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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02448758
Other study ID # CB(NPC)²-1209
Secondary ID
Status Recruiting
Phase N/A
First received March 6, 2014
Last updated May 15, 2015
Start date September 2011
Est. completion date September 2017

Study information

Verified date May 2015
Source Centre Oscar Lambret
Contact Alexis CORTOT, MD, PhD
Phone +33 3 20 44 56 12
Email alexis.cortot@chru-lille.fr
Is FDA regulated No
Health authority France: Comité consultatif sur le traitement de l'information en matière de recherche dans le domaine de la santéFrance: The Commission nationale de l’informatique et des libertés
Study type Observational

Clinical Trial Summary

The investigators propose to create a database at the regional level, the principle is to include all patients in whom a mutation was detected from a single platform (Lille). The creation of this regional cohort, smaller than the national cohort of Biomarkers France, will perform a more comprehensive collection of clinical data, and molecular monitoring data of patients included. To increase the completeness of the collection of information, it will not be based on voluntary prescribing clinician but will be largely carried out by CRA dedicated to this activity.


Description:

This is a prospective and retrospective study of a population of patients with mutated non-small cell lung cancer in the Nord Pas de Calais. Retrospective cohort will involve patients with main molecular abnormalities, identifiable from molecular biology platform CRRC, except EGFR and KRAS treated from September 2011 to February 2013.


Recruitment information / eligibility

Status Recruiting
Enrollment 785
Est. completion date September 2017
Est. primary completion date September 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Aged = 18 years old

- Patient with non-small cell lung cancer

- Detected in the Nord Pas de Calais

- Monitored in the Nord Pas de Calais

- Patient must have signed a non-opposition form to the use of medical data

Exclusion Criteria:

- No identified mutation

Study Design

Observational Model: Cohort


Locations

Country Name City State
France Centre Oscar Lambret Lille
France CHRU Lille

Sponsors (3)

Lead Sponsor Collaborator
Centre Oscar Lambret Centre de Biologie Pathologie : Plateforme de Biologie Moléculaire de Lille, University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation between clinical factors and mutation status The clinical factors are age, smoking status, occupational and environmental exposure, personal and family background, TNM stage, performance status at baseline No
Secondary Progression-free survival 3 years No
Secondary Overall survival 3 years No
Secondary Number of patients included in a clinical trial dedicated to a certain type of non-small cell lung cancer with mutation 3 years No
Secondary Number of cases per mutation type 3 years No
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