{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,30]],"date-time":"2025-10-30T07:04:23Z","timestamp":1761807863786},"reference-count":21,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2014,6,19]],"date-time":"2014-06-19T00:00:00Z","timestamp":1403136000000},"content-version":"vor","delay-in-days":18,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"AstraZeneca"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Internal Medicine Journal"],"published-print":{"date-parts":[[2014,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Molecular characterisation of non\u2010squamous non\u2010small\u2010cell lung cancer (<jats:styled-content style=\"fixed-case\">NSCLC<\/jats:styled-content>) is required to direct optimal treatment. Treatment of <jats:styled-content style=\"fixed-case\">NSCLC<\/jats:styled-content> with inhibitors of epidermal growth factor receptor (<jats:styled-content style=\"fixed-case\">EGFR<\/jats:styled-content>) tyrosine kinase (<jats:styled-content style=\"fixed-case\">EGFR\u2010TKI<\/jats:styled-content>) should be guided by the presence of activating mutations of the <jats:styled-content style=\"fixed-case\">EGFR<\/jats:styled-content> gene.<\/jats:p><\/jats:sec><jats:sec><jats:title>Aim<\/jats:title><jats:p>To gain insight into the rate of testing, the range of tissues samples, test utility and outcome when cost of testing as a barrier to access is removed in the <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>ustralian setting.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>In <jats:styled-content style=\"fixed-case\">October<\/jats:styled-content> 2010, a sponsored programme was commenced to gather data on <jats:styled-content style=\"fixed-case\">EGFR<\/jats:styled-content> gene mutation testing in <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>ustralia. Partnering laboratories were funded for provision of de\u2010identified results. For participating patients, the programme supported the test charge. Mutation testing was performed using <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>anger sequencing of exons 18\u201321 of the <jats:styled-content style=\"fixed-case\">EGFR<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Samples 2013 were submitted from 2012 patients. Full sequencing was achieved in 1717 (85%). Failure of full sequencing was more likely in samples derived from fine needle aspiration(<jats:styled-content style=\"fixed-case\">FNA<\/jats:styled-content>) biopsy than tissue biopsy or pleural\/pericardial fluid cell blocks <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content> 3.1 (95% CI 1.9\u20135.2). There were 359 mutations seen in 337 patients. 14.5% of cases had a classical mutation conferring sensitivity to <jats:styled-content style=\"fixed-case\">EGFR\u2010TKI<\/jats:styled-content>. In addition there was a range of less common mutations \u2013 some predicting responses and others of uncertain significance. 1.4% of cases had mutations associated with non\u2010responsiveness to <jats:styled-content style=\"fixed-case\">EGFR\u2010TKI<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">EGFR<\/jats:styled-content> gene mutation testing is feasible on local and interstate lung cancer samples. The rate of valid test outcomes is high, but <jats:styled-content style=\"fixed-case\">FNA<\/jats:styled-content> samples are associated with more frequent test failure.<\/jats:p><\/jats:sec>","DOI":"10.1111\/imj.12449","type":"journal-article","created":{"date-parts":[[2014,4,10]],"date-time":"2014-04-10T18:19:15Z","timestamp":1397153955000},"page":"575-580","update-policy":"http:\/\/dx.doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":7,"title":["Outcomes of an <scp>A<\/scp>ustralian testing programme for epidermal growth factor receptor mutations in non\u2010small cell lung cancer"],"prefix":"10.1111","volume":"44","author":[{"given":"M. J.","family":"Peters","sequence":"first","affiliation":[{"name":"Concord Repatriation General Hospital  Sydney New South Wales Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J. 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