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The progress of targeted therapy in advanced gastric cancer
Although palliative chemotherapy has been shown to prolong survival and improve quality of life, the survival of advanced gastric cancer (AGC) patients remains poor. With the advent of targeted therapy, many molecular targeted agents have been evaluated in clinical studies. Trastuzumab, an anti-HER2...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878836/ https://www.ncbi.nlm.nih.gov/pubmed/24330856 http://dx.doi.org/10.1186/2050-7771-1-32 |
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author | Qiu, Miao-zhen Xu, Rui-hua |
author_facet | Qiu, Miao-zhen Xu, Rui-hua |
author_sort | Qiu, Miao-zhen |
collection | PubMed |
description | Although palliative chemotherapy has been shown to prolong survival and improve quality of life, the survival of advanced gastric cancer (AGC) patients remains poor. With the advent of targeted therapy, many molecular targeted agents have been evaluated in clinical studies. Trastuzumab, an anti-HER2 monoclonal antibody, has shown activity against HER2-positive AGC and becomes the first targeted agent approved in AGC. Drugs that target epidermal growth factor receptor, including monoclonal antibody and tyrosine kinase inhibitor, do not bring survival benefit to patients with AGC. Additionally, vascular endothelial growth factor inhibitors are also under investigation. Ramucirumab has shown promising result. Other targeted agents are in preclinical or early clinical development, such as mammalian target of rapamycinm inhibitors and c-MET inhibitors. |
format | Online Article Text |
id | pubmed-3878836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38788362014-01-03 The progress of targeted therapy in advanced gastric cancer Qiu, Miao-zhen Xu, Rui-hua Biomark Res Review Although palliative chemotherapy has been shown to prolong survival and improve quality of life, the survival of advanced gastric cancer (AGC) patients remains poor. With the advent of targeted therapy, many molecular targeted agents have been evaluated in clinical studies. Trastuzumab, an anti-HER2 monoclonal antibody, has shown activity against HER2-positive AGC and becomes the first targeted agent approved in AGC. Drugs that target epidermal growth factor receptor, including monoclonal antibody and tyrosine kinase inhibitor, do not bring survival benefit to patients with AGC. Additionally, vascular endothelial growth factor inhibitors are also under investigation. Ramucirumab has shown promising result. Other targeted agents are in preclinical or early clinical development, such as mammalian target of rapamycinm inhibitors and c-MET inhibitors. BioMed Central 2013-12-11 /pmc/articles/PMC3878836/ /pubmed/24330856 http://dx.doi.org/10.1186/2050-7771-1-32 Text en Copyright © 2013 Qiu and Xu; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Qiu, Miao-zhen Xu, Rui-hua The progress of targeted therapy in advanced gastric cancer |
title | The progress of targeted therapy in advanced gastric cancer |
title_full | The progress of targeted therapy in advanced gastric cancer |
title_fullStr | The progress of targeted therapy in advanced gastric cancer |
title_full_unstemmed | The progress of targeted therapy in advanced gastric cancer |
title_short | The progress of targeted therapy in advanced gastric cancer |
title_sort | progress of targeted therapy in advanced gastric cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878836/ https://www.ncbi.nlm.nih.gov/pubmed/24330856 http://dx.doi.org/10.1186/2050-7771-1-32 |
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