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Metastatic gastric cancer – focus on targeted therapies

Gastric cancer (GC) is currently the second leading cause of cancer death worldwide; unfortunately, most patients will present with locally advanced or metastatic disease. Despite recent progress in diagnosis, surgery, chemotherapy, and radiotherapy, prognosis remains poor. A better understanding of...

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Detalles Bibliográficos
Autores principales: Meza-Junco, Judith, Sawyer, Michael B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395896/
https://www.ncbi.nlm.nih.gov/pubmed/22807624
http://dx.doi.org/10.2147/BTT.S23917
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author Meza-Junco, Judith
Sawyer, Michael B
author_facet Meza-Junco, Judith
Sawyer, Michael B
author_sort Meza-Junco, Judith
collection PubMed
description Gastric cancer (GC) is currently the second leading cause of cancer death worldwide; unfortunately, most patients will present with locally advanced or metastatic disease. Despite recent progress in diagnosis, surgery, chemotherapy, and radiotherapy, prognosis remains poor. A better understanding of GC biology and signaling pathways is expected to improve GC therapy, and the integration of targeted therapies has recently become possible and appears to be promising. This article focuses on anti-Her-2 therapy, specifically trastuzumab, as well as other epidermal growth factor receptor antagonists such as cetuximab, panitumub, matuzumab, nimotzumab, gefitinib, and erlotinib. Additionally, drugs that target angiogenesis pathways are also under investigation, particulary bevacizumab, ramucirumab, sorafenib, sunitinib, and cediranib. Other targeted agents in preclinical or early clinical development include mTOR inhibitors, anti c-MET, polo-like kinase 1 inhibitors, anti-insulin-like growth factor, anti-heat shock proteins, and small molecules targeting Hedgehog signaling.
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spelling pubmed-33958962012-07-17 Metastatic gastric cancer – focus on targeted therapies Meza-Junco, Judith Sawyer, Michael B Biologics Review Gastric cancer (GC) is currently the second leading cause of cancer death worldwide; unfortunately, most patients will present with locally advanced or metastatic disease. Despite recent progress in diagnosis, surgery, chemotherapy, and radiotherapy, prognosis remains poor. A better understanding of GC biology and signaling pathways is expected to improve GC therapy, and the integration of targeted therapies has recently become possible and appears to be promising. This article focuses on anti-Her-2 therapy, specifically trastuzumab, as well as other epidermal growth factor receptor antagonists such as cetuximab, panitumub, matuzumab, nimotzumab, gefitinib, and erlotinib. Additionally, drugs that target angiogenesis pathways are also under investigation, particulary bevacizumab, ramucirumab, sorafenib, sunitinib, and cediranib. Other targeted agents in preclinical or early clinical development include mTOR inhibitors, anti c-MET, polo-like kinase 1 inhibitors, anti-insulin-like growth factor, anti-heat shock proteins, and small molecules targeting Hedgehog signaling. Dove Medical Press 2012 2012-06-20 /pmc/articles/PMC3395896/ /pubmed/22807624 http://dx.doi.org/10.2147/BTT.S23917 Text en © 2012 Meza-Junco and Sawyer, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Meza-Junco, Judith
Sawyer, Michael B
Metastatic gastric cancer – focus on targeted therapies
title Metastatic gastric cancer – focus on targeted therapies
title_full Metastatic gastric cancer – focus on targeted therapies
title_fullStr Metastatic gastric cancer – focus on targeted therapies
title_full_unstemmed Metastatic gastric cancer – focus on targeted therapies
title_short Metastatic gastric cancer – focus on targeted therapies
title_sort metastatic gastric cancer – focus on targeted therapies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395896/
https://www.ncbi.nlm.nih.gov/pubmed/22807624
http://dx.doi.org/10.2147/BTT.S23917
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