Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT06974097

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

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)

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHU de Montpellier - Hôpital Arnaud de Villeneuve

Montpellier, Cedex 5, 34295, France

Location contact

Camille TRAVERT

CONTACT

[email protected]

033467336135

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Blood sampling

Other

blood sampling

Primary outcomes

  1. Area under the ROC curve (AUC) of neutrophil DNA methylation profiles for predicting histologic response

    Time frame: 6 Months after inclusion

Study contacts

Contact information is provided by the study sponsor or research team.

Anne CADENE

CONTACT

[email protected]

0 33 4 67 33 08 14

Camille TRAVERT, Principal Investigator

CONTACT

[email protected]

033 4 67 33 61 35

Sponsors and collaborators

Lead sponsor

University Hospital, Montpellier

Other

Registry information

Acronym: NEO-TAN

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
May 15, 2025
Registry last updated
Jul 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.