Actively Recruiting
Nodule Immunophenotyping Biomarker for Lung Cancer Early Diagnosis Study
Led by Royal Marsden NHS Foundation Trust · Updated on 2023-06-15
500
Participants Needed
9
Research Sites
260 weeks
Total Duration
On this page
Sponsors
R
Royal Marsden NHS Foundation Trust
Lead Sponsor
R
Royal Brompton & Harefield NHS Foundation Trust
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the use of artificial intelligence and machine learning-based radiomics to distinguish between benign and malignant lung nodules in patients who have previously been treated for cancer. The study focuses on incidental lung nodules detected during routine care, aiming to improve early diagnosis of lung cancer and differentiate between metastatic recurrence and new primary lung cancer. This observational study seeks to enhance current risk models by integrating imaging and blood biomarker data. Participants under active investigation or surveillance for incidental lung nodules will be included. The study involves collecting blood samples for high-dimensional immune phenotyping and analyzing imaging data to develop biomarkers that predict cancer risk. The study also explores combining blood and imaging biomarkers to improve malignancy prediction. This research builds on previous lung screening programs and aims to reduce unnecessary imaging and invasive procedures. During the study, participants will undergo regular CT scans and blood sampling to monitor lung nodules and immune profiles over time. Researchers will assess immune phenotypes and imaging characteristics to identify markers associated with cancer development or relapse. The primary and secondary outcomes will be evaluated over a 10-year period, with long-term follow-up to track changes in risk scores after tumor treatment or regression. This approach aims to support more personalized surveillance strategies for lung nodules.
CONDITIONS
Brief Title
Nodule IMmunophenotyping Biomarker for Lung Cancer Early Diagnosis Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients under active investigation or surveillance for incidental lung nodules
- Age over 18 years
You will not qualify if you...
- Active or previous diagnosis of malignancy within 5 years preceding baseline scan
- Inability to give informed consent
- Active infection including tuberculosis or fungal infection
- Clinician-suspected or confirmed active or recent COVID-19 infection within 4 weeks before CT scan or blood sampling
Research Team
S
Sejal Jain
L
Laura Boddy
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