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

University Hospital Center (CHU) logo

University Hospital Center (CHU)

Status

Not yet enrolling

Conditions

Non-Small Cell Lung Cancer

Treatments

Other: blood sampling

Study type

Observational

Funder types

Other

Identifiers

NCT06974097
RECHMPL24_0275

Details and patient eligibility

About

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 chemo-immunotherapy in patients with resectable non-small cell lung cancer (NSCLC)

Enrollment

72 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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 criteria

  • 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

Trial contacts and locations

1

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Central trial contact

Anne CADENE; Camille TRAVERT, Principal Investigator

Data sourced from clinicaltrials.gov

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