RECRUITING

The Vanguard Study: Testing a New Way to Screen for Cancer

Description

The Vanguard Study is a feasibility study to explore several aspects of evaluating multi-cancer detection (MCD) tests in a future definitive randomized controlled trial. An MCD test measures markers in the blood in order to screen for multiple cancers simultaneously. There is a need to understand how MCDs may work as cancer screening tools. The goal of cancer screening is to reduce the burden of cancer by identifying cancers before they show symptoms or signs, when treatment is likely to be most effective. In this study, adults aged 45-75 without cancer will be randomly assigned to one of 3 groups: 2 separate MCD test groups or a control group. These two MCD tests will not be compared to each other but will be compared to cancers detected in the control group. This study will provide early information on how well MCD tests perform as cancer screening tools. It will also help researchers understand how patients and their doctors make decisions about their care when the MCD test result comes back as normal (negative) or abnormal (positive).

Study Overview

Study Details

Study overview

The Vanguard Study is a feasibility study to explore several aspects of evaluating multi-cancer detection (MCD) tests in a future definitive randomized controlled trial. An MCD test measures markers in the blood in order to screen for multiple cancers simultaneously. There is a need to understand how MCDs may work as cancer screening tools. The goal of cancer screening is to reduce the burden of cancer by identifying cancers before they show symptoms or signs, when treatment is likely to be most effective. In this study, adults aged 45-75 without cancer will be randomly assigned to one of 3 groups: 2 separate MCD test groups or a control group. These two MCD tests will not be compared to each other but will be compared to cancers detected in the control group. This study will provide early information on how well MCD tests perform as cancer screening tools. It will also help researchers understand how patients and their doctors make decisions about their care when the MCD test result comes back as normal (negative) or abnormal (positive).

The Vanguard Study: Testing a New Way to Screen for Cancer

The Vanguard Study: Testing a New Way to Screen for Cancer

Condition
Bladder Carcinoma
Intervention / Treatment

-

Contacts and Locations

Oklahoma City

University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States, 73104

Charlottesville

Sentara Martha Jefferson Hospital, Charlottesville, Virginia, United States, 22901

Fairfax

Inova Schar Cancer Institute, Fairfax, Virginia, United States, 22031

Norfolk

Sentara Norfolk General Hospital, Norfolk, Virginia, United States, 23507

Richmond

VCU Massey Cancer Center at Stony Point, Richmond, Virginia, United States, 23235

Richmond

Virginia Commonwealth University/Massey Cancer Center, Richmond, Virginia, United States, 23298

South Hill

VCU Community Memorial Health Center, South Hill, Virginia, United States, 23970

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Ages 45-75 years old
  • * Agree to provide blood samples for possible MCD testing at enrollment and at 1 year following enrollment
  • * Agree to allow collection of information from their medical records for study-related purposes
  • * Understand and be able to complete informed consent and participant questionnaires in English, Spanish, or Arabic
  • * Note: Eligibility for Spanish and Arabic languages are at the Hub's discretion
  • * Solid malignant tumor or blood cancer diagnosis, with or without treatment, within the last 5 years
  • * Note: Persons with a history of in situ cancers (e.g., ductal carcinoma in situ of the breast, cervical cancer in situ, atypical melanocytic hyperplasia or melanoma in situ) or nonmelanoma skin cancer are eligible
  • * Ongoing cancer diagnostic work-up
  • * Ongoing participation in another study of an investigational cancer screening test or technology
  • * Currently breastfeeding or pregnant, or planning to become pregnant in the next year

Ages Eligible for Study

45 Years to 75 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

National Cancer Institute (NCI),

Scott D Ramsey, PRINCIPAL_INVESTIGATOR, Fred Hutchinson Cancer Center

Study Record Dates

2029-06-30