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Prognostic role of FGFR1 amplification in early-stage non-small cell lung cancer.

AbstractBACKGROUND:
Recently, fibroblast growth factor receptor 1 (FGFR1) was discovered in squamous cell carcinomas (SCC) of the lung with FGFR1 amplification described as a promising predictive marker for anti-FGFR inhibitor treatment. Only few data are available regarding prevalence, prognostic significance and clinico-pathological characteristics of FGFR1-amplified and early-stage non-small cell lung carcinomas (NSCLC). We therefore investigated the FGFR1 gene status in a large number of well-characterised early-stage NSCLC.
METHODS:
FGFR1 gene status was evaluated using a commercially available fluorescent in situ hybridisation (FISH) probe on a tissue microarray (TMA). This TMA harbours 329 resected, formalin-fixed and paraffin-embedded, nodal-negative NSCLC with a UICC stage I-II. The FISH results were correlated with clinico-pathological features and overall survival (OS).
RESULTS:
The prevalence of an FGFR1 amplification was 12.5% (41/329) and was significantly (P<0.0001) higher in squamous cell carcinoma (SCC) (20.7%) than in adenocarcinoma (2.2%) and large cell carcinoma (13%). Multivariate analysis revealed significantly (P=0.0367) worse 5-year OS in patients with an FGFR1-amplified NSCLC.
CONCLUSIONS:
FGFR1 amplification is common in early-stage SCC of the lung and is an independent and adverse prognostic marker. Its potential role as a predictive marker for targeted therapies or adjuvant treatment needs further investigation.
AuthorsN Cihoric, S Savic, S Schneider, I Ackermann, M Bichsel-Naef, R A Schmid, D Lardinois, M Gugger, L Bubendorf, I Zlobec, C Tapia
JournalBritish journal of cancer (Br J Cancer) Vol. 110 Issue 12 Pg. 2914-22 (Jun 10 2014) ISSN: 1532-1827 [Electronic] England
PMID24853178 (Publication Type: Journal Article)
Chemical References
  • FGFR1 protein, human
  • Receptor, Fibroblast Growth Factor, Type 1
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Carcinoma, Non-Small-Cell Lung (genetics, mortality)
  • Carcinoma, Squamous Cell (genetics, mortality)
  • Disease-Free Survival
  • Female
  • Gene Amplification
  • Humans
  • In Situ Hybridization, Fluorescence
  • Lung Neoplasms (genetics, mortality)
  • Male
  • Middle Aged
  • Neoplasm Recurrence, Local (genetics)
  • Receptor, Fibroblast Growth Factor, Type 1 (genetics)
  • Tissue Array Analysis

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