Mechanisms of Acquired Resistance to Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Non–Small Cell Lung Cancer
Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors gefitinib and erlotinib are effective therapies for non–small cell lung cancer patients whose tumors harbor somatic mutations in EGFR . All patients, however, ultimately develop resistance to these agents. Thus, there is a great need...
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Veröffentlicht in: | Clinical cancer research 2008-05, Vol.14 (10), p.2895-2899 |
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creator | Engelman, Jeffrey A. Jänne, Pasi A. |
description | Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors gefitinib and erlotinib are effective therapies for non–small
cell lung cancer patients whose tumors harbor somatic mutations in EGFR . All patients, however, ultimately develop resistance to these agents. Thus, there is a great need to understand how patients
become resistant to develop effective therapies for these cancers. Studies over the last few years have identified two different
EGFR tyrosine kinase inhibitor resistance mechanisms, a secondary mutation in EGFR, EGFR 790M, and amplification of the MET oncogene. These findings have led to clinical trials using newly designed targeted therapies that can overcome these resistance
mechanisms and have shown promise in laboratory studies. Ongoing research efforts will likely continue to identify additional
resistance mechanisms, and these findings will hopefully translate into effective therapies for non–small cell lung cancer
patients. |
doi_str_mv | 10.1158/1078-0432.CCR-07-2248 |
format | Article |
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cell lung cancer patients whose tumors harbor somatic mutations in EGFR . All patients, however, ultimately develop resistance to these agents. Thus, there is a great need to understand how patients
become resistant to develop effective therapies for these cancers. Studies over the last few years have identified two different
EGFR tyrosine kinase inhibitor resistance mechanisms, a secondary mutation in EGFR, EGFR 790M, and amplification of the MET oncogene. These findings have led to clinical trials using newly designed targeted therapies that can overcome these resistance
mechanisms and have shown promise in laboratory studies. Ongoing research efforts will likely continue to identify additional
resistance mechanisms, and these findings will hopefully translate into effective therapies for non–small cell lung cancer
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cell lung cancer patients whose tumors harbor somatic mutations in EGFR . All patients, however, ultimately develop resistance to these agents. Thus, there is a great need to understand how patients
become resistant to develop effective therapies for these cancers. Studies over the last few years have identified two different
EGFR tyrosine kinase inhibitor resistance mechanisms, a secondary mutation in EGFR, EGFR 790M, and amplification of the MET oncogene. These findings have led to clinical trials using newly designed targeted therapies that can overcome these resistance
mechanisms and have shown promise in laboratory studies. Ongoing research efforts will likely continue to identify additional
resistance mechanisms, and these findings will hopefully translate into effective therapies for non–small cell lung cancer
patients.</description><subject>Animals</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Carcinoma</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - enzymology</subject><subject>Clinical Trials as Topic</subject><subject>Drug Resistance, Neoplasm - physiology</subject><subject>Humans</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - enzymology</subject><subject>Mutation</subject><subject>Non–Small Cell lung</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Protein-Tyrosine Kinases - antagonists & inhibitors</subject><subject>Receptor, Epidermal Growth Factor - antagonists & inhibitors</subject><subject>Receptor, Epidermal Growth Factor - drug effects</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkMlqHDEQhkVwiNdHSNDJkEM7Wkeao2m84YkNXs5CI1W7FabVY6kb45vfwW-YJ7HaMyEXqUDfX1X6EPpOyQmlUv-iROmKCM5O6vquIqpiTOgvaI9KqSrOZnKn1P-YXbSf8x9CqKBEfEO7VAvNuZR76O03uNbGkLuM-wafuucxJPD4DnLIg40O8NDjs3XwkDq7whepfxlafG7d0KdCOVhPxcNr6nOIgK9DtBnwVWzDMpSXjEPEN338-_Z-X_IrXEM5FmN8wvXUPR2ir41dZTja3gfo8fzsob6sFrcXV_XponJCiqFSXoG2DSEz4r1WyjWSg_Z02ThvOQg9d04R1rACWeHVUljlmPdsxrWb2zk_QMebvuvUP4-QB9OF7MoyNkI_ZqOIElJxUUC5AV35Uk7QmHUKnU2vhhIzqTeTVjNpNUW9IcpM6kvux3bAuOzA_09tXRfg5wZow1P7Uiwb92kgQQabXGuomEYwPZf8A2FZkPw</recordid><startdate>20080515</startdate><enddate>20080515</enddate><creator>Engelman, Jeffrey A.</creator><creator>Jänne, Pasi A.</creator><general>American Association for Cancer Research</general><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></search><sort><creationdate>20080515</creationdate><title>Mechanisms of Acquired Resistance to Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Non–Small Cell Lung Cancer</title><author>Engelman, Jeffrey A. ; Jänne, Pasi A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c454t-7d7e8af0060dd877cf53e8d1bfcda3e489cc702f28afa4d7b4a7c2dd2638c9a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Carcinoma</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - enzymology</topic><topic>Clinical Trials as Topic</topic><topic>Drug Resistance, Neoplasm - physiology</topic><topic>Humans</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - enzymology</topic><topic>Mutation</topic><topic>Non–Small Cell lung</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Protein-Tyrosine Kinases - antagonists & inhibitors</topic><topic>Receptor, Epidermal Growth Factor - antagonists & inhibitors</topic><topic>Receptor, Epidermal Growth Factor - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Engelman, Jeffrey A.</creatorcontrib><creatorcontrib>Jänne, Pasi A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Engelman, Jeffrey A.</au><au>Jänne, Pasi A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mechanisms of Acquired Resistance to Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Non–Small Cell Lung Cancer</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2008-05-15</date><risdate>2008</risdate><volume>14</volume><issue>10</issue><spage>2895</spage><epage>2899</epage><pages>2895-2899</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors gefitinib and erlotinib are effective therapies for non–small
cell lung cancer patients whose tumors harbor somatic mutations in EGFR . All patients, however, ultimately develop resistance to these agents. Thus, there is a great need to understand how patients
become resistant to develop effective therapies for these cancers. Studies over the last few years have identified two different
EGFR tyrosine kinase inhibitor resistance mechanisms, a secondary mutation in EGFR, EGFR 790M, and amplification of the MET oncogene. These findings have led to clinical trials using newly designed targeted therapies that can overcome these resistance
mechanisms and have shown promise in laboratory studies. Ongoing research efforts will likely continue to identify additional
resistance mechanisms, and these findings will hopefully translate into effective therapies for non–small cell lung cancer
patients.</abstract><cop>United States</cop><pub>American Association for Cancer Research</pub><pmid>18483355</pmid><doi>10.1158/1078-0432.CCR-07-2248</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Animals Antineoplastic Agents - therapeutic use Carcinoma Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - enzymology Clinical Trials as Topic Drug Resistance, Neoplasm - physiology Humans Lung Neoplasms - drug therapy Lung Neoplasms - enzymology Mutation Non–Small Cell lung Protein Kinase Inhibitors - therapeutic use Protein-Tyrosine Kinases - antagonists & inhibitors Receptor, Epidermal Growth Factor - antagonists & inhibitors Receptor, Epidermal Growth Factor - drug effects |
title | Mechanisms of Acquired Resistance to Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Non–Small Cell Lung Cancer |
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