Actively Recruiting
Integrating Artificial Intelligence Into Lung Cancer Screening.
Led by Centre Hospitalier Universitaire de Nice · Updated on 2024-04-12
2722
Participants Needed
1
Research Sites
338 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Lung cancer (LC) screening using low-dose chest CT (LDCT) has already proven its efficacy. The mortality reduction associated with LC screening is around 20%, much higher than the reduction in mortality associated with screening for breast, colon or prostate cancers. Implementing lung cancer screening on a large scale faces two main obstacles: 1. The lack of thoracic radiologists and LDCT necessary for the eligible population (between 1.6 and 2.2 million people in France); 2. The high frequency of false positive screenings: in the NLST trial, more than 20% of the subjects screened were found to have at least one nodule of an indeterminate lung nodule (ILN) whereas less than 3% of ILNs are actually LC. The gold standard for determining on the benign or malignant nature of a nodule is definitive histology. Otherwise, the evolution of the nodule on serial thoracic imaging is a good alternative. The period of indeterminacy of a nodule can be as long as 24 months in many cases, which can be a source of prolonged and sometimes unjustified anxiety for screening candidates. The purpose of this randomized controlled study that focuses on LC screening in patients aged 50 to 80 years, who smoked more than 20 packs/ year or stopped smoking less than 15 years ago. Its objective is to determine whether assisting multidisciplinary team (MDT) meetings with an AI-based analysis of screening LDCT accelerates the definitive classification of nodules into malignant or benign.
CONDITIONS
Official Title
Integrating Artificial Intelligence Into Lung Cancer Screening.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 50 and 80 years old
- Active smoker or ex-smoker who quit smoking less than 15 years ago
- Smoking history of at least 20 pack-years
- Signed informed consent
- Affiliated to French social security
You will not qualify if you...
- Clinical signs suggestive of cancer
- Chest scan within the past year for another cause
- Radiological abnormalities requiring follow-up or additional investigations
- Health problems significantly limiting life expectancy
- Health problems limiting ability or willingness to undergo lung surgery
- Active cancer except basal cell carcinoma of the skin
- Vulnerable adults under guardianship or curatorship
- Medical or psychiatric problems limiting study adherence or increasing risk
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHU de Nice - Hôpital de Pasteur
Nice, Alpes-maritimes, France, 06001
Actively Recruiting
Research Team
M
Marquette Charles-Hugo, PhD
CONTACT
B
Boutros Jacques
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
DIAGNOSTIC
Number of Arms
2
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