Prospective Multicenter Cohort Study to Validate Four Groups of Biomarkers for Assessing Lung Cancer Risk Among Patients With Atheromatous Cardiovascular Disease in a Screening Pathway

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age45-80
SponsorAssistance Publique Hopitaux De Marseille

About this trial

Interventional study with minimal risks and constraints, with evaluation of the incidence of lung cancers by low-dose thoracic CT scan without injection of contrast medium, of the immunological, inflammatory and metabolic blood profile and of the microbiota; systematic proposal of smoking cessation for active smokers or assistance in maintaining cessation.

Eligibility criteria

Qualifiers

1- All PREVALUNG or PREVALUNG ETOILE participants

2- Active or former smokers who have smoked daily for at least 10 years and have either atheromatous disease (coronary, lower limb, supra-aortic trunk, aortic, visceral or upper limb arteries) or a moderate or high coronary calcium score*, **.

Age 45- 75 years and

Medical follow-up for smoking-related atheromatous pathology and

Disqualifiers

cancer history < 5 years (except carcinoma in situ of the uterine cervix, basal cell carcinoma of the skin, non-invasive urothelial carcinoma treated for curative purposes without CT lung surveillance, prostate cancer with unmeasurable PSA)

symptoms of lung cancer (involuntary weight loss > 7 kg in 1 year, hemoptysis)

known history of pulmonary nodule requiring specialized follow-up

history of pulmonary fibrosis or pulmonary hypertension

Trial design

Treatments tested in this trial

  • blood sampling
  • stool collection
  • low dose CT scan

Treatment groups

750 Participants
are divided into 1 treatment group