Translational research in pancreatic ductal adenocarcinoma: current evidence and future concepts
Pancreatic ductal adenocarcinoma(PDA) is one of the major causes for cancer death worldwide. Treatment of metastatic disease remains challenging as only certain patients benefit from advances made with the intensified chemotherapy regimen folinic acid, irinotecan and oxaliplatin, the epidermal growt...
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Veröffentlicht in: | World journal of gastroenterology : WJG 2014-08, Vol.20 (31), p.10769-10777 |
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creator | Kruger, Stephan Haas, Michael Ormanns, Steffen Bächmann, Sibylle Siveke, Jens T Kirchner, Thomas Heinemann, Volker Boeck, Stefan |
description | Pancreatic ductal adenocarcinoma(PDA) is one of the major causes for cancer death worldwide. Treatment of metastatic disease remains challenging as only certain patients benefit from advances made with the intensified chemotherapy regimen folinic acid, irinotecan and oxaliplatin, the epidermal growth factor receptor inhibitor erlotinib or the recently FDA-approved nab-paclitaxel. Up to date, no established approach for prediction of treatment response or specific treatment allocation exists. Translational research was able to identify a number of potential biomarkers that might help to improve the dismal prognosis of PDA by facilitating upfront treatment allocation. This topic highlight is focused on current evidence on potential biomarkers for tumor biology, prognosis and prediction of treatment efficacy. |
doi_str_mv | 10.3748/wjg.v20.i31.10769 |
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Treatment of metastatic disease remains challenging as only certain patients benefit from advances made with the intensified chemotherapy regimen folinic acid, irinotecan and oxaliplatin, the epidermal growth factor receptor inhibitor erlotinib or the recently FDA-approved nab-paclitaxel. Up to date, no established approach for prediction of treatment response or specific treatment allocation exists. Translational research was able to identify a number of potential biomarkers that might help to improve the dismal prognosis of PDA by facilitating upfront treatment allocation. This topic highlight is focused on current evidence on potential biomarkers for tumor biology, prognosis and prediction of treatment efficacy.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v20.i31.10769</identifier><identifier>PMID: 25152580</identifier><language>eng</language><publisher>United States: Baishideng Publishing Group Inc</publisher><subject>Animals ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biomarker ; Biomarkers, Tumor - genetics ; Biomarkers, Tumor - metabolism ; Carcinoma, Pancreatic Ductal - drug therapy ; Carcinoma, Pancreatic Ductal - genetics ; Carcinoma, Pancreatic Ductal - metabolism ; Carcinoma, Pancreatic Ductal - pathology ; equilibrativ ; Erlotinib ; Gemcitabine ; Human ; Humans ; Molecular Targeted Therapy ; Pancreatic Neoplasms - drug therapy ; Pancreatic Neoplasms - genetics ; Pancreatic Neoplasms - metabolism ; Pancreatic Neoplasms - pathology ; Precision Medicine ; Predictive Value of Tests ; Signal Transduction ; Topic Highlight ; Translational Research, Biomedical</subject><ispartof>World journal of gastroenterology : WJG, 2014-08, Vol.20 (31), p.10769-10777</ispartof><rights>2014 Baishideng Publishing Group Inc. 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Treatment of metastatic disease remains challenging as only certain patients benefit from advances made with the intensified chemotherapy regimen folinic acid, irinotecan and oxaliplatin, the epidermal growth factor receptor inhibitor erlotinib or the recently FDA-approved nab-paclitaxel. Up to date, no established approach for prediction of treatment response or specific treatment allocation exists. Translational research was able to identify a number of potential biomarkers that might help to improve the dismal prognosis of PDA by facilitating upfront treatment allocation. This topic highlight is focused on current evidence on potential biomarkers for tumor biology, prognosis and prediction of treatment efficacy.</description><subject>Animals</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biomarker</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Carcinoma, Pancreatic Ductal - drug therapy</subject><subject>Carcinoma, Pancreatic Ductal - genetics</subject><subject>Carcinoma, Pancreatic Ductal - metabolism</subject><subject>Carcinoma, Pancreatic Ductal - pathology</subject><subject>equilibrativ</subject><subject>Erlotinib</subject><subject>Gemcitabine</subject><subject>Human</subject><subject>Humans</subject><subject>Molecular Targeted Therapy</subject><subject>Pancreatic Neoplasms - drug therapy</subject><subject>Pancreatic Neoplasms - genetics</subject><subject>Pancreatic Neoplasms - metabolism</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Precision Medicine</subject><subject>Predictive Value of Tests</subject><subject>Signal Transduction</subject><subject>Topic Highlight</subject><subject>Translational Research, Biomedical</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkUFvEzEQhS0EomnhB3BBe-SyYcZj73o5IKGqLUiVeiln43i9iauNndq7Qfx7nDZEdC4e-b15M9LH2AeEJbVCff79sF7uOSw94RKhbbpXbME5djVXAl6zBQK0dUe8PWPnOT8AcCLJ37IzLlFyqWDBft0nE_JoJh-DGavksjPJbiofqp0JNrmi2Kqf7VRU07sQbdF9iFvzpbJzSi5Mldv7olhXmdBXwzzNyVU2lo_dlN-xN4MZs3t_fC_Yz-ur-8vv9e3dzY_Lb7e1FYKmGlW7atFgsxpaoKFRvOmbvuWWryQKLhRIRUggLSJJYXoyjZXSkCBHxrV0wb4-5-7m1db1ttyVzKh3yW9N-qOj8fqlEvxGr-NeCyQl5CHg0zEgxcfZ5UlvfbZuHE1wcc4aG-gIFGBTrPhstSnmnNxwWoOgD2R0IaMLGV3I6CcyZebj__edJv6hKAY6hm5iWD_6sD55OlCH6iQIJbpiR9E9dUB_AR5Nm9o</recordid><startdate>20140821</startdate><enddate>20140821</enddate><creator>Kruger, Stephan</creator><creator>Haas, Michael</creator><creator>Ormanns, Steffen</creator><creator>Bächmann, Sibylle</creator><creator>Siveke, Jens T</creator><creator>Kirchner, Thomas</creator><creator>Heinemann, Volker</creator><creator>Boeck, Stefan</creator><general>Baishideng Publishing Group Inc</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140821</creationdate><title>Translational research in pancreatic ductal adenocarcinoma: current evidence and future concepts</title><author>Kruger, Stephan ; 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subjects | Animals Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biomarker Biomarkers, Tumor - genetics Biomarkers, Tumor - metabolism Carcinoma, Pancreatic Ductal - drug therapy Carcinoma, Pancreatic Ductal - genetics Carcinoma, Pancreatic Ductal - metabolism Carcinoma, Pancreatic Ductal - pathology equilibrativ Erlotinib Gemcitabine Human Humans Molecular Targeted Therapy Pancreatic Neoplasms - drug therapy Pancreatic Neoplasms - genetics Pancreatic Neoplasms - metabolism Pancreatic Neoplasms - pathology Precision Medicine Predictive Value of Tests Signal Transduction Topic Highlight Translational Research, Biomedical |
title | Translational research in pancreatic ductal adenocarcinoma: current evidence and future concepts |
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