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Chasing targets for EGFR tyrosine kinase inhibitors in non-small-cell lung cancer: Asian perspectives

DC Field Value Language
dc.contributor.authorKim, Toe-You-
dc.contributor.authorHan, Soe-Won-
dc.contributor.authorBang, Yung-Jue-
dc.date.accessioned2021-01-31T11:09:58Z-
dc.date.available2021-01-31T11:09:58Z-
dc.date.created2020-12-23-
dc.date.issued2007-11-
dc.identifier.citationExpert Review of Molecular Diagnostics, Vol.7 No.6, pp.821-836-
dc.identifier.issn1473-7159-
dc.identifier.other119574-
dc.identifier.urihttps://hdl.handle.net/10371/173072-
dc.description.abstractEGF receptor (EGFR) activation has an important role in various steps of carcinogenesis and progression of non-small-cell lung cancer (NSCLC), implying that EGFR is a potential target for cancer therapy. Therefore, targeted treatments aimed at EGFR have been developed, of which tyrosine kinase inhibitors (TKls), gefitinib and erlotinib have shown activity in NSCLC. The unexpected findings of a lack of association between expression of EGFR, the target and efficacy of EGFR TKls and higher response in selective subgroups of patients were puzzling. Identification of somatic activating mutations in the EGFR tyrosine kinase domain solved the mystery and provided new insight. Several lines of study provided information on various molecular targets for EGFR TKl therapy. A target-based patient-selection strategy is expected to eventually lead to tailored therapy for lung cancer.-
dc.language영어-
dc.publisherFuture Drugs Ltd.-
dc.titleChasing targets for EGFR tyrosine kinase inhibitors in non-small-cell lung cancer: Asian perspectives-
dc.typeArticle-
dc.contributor.AlternativeAuthor방영주-
dc.identifier.doi10.1586/14737159.7.6.821-
dc.citation.journaltitleExpert Review of Molecular Diagnostics-
dc.identifier.wosid000251520800013-
dc.identifier.scopusid2-s2.0-36448978322-
dc.citation.endpage836-
dc.citation.number6-
dc.citation.startpage821-
dc.citation.volume7-
dc.identifier.sci000251520800013-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorKim, Toe-You-
dc.contributor.affiliatedAuthorBang, Yung-Jue-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.subject.keywordPlusGROWTH-FACTOR-RECEPTOR-
dc.subject.keywordPlusGENE COPY NUMBER-
dc.subject.keywordPlusPREVIOUSLY TREATED PATIENTS-
dc.subject.keywordPlusMETASTATIC BREAST-CANCER-
dc.subject.keywordPlusPHASE-II TRIAL-
dc.subject.keywordPlusDOMAIN MUTATIONS-
dc.subject.keywordPlusACQUIRED-RESISTANCE-
dc.subject.keywordPlusPROTEIN EXPRESSION-
dc.subject.keywordPlusSOMATIC MUTATIONS-
dc.subject.keywordPlusJAPANESE PATIENTS-
dc.subject.keywordAuthoramplification-
dc.subject.keywordAuthorbiomarker-
dc.subject.keywordAuthorEGFR-
dc.subject.keywordAuthorerlotinib-
dc.subject.keywordAuthorFISH-
dc.subject.keywordAuthorgefitinib-
dc.subject.keywordAuthormutation-
dc.subject.keywordAuthorNSCLC-
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  • College of Medicine
  • Department of Medicine
Research Area Clinical Medicine

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