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Mutasjonstesting ved ikke-småcellet lungekreft
Engelsk titel: Mutation testing for non-small-cell lung cancer Läs online Författare: Brustugun, Odd Terje ; Helland, Åslaug ; Fjellbirkeland, Lars ; Kleinberg, Lilach ; Ariansen, Sarah ; Jbsen, Peter ; Scott, Helge ; Dönnem, Roy ; Bremnes, Roy ; Berg, Thomas ; Grönberg, Björn Henning ; Dai, Hong Yan ; Wahl, Sissel Gyrid Freim ; Mangseth, Kjersti ; Helgeland, Lars Språk: Nor Antal referenser: 20 Dokumenttyp: Artikel UI-nummer: 12051935

Tidskrift

Tidsskrift for Den Norske Laegeforening 2012;132(8)952-5 ISSN 0029-2001 E-ISSN 0807-7096 KIBs bestånd av denna tidskrift Denna tidskrift är expertgranskad (Peer-Reviewed)

Sammanfattning

Background. Epidermal growth-factor receptor (EGFR) tyrosine kinase inhibitors (EGFR-TKI) are a relatively new class of drugs for treatment of non-small-cell lung cancer. The national professional group for lung cancer, The Norwegian Lung Cancer Group, recommends that patients with non-small-cell lung cancer are tested for mutations in the EGFR gene. Here, we report the experience collected after the introduction of such testing in Norway in 2010. Material and method. Information on the number of patients tested, gender distribution, histopathological data and analysis results have been collected from the molecular-pathology laboratories at the university hospitals in Tromsø, Trondheim, Bergen and Oslo for the period from May 2010 to May 2011. Results. During this period, altogether 1 058 patients with lung cancer were tested for mutations in the EGFR gene, equal to approximately half of all those who were diagnosed with non-small-cell lung cancer. A mutation was detected in 123 patients (11.6 per cent). There was a higher proportion of mutation-positive women than men (17.6 per cent, compared to 6.3 per cent, p < 0.001), and a lower proportion with squamous cell carcinoma than for other histopathological subtypes (3.0 per cent, compared to 12.9 per cent, p < 0.001). Of a total of 80 cytological tests, nine (11.3 per cent) were positive. Interpretation. In light of the relatively high mutation frequency and a considerable number of positives in the group with squamous cell carcinoma, we recommend to continue the practice of mutation-testing all patients with non-small-cell lung cancer.