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Clinical Trials/NCT03951233
NCT03951233
Completed
Not Applicable

Genotyping K-RAS and EGFR in Greek Non-small-cell Lung Cancer Patients: Incidence, Significance and Treatment Implications

Hellenic Cooperative Oncology Group1 site in 1 country424 target enrollmentMarch 2000

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non Small Cell Lung Cancer
Sponsor
Hellenic Cooperative Oncology Group
Enrollment
424
Locations
1
Primary Endpoint
Progression free survival
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Retrospective analysis where patients with histologically confirmed Non-small cell lung cancer (NSCLC) were centrally evaluated for the presence of KRAS and EGFR mutations.

Detailed Description

A retrospective analysis, performed by the Hellenic Co-operative Oncology Group (HeCOG), in samples from patients with histologically confirmed NSCLC, who had been treated within HeCOG-affiliated centres from March 2000 through December 2012, were centrally evaluated for the presence of KRAS and EGFR mutations. All patients had available clinicopathological data at diagnosis. Formalin-fixed, paraffin-embedded tissue blocks were retrospectively retrieved from the HeCOG tumor repository. Cytologic material was prospectively submitted for genotyping in more recent years (2010-2012).

Registry
clinicaltrials.gov
Start Date
March 2000
End Date
December 2014
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Hellenic Cooperative Oncology Group
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with histologically confirmed NSCLC
  • Signed and dated written informed consent
  • Age 18 years
  • Available cytological material

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Progression free survival

Time Frame: from the date of treatment start until verified disease progression, death from any cause or date of last contact whichever occurred first, up to 9 months

Overall survival

Time Frame: from the date of treatment start until verified disease progression, death from any cause or date of last contact whichever occurred first, up to 36 months

Study Sites (1)

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