Status:
ACTIVE_NOT_RECRUITING
Enzalutamide With or Without Radium Ra 223 Dichloride in Patients With Metastatic, Castration-Resistant Prostate Cancer
Lead Sponsor:
University of Southern California
Collaborating Sponsors:
National Cancer Institute (NCI)
Conditions:
Castration-Resistant Prostate Carcinoma
Prostate Carcinoma Metastatic in the Bone
Eligibility:
MALE
18+ years
Phase:
PHASE2
Brief Summary
This randomized phase II trial studies how well enzalutamide with or without radium Ra 223 dichloride in treating patients with castration-resistant prostate cancer that has spread to other places in ...
Detailed Description
PRIMARY OBJECTIVES: I. To evaluate changes in prostate cancer bone involvement induced by enzalutamide alone or in combination with radium Ra 223 dichloride (radium 223), specifically extent of prost...
Eligibility Criteria
Inclusion
- Men with metastatic, castration resistant prostate cancer involving the bone, which is symptomatic or asymptomatic
- Castration resistance will be defined as the development of disease progression, defined as one of the following:
- Rising PSA x 2 values \>= 2 weeks apart; minimum absolute PSA value 2 ng/mL
- Radiographic progression, with at least 1 new site of metastasis
- Symptomatic progression (ex: increase in pain despite stable imaging) AND despite ongoing luteinizing hormone-releasing hormone (LHRH) therapy OR testosterone level \< 50
- Men must have osseous metastases, but the presence of visceral metastases will not exclude patients from participation
- Prior external beam radiation therapy (\> 4 weeks prior to enrollment) for palliation of osseous metastatic disease is allowed, provided there is at least one osseous metastasis which has not been irradiated and which can be biopsied
- No prior docetaxel or cabazitaxel chemotherapy for metastatic castration-resistant prostate cancer (mCRPC) (men treated with prior docetaxel administered as up-front therapy with androgen deprivation therapy \[ADT\] \> 6 months ago will be eligible); prior abiraterone is allowed
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-1
- Hemoglobin \>= 9.5 g/dL
- Absolute neutrophil count \>= 1,500
- Platelets \>= 100,000
- Total bilirubin within normal institutional limits
- Creatinine clearance (calculated or measured) \> 30 mL/min
- At least one risk factor predicting higher likelihood of bone marrow sample yield: elevated alkaline phosphatase, low hemoglobin, or elevated lactate dehydrogenase (LDH)
- Ability to understand and the willingness to sign a written informed consent
Exclusion
- Prior treatment with docetaxel or cabazitaxel for mCRPC
- Prior treatment with ARN-509 or enzalutamide (there is a grace period for men who wish to enroll and who have recently started enzalutamide for the first time but have taken less than 15 days of therapy)
- Concurrent use of androgen deprivation therapy aside from LHRH agonist or antagonist (i.e. bicalutamide, flutamide, nilutamide, abiraterone, ketoconazole, estrogen); there will be a 2 week wash-out period from the last dose of any of these agents until the first dose of enzalutamide on study; patients who have just started enzalutamide for fewer than 5 doses prior to enrollment in the trial are still considered eligible and not subject to wash-out
- Concurrent oral corticosteroid use aside from adrenal replacement, or use of other immunosuppressive agents (ex: infliximab); topical or inhaled steroids will be allowed
- Received systemic therapy with radionuclides (e.g., strontium-89, samarium- 153, rhenium-186, or rhenium-188, or radium Ra 223 dichloride) for the treatment of bony metastases
- History of seizures except for remote with specific etiology which has resolved (ex: alcohol induced seizure); transient ischemic attack (TIA) or cerebrovascular accident (CVA) within last 6 months
- Known untreated central nervous system (CNS) metastases; leptomeningeal disease will be an absolute exclusion criterion due to limited life expectancy
- Chronic diarrhea \> grade 1, or a diagnosis of Crohn?s or ulcerative colitis
- Known hepatitis (hep) B or C, or known cirrhosis (screening for viral hepatitis is not required)
- Uncontrolled intercurrent illness such as infection, symptomatic congestive heart failure, unstable angina pectoris, or psychiatric illness which would limit compliance with study requirements
- Imminent spinal cord compression based on clinical findings and/or magnetic resonance imaging (MRI); treatment should be completed for spinal cord compression
Key Trial Info
Start Date :
November 21 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 21 2027
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT03344211
Start Date
November 21 2018
End Date
November 21 2027
Last Update
November 17 2025
Active Locations (3)
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1
City of Hope
Duarte, California, United States, 91010
2
USC / Norris Comprehensive Cancer Center
Los Angeles, California, United States, 90033
3
Cedars Sinai Medical Center
Los Angeles, California, United States, 90048