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Clinical Trials/NCT01838577
NCT01838577
Unknown
Not Applicable

Genetics of EGFR Mutation Study (GEM): a Translational Study of the EORTC Lung Group.

European Organisation for Research and Treatment of Cancer - EORTC1 site in 1 country2,000 target enrollmentSeptember 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
EGFR Mutation Positive Non Small Cell Lung Cancer
Sponsor
European Organisation for Research and Treatment of Cancer - EORTC
Enrollment
2000
Locations
1
Primary Endpoint
For the second objective, the primary endpoint is Overall survival (OS)
Last Updated
5 years ago

Overview

Brief Summary

The investigators wish to document the distribution of EGFR somatic mutations, and assess the relationship between specific genotype, clinical demographic, therapy, and survival, in a large cohort of EGFR mutant NSCLC.

The investigators also wish to comprehensively investigate the relationship between germline DNA and risk of EGFR mutant NSCLC developing, through a GWAS (Genome-Wide Association Studies) and candidate gene approach, and explore the relationship between germline DNA and clinical outcome, in order to potentially identify germline genetic modifiers of EGFR TKI (Tyrosine Kinase Inhibitor) outcome.

Detailed Description

Objective 1: To identify germline allelic DNA variation associated with somatic EGFR mutation in NSCLC, Objective 2: Correlation between germline allelic variants and survival in EGFR somatic mutant NSCLC. Objective 3: Study germline allelic DNA variation associated with never /ex light smoking NSCLC. Objective 4: Catalogue distribution of somatic EGFR mutant genotypes in 1,000 EGFR mutant NSCLC cases and describe their relationship to clinical outcome.

Registry
clinicaltrials.gov
Start Date
September 2013
End Date
March 2022
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

For the second objective, the primary endpoint is Overall survival (OS)

Time Frame: 5 years from FPI

Study Sites (1)

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