Diagnostic Outcomes among Patients with Positive Multi-Cancer Early Detection Test Results.
Elizabeth K O'Donnell, Tia L Kauffman, Sydney Asnis...
https://pubmed.ncbi.nlm.nih.gov/41721625/Actively Recruiting
Led by Dana-Farber Cancer Institute · Updated on 2025-08-07
5000
Participants Needed
1
Research Sites
261 weeks
Total Duration
Researchers are conducting a study to gather and store samples and information from individuals who might be at higher risk of developing cancer or have early-stage cancer or precursor conditions, as well as their family members. The study aims to identify exposures and clinical, molecular, and pathological changes that help predict early cancer development, progression, and malignant transformation. The ultimate goal is to find new markers for early detection and risk assessment that could guide future treatments to prevent cancer progression. Participants will provide tissue samples during routine visits, including blood, saliva or mouthwash, urine, stool, biopsy or surgical tissue such as bone marrow, bodily fluids, or other tissues. Participants will also complete a survey about their demographics, medical history, and family history. Family members of participants may also provide blood or saliva samples through various collection methods, including at consent, by mail, or at a separate appointment. During the study, participants will have clinical information and specimens collected for research analysis. Researchers will monitor exposures and changes over five years to understand cancer risk and progression. About 5,000 people are expected to participate. The study includes data collection from questionnaires, tissue sampling, and molecular analysis to identify markers that predict cancer development and progression. Participants health and safety are monitored throughout the study period, which can last several years.
CONDITIONS
InAdvance: Surveillance, Prevention, and Interception in a Population at Risk for Cancer
J
Jenna Beckwith, MPH
T
Tia Kauffman, MPH
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Dana-Farber Cancer Institute
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 5 years
Participants are observed and clinical information is collected during routine healthcare visits. Tissue samples such as blood, buccal swabs, urine, stool, biopsy or surgical tissue, and bodily fluids are collected for research purposes.
Visits occur during routine healthcare appointments; timing may vary
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
4
Have more questions? Get in touch with our team for quick support
Elizabeth K O'Donnell, Tia L Kauffman, Sydney Asnis...
https://pubmed.ncbi.nlm.nih.gov/41721625/Tia L Kauffman, Elizabeth K O'Donnell, Catherine R Marinac...
https://pubmed.ncbi.nlm.nih.gov/42059770/Dana-Farber Cancer Institute
Lead Sponsor