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Recombinant human endostatin in combination with CHOP regimen for peripheral T cell lymphoma
Peripheral T cell lymphoma (PTCL) has a poor prognosis. Overexpression of vascular endothelial growth factor (VEGF) might contribute to the poor prognosis of PTCL and could be the target of novel therapy. The efficacy and safety of recombinant human endostatin (Endostar) in combination with cyclopho...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5189703/ https://www.ncbi.nlm.nih.gov/pubmed/28053548 http://dx.doi.org/10.2147/OTT.S117007 |
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author | Zhang, Qunling Cao, Junning Xue, Kai Liu, Xiaojian Ji, Dongmei Guo, Ye Hong, Xiaonan |
author_facet | Zhang, Qunling Cao, Junning Xue, Kai Liu, Xiaojian Ji, Dongmei Guo, Ye Hong, Xiaonan |
author_sort | Zhang, Qunling |
collection | PubMed |
description | Peripheral T cell lymphoma (PTCL) has a poor prognosis. Overexpression of vascular endothelial growth factor (VEGF) might contribute to the poor prognosis of PTCL and could be the target of novel therapy. The efficacy and safety of recombinant human endostatin (Endostar) in combination with cyclophosphamide, doxorubicin, vincristine and prednisone (ECHOP) have been explored in 15 PTCL patients. The objective response rate was 80%, with 53.3% patients having achieved complete response (CR) rate. The CR rate was 100% (3/3) in angioimmunoblastic T cell lymphoma (AITL) patients compared to only 36.4% (4/11) in PTCL not otherwise specified (PTCL-NOS) patients. With a median follow-up of 69 months, the 5-year progression-free survival and overall survival (OS) were 53% and 60%, respectively. The 5-year OS was 100% in AITL but was only 45% in PTCL-NOS. Seven out of 11 patients showed overexpression of VEGFR2 in their tumor vessels and had a better efficacy than those with low expression of VEGFR2. Grade 3 or 4 neutropenia is the most common toxicity observed. ECHOP was safe and might display potential benefit in AITL patients. |
format | Online Article Text |
id | pubmed-5189703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-51897032017-01-04 Recombinant human endostatin in combination with CHOP regimen for peripheral T cell lymphoma Zhang, Qunling Cao, Junning Xue, Kai Liu, Xiaojian Ji, Dongmei Guo, Ye Hong, Xiaonan Onco Targets Ther Clinical Trial Report Peripheral T cell lymphoma (PTCL) has a poor prognosis. Overexpression of vascular endothelial growth factor (VEGF) might contribute to the poor prognosis of PTCL and could be the target of novel therapy. The efficacy and safety of recombinant human endostatin (Endostar) in combination with cyclophosphamide, doxorubicin, vincristine and prednisone (ECHOP) have been explored in 15 PTCL patients. The objective response rate was 80%, with 53.3% patients having achieved complete response (CR) rate. The CR rate was 100% (3/3) in angioimmunoblastic T cell lymphoma (AITL) patients compared to only 36.4% (4/11) in PTCL not otherwise specified (PTCL-NOS) patients. With a median follow-up of 69 months, the 5-year progression-free survival and overall survival (OS) were 53% and 60%, respectively. The 5-year OS was 100% in AITL but was only 45% in PTCL-NOS. Seven out of 11 patients showed overexpression of VEGFR2 in their tumor vessels and had a better efficacy than those with low expression of VEGFR2. Grade 3 or 4 neutropenia is the most common toxicity observed. ECHOP was safe and might display potential benefit in AITL patients. Dove Medical Press 2016-12-22 /pmc/articles/PMC5189703/ /pubmed/28053548 http://dx.doi.org/10.2147/OTT.S117007 Text en © 2017 Zhang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Clinical Trial Report Zhang, Qunling Cao, Junning Xue, Kai Liu, Xiaojian Ji, Dongmei Guo, Ye Hong, Xiaonan Recombinant human endostatin in combination with CHOP regimen for peripheral T cell lymphoma |
title | Recombinant human endostatin in combination with CHOP regimen for peripheral T cell lymphoma |
title_full | Recombinant human endostatin in combination with CHOP regimen for peripheral T cell lymphoma |
title_fullStr | Recombinant human endostatin in combination with CHOP regimen for peripheral T cell lymphoma |
title_full_unstemmed | Recombinant human endostatin in combination with CHOP regimen for peripheral T cell lymphoma |
title_short | Recombinant human endostatin in combination with CHOP regimen for peripheral T cell lymphoma |
title_sort | recombinant human endostatin in combination with chop regimen for peripheral t cell lymphoma |
topic | Clinical Trial Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5189703/ https://www.ncbi.nlm.nih.gov/pubmed/28053548 http://dx.doi.org/10.2147/OTT.S117007 |
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