCL patients who achieved complete (CR) or partial remission (PR) after ASCT from October 1996 to July 2014 were analysed retrospectively. RESULTS: Median patient age was 32 (range: 15–68) years. Disease types included PTCL, unspecified type, in 23 patients, anaplastic large cell lymphoma in eight, angioimmunoblastic lymphoma in eight, extranodal NK/T-cell lymphoma in five, and hepatosplenic T-cell lymphoma and enteropathy associated T-cell lymphoma in one each. Of these patients, 80% had Prognostic Index for Peripheral T-cell Lymphoma scores ≥1. Thirty-four patients had pre-transplantation CR and 12 had PR. Median follow up was 37 (6–176) months. The 5-year overall survival (OS) and progression-free survival (PFS) rates were 77.1% and 61.9%, respectively. Multivariate analysis showed that pre-transplantation CR was an independent risk factor for survival, and CR was more common than PR (OS 81% vs 59.3%; PFS 71.8% vs 17.8%). CONCLUSION: Frontline consolidation treatment with ASCT was associated with favourable outcomes in patients with PTCL. Pre-transplantation CR was a prognostic factor for survival, suggesting that ASCT may be favoured as front-line consolidation therapy after first complete remission. SAGE Publications 2017-01-12 2017-02 /pmc/articles/PMC5536587/ /pubmed/28222648 http://dx.doi.org/10.1177/0300060516676725 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Clinical Reports Han, Xiao Zhang, Wei Zhou, Daobin Ruan, Jing Duan, Minghui Zhu, Tienan Li, Jian Cai, Huacong Cao, Xinxin Ouyang, Mingqi Autologous stem cell transplantation as frontline strategy for peripheral T-cell lymphoma: A single-centre experience |
title | Autologous stem cell transplantation as frontline strategy for peripheral T-cell lymphoma: A single-centre experience |
title_full | Autologous stem cell transplantation as frontline strategy for peripheral T-cell lymphoma: A single-centre experience |
title_fullStr | Autologous stem cell transplantation as frontline strategy for peripheral T-cell lymphoma: A single-centre experience |
title_full_unstemmed | Autologous stem cell transplantation as frontline strategy for peripheral T-cell lymphoma: A single-centre experience |
title_short | Autologous stem cell transplantation as frontline strategy for peripheral T-cell lymphoma: A single-centre experience |
title_sort | autologous stem cell transplantation as frontline strategy for peripheral t-cell lymphoma: a single-centre experience |
topic | Clinical Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536587/ https://www.ncbi.nlm.nih.gov/pubmed/28222648 http://dx.doi.org/10.1177/0300060516676725 |
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