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Erlotinib in the treatment of advanced pancreatic cancer

Single agent gemcitabine has been the mainstay of therapy for advanced pancreatic cancer over the past decade. Multiple trials of newer chemotherapeutic agents both alone and in combination have yielded disappointing results, spurring the ongoing search for new agents and combinations in this aggres...

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Detalles Bibliográficos
Autores principales: Kelley, Robin K, Ko, Andrew H
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2727779/
https://www.ncbi.nlm.nih.gov/pubmed/19707431
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author Kelley, Robin K
Ko, Andrew H
author_facet Kelley, Robin K
Ko, Andrew H
author_sort Kelley, Robin K
collection PubMed
description Single agent gemcitabine has been the mainstay of therapy for advanced pancreatic cancer over the past decade. Multiple trials of newer chemotherapeutic agents both alone and in combination have yielded disappointing results, spurring the ongoing search for new agents and combinations in this aggressive malignancy. Inhibitors of the epidermal growth factor receptor (EGFR) have shown promising activity in multiple solid tumors types, and preclinical data support a role for EGFR inhibition in pancreatic cancer. A recent phase III study by the National Cancer Institute of Canada Clinical Trials Group (NCIC-CTG) demonstrated a significant survival benefit with the addition of the EGFR tyrosine kinase inhibitor, erlotinib, to gemcitabine chemotherapy for the first-line treatment of patients with advanced pancreatic cancer, becoming the first phase III study to demonstrate a survival benefit of combination therapy as well as targeted therapy in this disease. This article reviews the evidence supporting EGFR inhibition and the use of erlotinib in advanced pancreatic cancer as well as future implications of targeted therapy in this challenging malignancy.
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spelling pubmed-27277792009-08-25 Erlotinib in the treatment of advanced pancreatic cancer Kelley, Robin K Ko, Andrew H Biologics Review Single agent gemcitabine has been the mainstay of therapy for advanced pancreatic cancer over the past decade. Multiple trials of newer chemotherapeutic agents both alone and in combination have yielded disappointing results, spurring the ongoing search for new agents and combinations in this aggressive malignancy. Inhibitors of the epidermal growth factor receptor (EGFR) have shown promising activity in multiple solid tumors types, and preclinical data support a role for EGFR inhibition in pancreatic cancer. A recent phase III study by the National Cancer Institute of Canada Clinical Trials Group (NCIC-CTG) demonstrated a significant survival benefit with the addition of the EGFR tyrosine kinase inhibitor, erlotinib, to gemcitabine chemotherapy for the first-line treatment of patients with advanced pancreatic cancer, becoming the first phase III study to demonstrate a survival benefit of combination therapy as well as targeted therapy in this disease. This article reviews the evidence supporting EGFR inhibition and the use of erlotinib in advanced pancreatic cancer as well as future implications of targeted therapy in this challenging malignancy. Dove Medical Press 2008-03 2008-03 /pmc/articles/PMC2727779/ /pubmed/19707431 Text en © 2008 Dove Medical Press Limited. All rights reserved
spellingShingle Review
Kelley, Robin K
Ko, Andrew H
Erlotinib in the treatment of advanced pancreatic cancer
title Erlotinib in the treatment of advanced pancreatic cancer
title_full Erlotinib in the treatment of advanced pancreatic cancer
title_fullStr Erlotinib in the treatment of advanced pancreatic cancer
title_full_unstemmed Erlotinib in the treatment of advanced pancreatic cancer
title_short Erlotinib in the treatment of advanced pancreatic cancer
title_sort erlotinib in the treatment of advanced pancreatic cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2727779/
https://www.ncbi.nlm.nih.gov/pubmed/19707431
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