A Phase-II, Randomized, Assessor-Blind, Controlled Trial Comparing the Occurrence of Cardiovascular Events in Patients With Prostate Cancer and Cardiovascular Risk Factors Receiving Degarelix or GnRH Agonist
Overview
- Phase
- Phase 2
- Intervention
- Degarelix
- Conditions
- Hormone Sensitive Prostate Cancer
- Sponsor
- Rabin Medical Center
- Enrollment
- 80
- Locations
- 1
- Primary Endpoint
- time to first cardiovascular event
- Last Updated
- 6 years ago
Overview
Brief Summary
The purpose of this study is to test if the use of Degarelix for 1 year associated with a lower rate of cardiovascular toxicity compared to Gonadotropin-releasing hormone (GnRH) agonists in patients with advanced prostate cancer and cardiovascular risk factors, receiving combination therapy of Androgen deprivation therapy (ADT) and second line hormonal or chemotherapy?
Detailed Description
Study design: Randomized phase-2, open label superiority study of the use of ADT combined with second line hormonal or chemotherapy in men with advanced prostate cancer and pre-existing cardiovascular risks. Study population: Subjects with pre-existing cardiovascular risk with locally advanced or metastatic prostate cancer and scheduled to start ADT in combination with either second line hormonal or chemotherapy. We will exclude patients with use of ADT 6 months prior to randomization. Intervention- Two initial loading doses of 120mg Degarelix for 1 month followed by 80mg monthly for eleven additional months. Control- GnRH agonist at the discretion of the treating Urologist/Oncologist for 1 year. Study Time line- The intervention phase will be for one year. During this year, follow-up visits will occur every 3 months. At each visit, we will assess the occurrence of cardiac-related events. In addition, Protein-specific Antigen (PSA) test will be performed each visit. At baseline, 3, 6 and 12 months cardiac biomarkers and lab measurements will be taken. Echocardiogram will be performed at baseline, 6, 9 and 12 months. In addition, cardio-vascular related events and hospitalizations will be monitored for additional 5 years. Primary endpoint: To compare time to first cardiovascular event of patients with advanced prostate cancer treated for one year with Degarelix vs. GnRH agonist. This will be a composite outcome composed of: Death, Cerebrovascular accident (CVA), Myocardial infarction (MI), Transient ischemic attack (TIA), cardiac emergency room visits, heart catheterization. Secondary endpoints: To compare time to first major adverse cardiovascular and cerebrovascular event (MACCE)- (Death, CVA, MI, heart catheterization with stent) as estimated by the cumulated probability at the 1-year timepoint of patients with advanced prostate cancer treated for one year with Degarelix vs. LHRH agonist. To compare cardiovascular biomarker levels of patients with advanced prostate cancer treated with Degarelix vs. GnRH agonist. To compare change in cardiac function as measured by Echocardiography in 6,9 and 12 months. Study impact- This study has the potential to cause a paradigm shift. If we indeed demonstrate that Degarelix is associated with less cardiovascular toxicity with clinical significance, we expect that most urologist, as well as patients, will prefer Degarelix over all other ADT.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Locally advanced high-risk prostate cancer OR metastatic prostate cancer patients.
- •Patients are scheduled to receive a combination of either
- •primary ADT for 12 months + either chemotherapy with docetaxel OR
- •primary ADT for 12 months + second line hormonal treatment with abiraterone/ enzalutamide/ apalutamide
- •Patients with a medical history of either of the following:
- •Myocardial infarction
- •Ischaemic or haemorrhagic cerebrovascular conditions
- •Arterial embolic and thrombotic events
- •Ischaemic heart disease
- •Prior coronary artery or iliofemoral artery revascularization (percutaneous or surgical procedures)
Exclusion Criteria
- •Prior use of ADT in past 6 months prior to randomization. We will, however, allow prior use of anti-androgens such as Casodex, Chimax, Drogenil, and Cyprostat.
- •Known allergic reaction to Degarelix.
- •Any psychological, familial, sociological or geographical situation potentially hampering compliance with the study protocol and follow-up schedule.
Arms & Interventions
Degarelix
GnRH Antagonist
Intervention: Degarelix
GnRH-agonist
GnRH Agonist
Intervention: GnRH agonist
Outcomes
Primary Outcomes
time to first cardiovascular event
Time Frame: 1 year
To compare time to first cardiovascular event as estimated by the cumulated probability at the 1-year time-point of patients with advanced prostate cancer treated for one year with Degarelix vs. GnRH agonist. This will be a composite outcome composed of: Death, CVA, MI, TIA, cardiac emergency room visits, heart catheterization.
Secondary Outcomes
- time to first MACCE event(1 year)
- cardiac echocardiography(1 year)
- Hormonal Profile(1 year)
- NTproBNP levels(1 year)
- Adverse events(1 year)
- BMI(1 year)
- Quality of life: FACT-P questionnaire(1 year)
- Glucose profile(1 year)
- Cholesterol levles(1 year)
- PSA levles(1 year)