| Literature DB >> 24589437 |
Vincent Fallet1, Jacques Cadranel1, Hélène Doubre2, Cécile Toper3, Isabelle Monnet4, Thierry Chinet5, Gérard Oliviero6, Guillaume Foulon7, Hubert De Cremoux8, Thibault Vieira9, Martine Antoine10, Marie Wislez11.
Abstract
The aim of this study was to analyse the clinico-pathological characteristics and outcomes of a cohort of French patients who were prospectively screened for Anaplastic Lymphoma Kinase (ALK) rearrangement. One hundred and sixteen consecutive patients screened for ALK rearrangement to be recruited into a crizotinib registration trial were included from eight French centres. ALK rearrangement was detected by fluorescence in situ hybridization. Seventeen patients (14.6%) were positive for ALK. ALK+ patients were younger (p = 0.049) and more likely to be males (p=0.032), non- or light-smokers (p = 0.048) and without underlying respiratory disease (p=0.025) compared to ALK- patients. Thyroid-transcription factor-1 expression was present in all ALK+ tumours. ALK+ tumours tended to have lymph node and brain metastases. In multivariate analyses, gender, smoking history and N stage were independently associated with ALK status. Median overall survival (OS) was not reached for ALK+ patients and was significantly longer than for ALK- patients (hazard ratio for death for ALK- patients 2.98; 95% CI [1.29-6.90], p=0.01). French ALK+ patients present a specific phenotype. ALK rearrangement should be determined to improve OS with an effective targeted therapy.Entities:
Keywords: Adenocarcinoma; Crizotinib; EML4-ALK fusion protein; Lung neoplasms; Non-small-cell lung; Survival analysis
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Year: 2014 PMID: 24589437 DOI: 10.1016/j.ejca.2014.02.001
Source DB: PubMed Journal: Eur J Cancer ISSN: 0959-8049 Impact factor: 9.162