Purpose

This study will assess whether DNA released by kidney cancer into the blood stream and urine of patients can be used to monitor tumor burden and tumor response to treatment in patients receiving immunotherapy

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Renal Cell Carcinoma with clear cell component - Stage IV - Receiving IO-containing regimen - Measurable disease per RECIST 1.1

Exclusion Criteria

  • Active cancer (exclusion criteria only for healthy patient cohort)

Study Design

Phase
Study Type
Observational
Observational Model
Case-Only
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
RCC with clear cell component
  • Other: Blood collection
    20-40 mL of blood to extract cell free DNA
  • Other: Urine collection
    up to 15 mL of urine to extract cell free DNA
Healthy Volunteer (no longer recruiting)
  • Other: Blood collection
    20-40 mL of blood to extract cell free DNA
  • Other: Urine collection
    up to 15 mL of urine to extract cell free DNA

Recruiting Locations

Vanderbilt University Medical Center
Nashville, Tennessee 37232
Contact:
Scott Haake, MD
615-936-8422
scott.haake@vumc.org

Tennessee Valley Health Care System
Nashville, Tennessee 37212
Contact:
Scott Haake, MD
615-936-8422
scott.haake@vumc.org

More Details

Status
Recruiting
Sponsor
Vanderbilt-Ingram Cancer Center

Study Contact

Scott Haake, MD
615-936-8422
scott.haake@vumc.org

Detailed Description

Primary Objective: - Evaluate tumor cell free (cf)DNA as a dynamic marker of response to immuno-oncology (IO) therapy Exploratory Objective: - Collect data on somatic mutations in cfDNA to gain insight into the biology of IO-responders and -non-responders

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.