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Not yet recruitingNCT07085429BCBPoumonUpdated Jul 25, 2025

Development of Clinical and Biological Database on Bronchial Cancer

An interventional study of Blood and tissue sampling in Lung Cancer and Bronchial Cancer, sponsored by Institut du Cancer de Montpellier - Val d'Aurelle. Not yet recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-07-25.

Sponsored by Institut du Cancer de Montpellier - Val d'Aurelle · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
750
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

A Clinical and Biological Database will provide to the scientific community a collection of blood and tissues with clinical data to improve knowledge about cancer and help to develope new cancer treatments. This database is specific to bronchial cancer.

Read the detailed description

Lung cancer is the leading cause of cancer-related mortality and the third most commonly diagnosed cancer. In France in 2018, it accounted for 46,363 new cases and 33,117 deaths. The overall 5-year survival rate across all stages and sexes is 20%.

Diagnosis is most often made at the metastatic stage, which significantly worsens the prognosis. Since 2020, the standard treatment for such cases has been the administration of intravenous chemo-immunotherapy, in the absence of a molecular alteration that allows for access to an oral targeted therapy. Immunotherapy and targeted therapies have considerably improved the prognosis for some patients, but the vast majority experience therapeutic resistance, either early or delayed.

The prognostic and predictive mechanisms of treatment response are poorly understood and vary greatly between histological and molecular subtypes. It is therefore crucial to gain a better understanding of these mechanisms in order to ultimately identify new therapeutic avenues to improve patient outcomes.

The first step in this process is to establish a tissue and blood biobank from patients with bronchial carcinoma (both small-cell and non-small-cell) treated at our center.

The Clinical Biological DataBase (BCB) is a tool:

  • for research in analytical and public health epidemiology, biological research and for the development of data useful for clinical research and therapeutic trials;
  • to help scientists understand and explain phenomena ranging from the interaction of molecules to the whole metabolism of the organism in normal and pathological situations;
  • to identify potential strategies for prevention, diagnosis, management and analysis of cancer subtypes.
02

Conditions studied

  • Lung Cancer
  • Bronchial Cancer
03

In context

Lung Neoplasms

7,243 studies on the registry are indexed under Lung Neoplasms; 1,557 are open to participants now.

This study's planned enrollment of 750 is above the median of 60 across 5,295 interventional studies indexed under Lung Neoplasms.

Browse Lung Neoplasms studies →

Lead sponsor

Institut du Cancer de Montpellier - Val d'Aurelle is the lead sponsor of 138 studies on the registry; 47 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Male or female patient aged over 18 years,
  • Histologically or cytologically confirmed bronchial cancer,
  • Treatment-naïve patient for the current cancer,
  • Patient who has provided informed, written, and explicit consent,
  • Patient affiliated with the French national health insurance system.

Exclusion criteria

Exclusion Criteria:

  • Patient with a WHO performance status ≥ 3,
  • Pregnant and/or breastfeeding woman,
  • Patient with a history of other cancers within the 5 years preceding inclusion,
  • Patient for whom regular follow-up is considered impossible due to psychological, familial, social, or geographic reasons,
  • Patient under legal protection (guardianship, curatorship, or judicial protection).
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
750 participants (estimated)

Study arms

  • Experimental
    Bronchial cancer

    Additionnal samples from routine care of different natures (blood, tumor tissue ans healthy tissue) and standardized clinical data will be entered into a database.

    Biological: Blood and tissue sampling

Interventions

  • BiologicalBlood and tissue sampling

    Tissue samples (tumor tissue and healthy tissue) frozen and secured in paraffin collected during surgery. During the blood samples taken for diagnosis and / or treatment when possible. Additional samples for research purposes will be carried out, these blood samples will be collected: * before any therapeutic intervention (T1) for a total volume of 36mL, * prior to surgery (T-Surg) for a total volume of 24mL, * at each progression (T2a, b, c…) for a total volume of 24mL, * at the end of follow-up (T3) for a total volume of 24mL.

06

What researchers measure

Primary outcomes

  1. Proportion of patients who consent to participate in the study

    the proportion of patients who consent to participate in the study among the screened patients

    Time frame: through study completion : an average of 1 year

07

Study locations

1 site
  • Centre Regional de Lutte Contre le Cancer - Centre Val d'Aurelle
    Montpellier, France 34298, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 25, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07085429
Lead sponsor
Institut du Cancer de Montpellier - Val d'Aurelle
Responsible party
Sponsor
First posted
Jul 25, 2025
Start date
Sep 2025 (estimated)
Primary completion
Sep 2030 (estimated)
Completion
Sep 2040 (estimated)
Last update
Jul 25, 2025

Study contacts

Emmanuelle TEXIER
Contact
emmanuelle.texier@icm.unicancer.fr
467613102 ext. +33

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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