This is a non-interventional diagnostic, international, multicenter and non-comparative study of EGFR mutation status in aNSCLC patients (locally advanced and/or metastatic disease) with adenocarcinoma and non-adenocarcinoma histologies. This study will be conducted in Japan and Europe and will assess the concordance of EGFR mutation status derived from tumour samples and blood based circulating free DNA. The data generated will inform the use of less-invasive sample types in diagnostic practice. The study also aims to assess the current status of EGFR mutation testing across Japan and Europe and gaps in currently available data including EGFR mutation frequency in particular populations and demographic subgroups, EGFR mutation frequency in histological subtypes of NSCLC, EGFR mutation test process and methodology, utility of multiple sample types in the assessment of EGFR mutation status, and impact of EGFR mutation status on therapy choice. The data may be used to drive improvements to the EGFR mutation testing process, ensuring that patients have access to testing and are treated appropriately on the basis of the molecular features of their disease.
A diagnostic Study of European and Japanese advanced NSCLC patients to evaluate suitable sample types for EGFR testing,
Study Type
OBSERVATIONAL
Enrollment
1,311
Research Site
Compiègne, France
Research Site
Gap, France
Research Site
Le Mans, France
Research Site
Longjumeau, France
Research Site
Meaux, France
Research Site
Saint-Brieuc, France
Determination of the level of concordance between EGFR mutation status obtained via tissue/cytology and blood (plasma) based testing.
Time frame: From randomization until study completion, assessed up to 17 months
Determination of the EGFR mutation frequency (including mutation subtypes) in patients with advanced NSCLC (aNSCLC) of adenocarcinoma and non-adenocarcinoma histologies.
Time frame: From randomization until study completion, assessed up to 17 months.
Describe the first line therapy choice following EGFR mutation testing.
Time frame: From randomization until study completion, assessed up to 17 months.
Describe the second line therapy choice following discontinuation of first line treatment for patients confirmed as EGFR mutation positive via tissue/cytology.
Time frame: From randomization until study completion, assessed up to 17 months.
Summary of EGFR mutation testing practices in terms of methods, sample types, success rate, mutation detection rate, testing turnaround time and reasons for not testing.
Time frame: From randomization until study completion, assessed up to 17 months.
Determination of the correlation between EGFR mutation status from tumour and demographic data and disease status.
Time frame: From randomization until study completion, assessed up to 17 months.
Determination of the correlation between EGFR mutation status derived from plasma (blood) and demographic data and disease status.
Time frame: From randomization until study completion, assessed up to 17 months.
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Research Site
Saint-Michel, France
Research Site
Saint-Quentin, France
Research Site
Villefranche-sur-Saône, France
Research Site
Buch, Germany
...and 47 more locations