Trials / Recruiting
RecruitingNCT05463796
InAdvance: Surveillance, Prevention, and Interception in a Population at Risk for Cancer
InAdvance: Surveillance, Prevention, and Interception in a Population at Risk For Cancer
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 5,000 (estimated)
- Sponsor
- Dana-Farber Cancer Institute · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Accepted
Summary
This research study is creating a way to collect and store specimens and information from participants who may be at an increased risk of developing cancer, or has been diagnosed with an early phase of a cancer or a family member who has a family member with a precursor condition for cancer. * The objective of this study is to identify exposures as well as clinical, molecular, and pathological changes that can be used to predict early development of cancer, malignant transformation, and risks of progression to symptomatic cancer that can ultimately be fatal. * The ultimate goal is to identify novel markers of early detection and risk stratification to drive potential therapeutic approaches to intercept progression to cancer.
Detailed description
The objective of this protocol is to obtain clinical information and facilitate the collection and distribution of specimens obtained during the course of clinical care or research participation. * Blood, buccal swabs, urine or tissue or other body fluids (including stool) may be specifically acquired for research in order to perform molecular and other types of analyses for research purposes. * These materials will be collected from all eligible participants who have a precursor lesion or an increased risk of cancer It is expected that about 5,000 people will take part in this research study.
Conditions
- Cancer Risk
- Cancer Predisposition Syndrome
- Hereditary Cancer Prediction
- Childhood Cancer Survivors
- Adult Cancer Survivors
- IARC Carcinogens
- Smoking History
- Lung Cancer
- Ductal/Lobular Carcinoma
- Barrett Esophagus
- Pancreatic Precursor Lesions
- Colonic Dysplasia/Adenomata
- Non-Alcoholic Fatty Liver Disease
- Non Alcoholic Steatohepatitis
- Cirrhosis
- High Grade Prostatic Epithelial Neoplasia
- High-grade Bladder Urothelial Dysplasia/Carcinoma in Situ
- Adenomatous Hyperplasia
- High-risk Oral Precancerous Diseases
- Melanocytic Lesion, Adult
- Hematologic Malignancy
- Lung; Node
- Serous Tubal Intraepithelial Carcinoma
- Endometrial Intraepithelial Neoplasia
- Cervical and Endocervical Carcinoma in Situ
- Vulvar Intraepithelial Neoplasia
- Nephrogenic Rests
- Benign Bone Lesions With Risk of Malignant Degeneration
- Giant Cell Tumor
- Osteochondroma
- Spitz Nevus
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Samples | Tissue samples will be collected during a routine visit. Participants will be asked to donate any of the following tissue types: Blood, Buccal swab (saliva) or mouthwash, Urine, Stool, Biopsy or surgical tissue (i.e., bone marrow),Bodily fluids, Other tissues |
Timeline
- Start date
- 2023-04-25
- Primary completion
- 2027-03-25
- Completion
- 2032-03-25
- First posted
- 2022-07-19
- Last updated
- 2025-08-07
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT05463796. Inclusion in this directory is not an endorsement.