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

Clinicaltrials.gov ID: NCT06650579
db-list-check Status RECRUITING
b-loader Phase PHASE3
b-people Age ≥ 18 Years
b-bullseye-arrow Enrollments 72

Conditions

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

Drugs

Abiraterone Acetate, Bicalutamide, Leuprolide, Prednisone, Relugolix

Summary

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.

Detailed Description

PRIMARY OBJECTIVE:

I. Measure cardiovascular outcomes between combination gonadotropin releasing hormone agonist (GNRHa, i.e. leuprolide) plus abiraterone acetate (AA) versus gonadotropin releasing hormone antagonist (GNRH-antagonist, i.e. relugolix) plus AA in men with advanced prostate cancer receiving definitive radiation therapy.

SECONDARY OBJECTIVES:

I. Identify genomic alterations that predispose an individual to enhanced cardiovascular (CV) toxicity following hormone therapy with leuprolide or relugolix in combination with abiraterone acetate.

II. Evaluate serum testosterone kinetics during and after treatment with combination leuprolide+AA versus relugolix+AA.

OUTLINE: Patients are randomized to 1 of 2 arms.

ARM I: Patients receive leuprolide intramuscularly (IM) or subcutaneously (SC) injection every 3 to 6 months plus oral AA with prednisone daily for up to 24 months in the absence of disease progression or unacceptable toxicity. Patients also undergo standard of care radiation therapy. Patients may also receive bicalutamide orally (PO) once daily (QD) on days 21-30 with first injection of leuprolide at the discretion of the treating provider. All patients undergo pre-treatment and 12-month coronary computed tomography angiography (CCTA) and blood sample collection.

ARM II: Patients receive oral relugolix PO daily plus oral AA with prednisone daily for up to 24 months in the absence of disease progression or unacceptable toxicity. Patients also undergo standard of care radiation therapy. All patients undergo pre-treatment and 12-month CCTA and blood sample collection.

After completion of study treatment, patients are followed up at 30 and 60 days for serum testosterone measurement.

Locations

4 locations Found with status Recruiting

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Sagar A Patel, MD

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Sagar A Patel, MD

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Sagar A Patel, MD

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Sagar A Patel, MD

Eligibility Criteria

Inclusion Criteria:

* Men ≥ 18 years old
* Non-metastatic prostate cancer
* Non-metastatic, biochemically recurrent prostate cancer
* Plan to undergo curative-intent pelvic radiation therapy (photons or protons) with or without brachytherapy
* Plan to undergo up to 24 months of combination androgen deprivation therapy (ADT) plus AA and prednisone

Exclusion Criteria:

* Metastatic prostate cancer requiring indefinitive ADT or chemotherapy
* Prior exposure to androgen deprivation therapy
* Prior exposure to chemotherapy, immunotherapy, or radiation therapy
* History of cardiac bypass surgery or percutaneous coronary intervention
* History of cardiac pacemaker or defibrillator

Study Plan

Arm I (leuprolide plus abiraterone acetate/prednisone)

EXPERIMENTAL

Patients receive leuprolide IM or SC injections every 3 to 6 months plus oral abiraterone acetate (AA) with prednisone daily for up to 24 months in the absence of disease progression or unacceptable toxicity. Patients also undergo standard of care radiation therapy.

  • DRUG:

    Abiraterone Acetate

    Description:

    Given abiraterone acetate
  • DRUG:

    Bicalutamide

    Description:

    Given PO
  • PROCEDURE:

    Biospecimen Collection

    Description:

    Undergo blood sample collection
  • PROCEDURE:

    Computed Tomography Angiography

    Description:

    Undergo CCTA
  • DRUG:

    Leuprolide

    Description:

    Given IM or SC
  • DRUG:

    Prednisone

    Description:

    Given prednisone
  • RADIATION:

    Radiation Therapy

    Description:

    Undergo standard of care radiation therapy

Arm II (relugolix + abiraterone acetate/prednisone)

EXPERIMENTAL

Patients receive oral relugolix daily plus oral abiraterone acetate (AA) with prednisone daily for up to 24 months in the absence of disease progression or unacceptable toxicity. Patients also undergo standard of care radiation therapy.

  • DRUG:

    Abiraterone Acetate

    Description:

    Given abiraterone acetate
  • PROCEDURE:

    Biospecimen Collection

    Description:

    Undergo blood sample collection
  • PROCEDURE:

    Computed Tomography Angiography

    Description:

    Undergo CCTA
  • DRUG:

    Prednisone

    Description:

    Given prednisone
  • RADIATION:

    Radiation Therapy

    Description:

    Undergo standard of care radiation therapy
  • DRUG:

    Relugolix

    Description:

    Given PO

Outcome Measures

Primary Outcome Measures

Incidence of ambulatory systolic blood pressure (BP) > 140 or diastolic > 90 (measurement on 2 separate days)

Time Frame: At baseline and up to 12 months

Need for new or escalated anti-hypertensive medication

Time Frame: At baseline and up to 12 months

Incidence of moderate-to-severe atherosclerosis of major coronary vessels

Time Frame: From month 0 to month 12

Secondary Outcome Measures

Total plaque volume

Time Frame: From month 0 to month 12

Pre-existing genomic alterations promoting inflammatory immunity and associated with cardiovascular disease

Time Frame: At baseline

Castration rate

Time Frame: At study days 7, 30 and 90

Sustained castration

Time Frame: At months 6 and 12

Testosterone recovery

Time Frame: At day 30 and/or day 90 following completion of androgen deprivation therapy

Timeline

  • Last Updated
    February 21, 2025
  • Start Date
    October 21, 2024
  • Today
    May 12, 2025
  • Completion Date ( Estimated )
    July 1, 2029

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