REVELUTION-2: Relugolix+Abiraterone Acetate (AA) Versus Leuprolide+AA Cardiac Trial
Conditions
Recurrent Prostate Carcinoma, Stage III Prostate Cancer AJCC V8, Stage IVA Prostate Cancer AJCC V8Drugs
Abiraterone Acetate, Bicalutamide, Leuprolide, Prednisone, RelugolixSummary
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
- Bill Zheng
- 404-686-6856
- [email protected]
Principal Investigator
- Sagar A Patel, MD
Status
- RECRUITING
Contact Person
- Bill Zheng
- 404-686-6856
- [email protected]
Principal Investigator
- Sagar A Patel, MD
Status
- RECRUITING
Contact Person
- Sagar A. Patel, MD
- 404-686-4835
- [email protected]
Principal Investigator
- Sagar A Patel, MD
Status
- RECRUITING
Contact Person
- Bill Zheng
- 404-686-6856
- [email protected]
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 AcetateDescription:
Given abiraterone acetateDRUG:
BicalutamideDescription:
Given POPROCEDURE:
Biospecimen CollectionDescription:
Undergo blood sample collectionPROCEDURE:
Computed Tomography AngiographyDescription:
Undergo CCTADRUG:
LeuprolideDescription:
Given IM or SCDRUG:
PrednisoneDescription:
Given prednisoneRADIATION:
Radiation TherapyDescription:
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 AcetateDescription:
Given abiraterone acetatePROCEDURE:
Biospecimen CollectionDescription:
Undergo blood sample collectionPROCEDURE:
Computed Tomography AngiographyDescription:
Undergo CCTADRUG:
PrednisoneDescription:
Given prednisoneRADIATION:
Radiation TherapyDescription:
Undergo standard of care radiation therapyDRUG:
RelugolixDescription:
Given PO
Outcome Measures
Primary Outcome Measures
Incidence of ambulatory systolic blood pressure (BP) > 140 or diastolic > 90 (measurement on 2 separate days)
Need for new or escalated anti-hypertensive medication
Incidence of moderate-to-severe atherosclerosis of major coronary vessels
Secondary Outcome Measures
Total plaque volume
Pre-existing genomic alterations promoting inflammatory immunity and associated with cardiovascular disease
Castration rate
Sustained castration
Testosterone recovery
Timeline
Last Updated
February 21, 2025Start Date
October 21, 2024Today
May 12, 2025Completion Date ( Estimated )
July 1, 2029
Sponsors of this trial
Lead Sponsor
Emory UniversityCollaborating Sponsors
Pfizer, Sumitomo Pharma America, Inc., National Comprehensive Cancer Network, National Cancer Institute (NCI)