Status:

NOT_YET_RECRUITING

Tumor Associated Neutrophils as a Biomarker of Chemo-immunotherapy Response in Locally Advanced Non-small Cell Lung Cancer : a Model Based on Neoadjuvant Strategy

Lead Sponsor:

University Hospital, Montpellier

Conditions:

Non-Small Cell Lung Cancer

Eligibility:

All Genders

18+ years

Brief Summary

evaluate the predictive value of circulating neutrophil DNA methylation profiles, identified from the ALCINA 2 cohort, on pre-treatment blood samples (T0), for the histological response to neoadjuvant...

Eligibility Criteria

Inclusion

  • Age ≥ 18 years.
  • Resectable non-small cell lung cancer (NSCLC), stage IIA to IIIB.
  • Lymph node status obtained by Positron Emission Tomoscintigraphy (PET)-scanner, confirmation of lymph node status by optional histological sampling (mediastinoscopy, thoracoscopy, echo-endoscopy).
  • No secondary lesions in the cerebrum or extra-cerebrum confirmed on brain MRI, PET scanner +/- injected cerebro-thoraco-abdomino-pelvic scanner.
  • Neoadjuvant immunochemotherapy strategy validated by a multidisciplinary consultation meeting (RCP) prior to the start of treatment.
  • Lung function compatible with thoracic surgery, patient meets surgical and anesthetic criteria for operability
  • Measurable disease according to RECIST criteria version 1.1

Exclusion

  • Previous systemic treatment for the same CBNPC.
  • Diagnosis of another solid tumor within the last 3 years, ‡ excluding non melanoma cutaneous and cervical carcinomas .
  • Contraindication to immunotherapy.
  • Non-objection to participate in research not collected.
  • Patients unable to read and/or write.
  • Inability to monitor patient during study period
  • Persons unable to express their consent.
  • Not affiliated to a social security scheme.
  • Persons under court protection.
  • Persons participating in another research study with an ongoing exclusion period.
  • Pregnant women

Key Trial Info

Start Date :

July 1 2025

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

December 30 2028

Estimated Enrollment :

72 Patients enrolled

Trial Details

Trial ID

NCT06974097

Start Date

July 1 2025

End Date

December 30 2028

Last Update

July 8 2025

Active Locations (1)

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CHU de Montpellier - Hôpital Arnaud de Villeneuve

Montpellier, Cedex 5, France, 34295