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Radium-223 + SABR for Prostate Cancer (RAVENS Trial)
Phase 2
Waitlist Available
Led By Phuoc Tran, M.D., Ph.D.
Research Sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patient must have an ECOG performance status ≤ 2
Histologic confirmation of malignancy (primary or metastatic tumor)
Must not have
PSMA-PET/MRI or PSMA-PET/CT scan within the past 6 months with results that demonstrate more disease lesions than baseline CT/Bone Scan
Patient receiving abiraterone and prednisone
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing whether adding Radium-223 to SABR treatment for men with oligometastatic prostate cancer improves progression-free survival.
Who is the study for?
Men over 18 with oligometastatic prostate cancer, treated primary tumor, PSA levels between 0.5-50, and at least one recent bone metastasis are eligible. They must have normal organ/marrow function and a life expectancy of over a year. Those with more than three years of ADT history or recent treatment aren't eligible.
What is being tested?
This Phase II trial compares the effectiveness of SABR alone versus SABR combined with Radium-223 in men with oligometastatic prostate cancer to see which is better for halting disease progression.
What are the potential side effects?
Potential side effects include radiation-related symptoms such as fatigue, skin reactions, nausea, and potential bone marrow suppression from Radium-223 leading to anemia or increased infection risk.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I can take care of myself and perform daily activities.
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My cancer diagnosis was confirmed through tissue examination.
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My blood tests show normal white blood cells, platelets, and hemoglobin levels.
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I am 18 years old or older.
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My initial cancer was treated with surgery or radiation.
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I have 1-3 painless bone or soft tissue tumors developed in the last 6 months, each not larger than 5.0 cm.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My recent scans show more cancer spots than before.
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I am currently taking abiraterone and prednisone.
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I have or am at risk of having pressure on my spinal cord.
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I have suspected lung or liver cancer spread larger than 10 mm.
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My prostate cancer is not responding to hormone therapy.
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I cannot lie flat for scans or certain cancer treatments.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Progression-free survival
Secondary study objectives
ADT-free survival
Local control at 12 months
Quality of Life as assessed by Pain Severity and Pain Interference using the Brief Pain Inventory
+4 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Radium-223 and SABRExperimental Treatment2 Interventions
First radium-223 infusion will be within two weeks of SABR
Group II: SABRActive Control1 Intervention
SABR(1-5 fractions) will be administered for all men
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Radium-223
2023
Completed Phase 2
~100
Find a Location
Who is running the clinical trial?
BayerIndustry Sponsor
2,274 Previous Clinical Trials
25,514,628 Total Patients Enrolled
44 Trials studying Prostate Cancer
26,911 Patients Enrolled for Prostate Cancer
Department of Defense Congressionally Directed Medical Research ProgramUNKNOWN
2 Previous Clinical Trials
576 Total Patients Enrolled
Sidney Kimmel Comprehensive Cancer Center at Johns HopkinsLead Sponsor
570 Previous Clinical Trials
33,166 Total Patients Enrolled
57 Trials studying Prostate Cancer
3,364 Patients Enrolled for Prostate Cancer
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My recent scans show more cancer spots than before.I have suspected lung or liver cancer spread larger than 10 mm.My prostate cancer is progressing quickly.I have had hormone therapy or other treatments for my prostate cancer.I am currently taking abiraterone and prednisone.You are currently taking any other medications that are still being tested.I have or am at risk of having pressure on my spinal cord.I can take care of myself and perform daily activities.My cancer diagnosis was confirmed through tissue examination.My blood tests show normal white blood cells, platelets, and hemoglobin levels.I have had hormone therapy for cancer, but not in the last 6 months and no more than 3 years total.I am 18 years old or older.My prostate cancer is not responding to hormone therapy.I can understand and am willing to sign the consent form.I cannot lie flat for scans or certain cancer treatments.My initial cancer was treated with surgery or radiation.I have had previous treatment for my prostate cancer.I have 1-3 painless bone or soft tissue tumors developed in the last 6 months, each not larger than 5.0 cm.
Research Study Groups:
This trial has the following groups:- Group 1: Radium-223 and SABR
- Group 2: SABR
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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