Prevalence and clinical association of gene mutations through Multiplex Mutation Testing in patients with NSCLC: Results from the ETOP Lungscape Project.

2.50
Hdl Handle:
http://hdl.handle.net/10541/620771
Title:
Prevalence and clinical association of gene mutations through Multiplex Mutation Testing in patients with NSCLC: Results from the ETOP Lungscape Project.
Authors:
Kerr, K; Dafni, U; Schulze, K; Thunnissen, E; Bubendorf, L; Hager, H; Finn, S; Biernat, W; Vliegen, L; Losa, J; Marchetti, A; Cheney, R; Warth, A; Speel, E; Blackhall, Fiona H ( 0000-0001-8716-3395 ) ; Monkhorst, K; Jantus Lewintre, E; Tischler, V; Clark, C; Bertran-Alamillo, J; Meldgaard, P; Gately, K; Wrona, A; Vandenberghe, P; Felip, E; De Luca, G; Savic, S; Muley, T; Smit, E; Dingemans, A; Priest, L; Baas, P; Camps, C; Weder, W; Polydoropoulou, V; Geiger, T; Kammler, R; Sumiyoshi, T; Molina, M; Shames, D; Stahel, R; Peters, S
Abstract:
Reported prevalence of driver gene mutations in non-small cell lung cancer (NSCLC) is highly variable and clinical correlations are emerging. Using NSCLC biomaterial and clinical data from the ETOP Lungscape iBiobank, we explore the epidemiology of mutations and association to clinicopathological features and patient outcome (relapse-free survival, time-to-relapse, overall survival).
Affiliation:
Department of Pathology, Aberdeen Royal Infirmary, Aberdeen
Citation:
Prevalence and clinical association of gene mutations through Multiplex Mutation Testing in patients with NSCLC: Results from the ETOP Lungscape Project. 2017 Ann Oncol
Journal:
Annals of Oncology
Issue Date:
23-Nov-2017
URI:
http://hdl.handle.net/10541/620771
DOI:
10.1093/annonc/mdx629
PubMed ID:
29186353
Type:
Article
Language:
en
ISSN:
1569-8041
Appears in Collections:
All Christie Publications

Full metadata record

DC FieldValue Language
dc.contributor.authorKerr, Ken
dc.contributor.authorDafni, Uen
dc.contributor.authorSchulze, Ken
dc.contributor.authorThunnissen, Een
dc.contributor.authorBubendorf, Len
dc.contributor.authorHager, Hen
dc.contributor.authorFinn, Sen
dc.contributor.authorBiernat, Wen
dc.contributor.authorVliegen, Len
dc.contributor.authorLosa, Jen
dc.contributor.authorMarchetti, Aen
dc.contributor.authorCheney, Ren
dc.contributor.authorWarth, Aen
dc.contributor.authorSpeel, Een
dc.contributor.authorBlackhall, Fiona Hen
dc.contributor.authorMonkhorst, Ken
dc.contributor.authorJantus Lewintre, Een
dc.contributor.authorTischler, Ven
dc.contributor.authorClark, Cen
dc.contributor.authorBertran-Alamillo, Jen
dc.contributor.authorMeldgaard, Pen
dc.contributor.authorGately, Ken
dc.contributor.authorWrona, Aen
dc.contributor.authorVandenberghe, Pen
dc.contributor.authorFelip, Een
dc.contributor.authorDe Luca, Gen
dc.contributor.authorSavic, Sen
dc.contributor.authorMuley, Ten
dc.contributor.authorSmit, Een
dc.contributor.authorDingemans, Aen
dc.contributor.authorPriest, Len
dc.contributor.authorBaas, Pen
dc.contributor.authorCamps, Cen
dc.contributor.authorWeder, Wen
dc.contributor.authorPolydoropoulou, Ven
dc.contributor.authorGeiger, Ten
dc.contributor.authorKammler, Ren
dc.contributor.authorSumiyoshi, Ten
dc.contributor.authorMolina, Men
dc.contributor.authorShames, Den
dc.contributor.authorStahel, Ren
dc.contributor.authorPeters, Sen
dc.date.accessioned2018-01-12T09:19:08Z-
dc.date.available2018-01-12T09:19:08Z-
dc.date.issued2017-11-23-
dc.identifier.citationPrevalence and clinical association of gene mutations through Multiplex Mutation Testing in patients with NSCLC: Results from the ETOP Lungscape Project. 2017 Ann Oncolen
dc.identifier.issn1569-8041-
dc.identifier.pmid29186353-
dc.identifier.doi10.1093/annonc/mdx629-
dc.identifier.urihttp://hdl.handle.net/10541/620771-
dc.description.abstractReported prevalence of driver gene mutations in non-small cell lung cancer (NSCLC) is highly variable and clinical correlations are emerging. Using NSCLC biomaterial and clinical data from the ETOP Lungscape iBiobank, we explore the epidemiology of mutations and association to clinicopathological features and patient outcome (relapse-free survival, time-to-relapse, overall survival).en
dc.language.isoenen
dc.rightsArchived with thanks to Annals of oncology : official journal of the European Society for Medical Oncologyen
dc.titlePrevalence and clinical association of gene mutations through Multiplex Mutation Testing in patients with NSCLC: Results from the ETOP Lungscape Project.en
dc.typeArticleen
dc.contributor.departmentDepartment of Pathology, Aberdeen Royal Infirmary, Aberdeenen
dc.identifier.journalAnnals of Oncologyen

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