Actively Recruiting

All Genders
Healthy Volunteers
NCT05463796

InAdvance: Surveillance, Prevention, and Interception in a Population at Risk for Cancer

Led by Dana-Farber Cancer Institute · Updated on 2025-08-07

5000

Participants Needed

1

Research Sites

465 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

InAdvance: Surveillance, Prevention, and Interception in a Population at Risk for Cancer

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants with hereditary cancer risk including carriers of pathogenic germline variants or clinical cancer predisposition syndromes
  • Individuals with personal or family history suggesting elevated cancer risk
  • Childhood and adult cancer survivors with treatment exposures increasing cancer risk
  • Documented high exposure to group 1 IARC carcinogens
  • Individuals at risk for lung cancer by age over 50, smoking history over 15 pack years, or family history of lung cancer or COPD
  • Participants with alcoholic liver disease, non-alcoholic steatohepatitis, or cirrhosis
  • Participants with certain precursor lesions such as ductal/lobular carcinoma in situ, Barrett's esophagus, pancreatic precursor lesions, colonic dysplasia, high-grade prostatic neoplasia, and others
  • Family members or healthy individuals related to at-risk participants
Not Eligible

You will not qualify if you...

  • None; there are no exclusion criteria for this study

AI-Screening

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Trial Site Locations

Total: 1 location

1

Dana Farber Cancer Institute

Boston, Massachusetts, United States, 02115

Actively Recruiting

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Research Team

J

Jenna Beckwith, MPH

CONTACT

T

Tia Kauffman, MPH

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

4

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InAdvance: Surveillance, Prevention, and Interception in a Population at Risk for Cancer | DecenTrialz