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

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    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
    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
    Show allShow less
    Affiliation
    Department of Pathology, Aberdeen Royal Infirmary, Aberdeen
    Issue Date
    2017-11-23
    
    Metadata
    Show full item record
    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).
    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
    URI
    http://hdl.handle.net/10541/620771
    DOI
    10.1093/annonc/mdx629
    PubMed ID
    29186353
    Type
    Article
    Language
    en
    ISSN
    1569-8041
    ae974a485f413a2113503eed53cd6c53
    10.1093/annonc/mdx629
    Scopus Count
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