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Targeted and novel therapy in advanced gastric cancer
The systemic treatment options for advanced gastric cancer (GC) have evolved rapidly in recent years. We have reviewed the recent data of clinical trial incorporating targeted agents, including inhibitors of angiogenesis, human epidermal growth factor receptor 2 (HER2), mesenchymal–epithelial transi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788003/ https://www.ncbi.nlm.nih.gov/pubmed/31632839 http://dx.doi.org/10.1186/s40164-019-0149-6 |
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author | Selim, Julie H. Shaheen, Shagufta Sheu, Wei-Chun Hsueh, Chung-Tsen |
author_facet | Selim, Julie H. Shaheen, Shagufta Sheu, Wei-Chun Hsueh, Chung-Tsen |
author_sort | Selim, Julie H. |
collection | PubMed |
description | The systemic treatment options for advanced gastric cancer (GC) have evolved rapidly in recent years. We have reviewed the recent data of clinical trial incorporating targeted agents, including inhibitors of angiogenesis, human epidermal growth factor receptor 2 (HER2), mesenchymal–epithelial transition, epidermal growth factor receptor, mammalian target of rapamycin, claudin-18.2, programmed death-1 and DNA. Addition of trastuzumab to platinum-based chemotherapy has become standard of care as front-line therapy in advanced GC overexpressing HER2. In the second-line setting, ramucirumab with paclitaxel significantly improves overall survival compared to paclitaxel alone. For patients with refractory disease, apatinib, nivolumab, ramucirumab and TAS-102 have demonstrated single-agent activity with improved overall survival compared to placebo alone. Pembrolizumab has demonstrated more than 50% response rate in microsatellite instability-high tumors, 15% response rate in tumors expressing programmed death ligand 1, and non-inferior outcome in first-line treatment compared to chemotherapy. This review summarizes the current state and progress of research on targeted therapy for advanced GC. |
format | Online Article Text |
id | pubmed-6788003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67880032019-10-18 Targeted and novel therapy in advanced gastric cancer Selim, Julie H. Shaheen, Shagufta Sheu, Wei-Chun Hsueh, Chung-Tsen Exp Hematol Oncol Review The systemic treatment options for advanced gastric cancer (GC) have evolved rapidly in recent years. We have reviewed the recent data of clinical trial incorporating targeted agents, including inhibitors of angiogenesis, human epidermal growth factor receptor 2 (HER2), mesenchymal–epithelial transition, epidermal growth factor receptor, mammalian target of rapamycin, claudin-18.2, programmed death-1 and DNA. Addition of trastuzumab to platinum-based chemotherapy has become standard of care as front-line therapy in advanced GC overexpressing HER2. In the second-line setting, ramucirumab with paclitaxel significantly improves overall survival compared to paclitaxel alone. For patients with refractory disease, apatinib, nivolumab, ramucirumab and TAS-102 have demonstrated single-agent activity with improved overall survival compared to placebo alone. Pembrolizumab has demonstrated more than 50% response rate in microsatellite instability-high tumors, 15% response rate in tumors expressing programmed death ligand 1, and non-inferior outcome in first-line treatment compared to chemotherapy. This review summarizes the current state and progress of research on targeted therapy for advanced GC. BioMed Central 2019-10-11 /pmc/articles/PMC6788003/ /pubmed/31632839 http://dx.doi.org/10.1186/s40164-019-0149-6 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Selim, Julie H. Shaheen, Shagufta Sheu, Wei-Chun Hsueh, Chung-Tsen Targeted and novel therapy in advanced gastric cancer |
title | Targeted and novel therapy in advanced gastric cancer |
title_full | Targeted and novel therapy in advanced gastric cancer |
title_fullStr | Targeted and novel therapy in advanced gastric cancer |
title_full_unstemmed | Targeted and novel therapy in advanced gastric cancer |
title_short | Targeted and novel therapy in advanced gastric cancer |
title_sort | targeted and novel therapy in advanced gastric cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788003/ https://www.ncbi.nlm.nih.gov/pubmed/31632839 http://dx.doi.org/10.1186/s40164-019-0149-6 |
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