RECRUITING

REVELUTION-2: Relugolix+Abiraterone Acetate (AA) Versus Leuprolide+AA Cardiac Trial

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This phase III/IV trial compares the impact of leuprolide and abiraterone acetate (AA) versus relugolix and AA on the heart in hormone-naive patients with advanced prostate cancer receiving pelvic radiation therapy. Leuprolide is in a class of medications called gonadotropin-releasing hormone agonists (GNRHa). It prevents the body from making luteinizing hormone-releasing hormone (LHRH) and luteinizing hormone (LH). This causes the testicles to stop making testosterone (a male hormone) in men and may stop the growth of prostate tumor cells that need testosterone to grow. Abiraterone acetate, an androgen biosynthesis inhibitor, works by decreasing the amount of certain hormones in the body. Relugolix, a GNRH antagonist, works by decreasing the amount of testosterone produced by the body. This may slow or stop the spread of prostate tumor cells that need testosterone to grow. The use of hormone therapy with radiation therapy has been shown to improve survival, however, studies have suggested that the addition of hormone therapy may worsen heart (cardiac) disease and high blood pressure. In fact, studies have shown that the most common cause of death in prostate cancer patients is due to heart disease or heart attacks. Computed tomography (CT) scans create a series of detailed pictures of areas inside the body; the pictures are created by a computer linked to an x-ray machine. In this study, sophisticated cardiac CT images are used to take pictures of patients' heart and coronary arteries to help assess damage to the heart. Using cardiac CT and blood tests, this trial may help doctors determine which patients are at risk of cardiac disease when treated with combination hormone therapy, as well as the differential risk of leuprolide versus relugolix in combination with abiraterone acetate.

Official Title

Randomized Controlled Trial of Leuprolide Plus Abiraterone Acetate (AA) Versus Relugolix Plus AA for Advanced Prostate Cancer: the REVELUTION-2 Trial

Quick Facts

Study Start:2025-01-31
Study Completion:2029-07-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06650579

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:MALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Men ≥ 18 years old
  2. * Non-metastatic prostate cancer
  3. * Non-metastatic, biochemically recurrent prostate cancer
  4. * Plan to undergo curative-intent pelvic radiation therapy (photons or protons) with or without brachytherapy
  5. * Plan to undergo up to 24 months of combination androgen deprivation therapy (ADT) plus AA and prednisone
  1. * Metastatic prostate cancer requiring indefinitive ADT or chemotherapy
  2. * Prior exposure to androgen deprivation therapy
  3. * Prior exposure to chemotherapy, immunotherapy, or radiation therapy
  4. * History of cardiac bypass surgery or percutaneous coronary intervention
  5. * History of cardiac pacemaker or defibrillator

Contacts and Locations

Study Contact

Bill Zheng, BS
CONTACT
404-686-6856
bill.zheng@emory.edu

Principal Investigator

Sagar A Patel, MD
PRINCIPAL_INVESTIGATOR
Emory University Hospital/Winship Cancer Institute

Study Locations (Sites)

Emory Proton Therapy Center
Atlanta, Georgia, 30308
United States
Winship at Emory Midtown
Atlanta, Georgia, 30308
United States
Emory University Hospital/Winship Cancer Institute
Atlanta, Georgia, 30322
United States
Emory Saint Joseph's Hospital
Atlanta, Georgia, 30342
United States

Collaborators and Investigators

Sponsor: Emory University

  • Sagar A Patel, MD, PRINCIPAL_INVESTIGATOR, Emory University Hospital/Winship Cancer Institute

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-01-31
Study Completion Date2029-07-01

Study Record Updates

Study Start Date2025-01-31
Study Completion Date2029-07-01

Terms related to this study

Keywords Provided by Researchers

  • node-positive prostate cancer
  • advanced prostate cancer
  • very-high-risk prostate cancer

Additional Relevant MeSH Terms

  • Recurrent Prostate Carcinoma
  • Stage III Prostate Cancer AJCC V8
  • Stage IVA Prostate Cancer AJCC V8