Actively Recruiting

Phase Not Applicable
Age: 70Years +
All Genders
NCT06923618

Cancer of the Lung And SeneScencE - Prospective Cohort 1

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-12-15

385

Participants Needed

1

Research Sites

364 weeks

Total Duration

On this page

Sponsors

A

Assistance Publique - Hôpitaux de Paris

Lead Sponsor

A

ARC Foundation and Inserm

Collaborating Sponsor

AI-Summary

What this Trial Is About

The main objective is to identify and assess the predictive value of ageing and senescence biomarkers (methylome, telomeres, inflammageing) and senescent cells in tissues to improve prognosis assessment older patients with locally or locally-advanced Non-Small Cell Lung Cancer (NSCLC).

CONDITIONS

Official Title

Cancer of the Lung And SeneScencE - Prospective Cohort 1

Who Can Participate

Age: 70Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 70 years and over
  • Local or locally advanced (Clinic stage I-IIIA) NSCLC (clinically or radiologically suspected or histologically proven)
  • Surgical curative intent
  • Signed informed consent (or signed by the curator or tutorship)
  • Affiliated to social security administrative care service
Not Eligible

You will not qualify if you...

  • Synchronous cancer diagnosed or strongly suspected within 6 months prior to inclusion, excluding basal cell cancer and prostate cancer with local treatment or active surveillance without systemic treatment
  • Subject deprived of liberty by judicial or administrative decision or under guardianship
  • Subject unable to understand the purpose and conditions of the study and unable to give consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Henri Mondor Hospital

Créteil, Île-de-France Region, France, 94000

Actively Recruiting

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Research Team

F

Florence CANOUÏ-POITRINE, PhD

CONTACT

A

Adèle BELLINO, Project advisor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

0

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