Patients treated at the Hôpital Nord de Marseille for at least one smoking-related pathology (atheroma, chronic bronchitis, non-progressive cancer \> 5 years) or with eligibility criteria for lung cancer screening (inclusion criteria in the NLST or NELSON studies or American recommendations) Interventional study with minimal risks and constraints, with evaluation of lung cancer prevalence; immunological, blood inflammatory and microbiota profile Determine the maximum clinical, radiological, and biological phenotyping completeness rate following the implementation of a new lung cancer screening care pathway with multidimensional clinical, radiological, and biological phenotyping capabilities
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
160
within 3 months after the V0 visit
within 3 months after the V0 visit
within 3 months after the V0 visit
Assistance Publique Hopitaux de Marseille
Marseille, France
number of complete phenotyping clinical, clinical
Time frame: 18 months
number of complete phenotyping radiological
Time frame: 18 months
number of complete phenotyping biological samples
Time frame: 18 months
Number of lung cancers diagnosed / Number of patients included
Time frame: 18 MONTHS
Number of stage ≤ IIB lung cancers / number of lung cancers diagnosed
Time frame: 18 MONTHS
Number of patients in partial smoking cessation / number of active smoking patients included
Time frame: 18 MONTHS
Satisfaction assessment
by scale SF-12
Time frame: 2 times (inclusion, 8 months)
Assessment of ANXIETY
by scale STAI-YA
Time frame: 2 times (inclusion, 8 months)
Number of initial positive scans / number of initial scans
Time frame: 18 months
Number of invasive procedures resulting in a diagnosis of a benign lesion / number of invasive procedures
Time frame: 18 months
Number of cardiovascular events / number of patients included
Time frame: 18 months
Number of oncological events (other than lung cancer) / number of patients included
Time frame: 18 months
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