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Cohort of Non-small Cell Lung Cancer With Mutation of the Nord Pas de Calais (CB(NPC)²)

Cohort of Non-small Cell Lung Cancer With Mutation of the Nord Pas de Calais

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02448758
Acronym
CB(NPC)²
Enrollment
518
Registered
2015-05-19
Start date
2013-11-01
Completion date
2017-09-01
Last updated
2026-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-Small Cell Lung Cancer

Keywords

mutation

Brief 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.

Detailed 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.

Interventions

None listed

Sponsors

Centre Oscar Lambret
Lead SponsorOTHER
University Hospital, Lille
CollaboratorOTHER
Centre de Biologie Pathologie : Plateforme de Biologie Moléculaire de Lille
CollaboratorUNKNOWN

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Correlation between clinical factors and mutation statusat baselineThe clinical factors are age, smoking status, occupational and environmental exposure, personal and family background, TNM stage, performance status

Secondary

MeasureTime frame
Progression-free survival3 years
Overall survival3 years
Number of patients included in a clinical trial dedicated to a certain type of non-small cell lung cancer with mutation3 years
Number of cases per mutation type3 years

Countries

France

Contacts

STUDY_DIRECTORAlexis CORTOT, MD, PhD

CHRU of Lille

STUDY_DIRECTOREric Dansin, MD

Centre Oscar Lambret

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 14, 2026