Show simple item record

dc.contributor.authorRanson, Malcolm R
dc.date.accessioned2009-08-19T13:08:20Z
dc.date.available2009-08-19T13:08:20Z
dc.date.issued2004-06-14
dc.identifier.citationEpidermal growth factor receptor tyrosine kinase inhibitors. 2004, 90 (12):2250-5 Br. J. Canceren
dc.identifier.issn0007-0920
dc.identifier.pmid15150574
dc.identifier.doi10.1038/sj.bjc.6601873
dc.identifier.urihttp://hdl.handle.net/10541/77854
dc.description.abstractActivation of the epidermal growth factor receptor (EGFR) has been linked to tumour proliferation, invasion, metastasis and angiogenesis in epithelial tumours. Inhibitors of the EGFR have emerged as promising anticancer agents and two main approaches have been developed, humanised monoclonal antibodies and tyrosine kinase inhibitors. This review discusses the current status of EGFR tyrosine kinase inhibitors (EGFR-TKIs) that have entered clinical development. EGFR-TKIs are generally well tolerated and can sometimes produce impressive tumour regression in patients with advanced non-small-cell lung cancer. However, highly predictive or surrogate markers of activity have not been identified and there remains a need for translational research in their future development.
dc.language.isoenen
dc.subjectLung Canceren
dc.subjectTumour Markersen
dc.subject.meshAntibodies, Monoclonal
dc.subject.meshAntineoplastic Agents
dc.subject.meshCarcinoma, Non-Small-Cell Lung
dc.subject.meshClinical Trials as Topic
dc.subject.meshHumans
dc.subject.meshLung Neoplasms
dc.subject.meshProtein-Tyrosine Kinases
dc.subject.meshReceptor, Epidermal Growth Factor
dc.subject.meshTumor Markers, Biological
dc.titleEpidermal growth factor receptor tyrosine kinase inhibitors.en
dc.typeArticleen
dc.contributor.departmentDepartment of Medical Oncology, University of Manchester, Christie Hospital NHS Trust, Wilmslow Road, Manchester M20 4BX, UK. malcolm.ransom@man.ac.uken
dc.identifier.journalBritish Journal of Canceren
html.description.abstractActivation of the epidermal growth factor receptor (EGFR) has been linked to tumour proliferation, invasion, metastasis and angiogenesis in epithelial tumours. Inhibitors of the EGFR have emerged as promising anticancer agents and two main approaches have been developed, humanised monoclonal antibodies and tyrosine kinase inhibitors. This review discusses the current status of EGFR tyrosine kinase inhibitors (EGFR-TKIs) that have entered clinical development. EGFR-TKIs are generally well tolerated and can sometimes produce impressive tumour regression in patients with advanced non-small-cell lung cancer. However, highly predictive or surrogate markers of activity have not been identified and there remains a need for translational research in their future development.


This item appears in the following Collection(s)

Show simple item record