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Hormone Therapy
Hormone Therapy + Radiation for Prostate Cancer
N/A
Waitlist Available
Led By Stanley Liauw, MD
Research Sponsored by University of Chicago
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 years
Awards & highlights
All Individual Drugs Already Approved
Approved for 5 Other Conditions
No Placebo-Only Group
Summary
This trial is testing if taking hormone pills can improve the quality of life and survival rates for patients who need hormone-based treatment. The pills work by adjusting hormone levels in the body to help manage their condition.
Who is the study for?
Men aged 18+ with intermediate or high-risk prostate cancer who haven't had radical surgery, hormonal therapy, or certain other treatments for prostate cancer. They should have a life expectancy of at least 10 years and be able to give informed consent. Men with severe health issues like unstable angina, active infections needing IV antibiotics, liver problems, AIDS, or autoimmune diseases are excluded.
What is being tested?
The trial is testing if oral hormone therapies (Bicalutamide, Dutasteride, Finasteride) plus radiation improve quality of life and survival rates compared to standard care in men with prostate cancer. It's looking at how well patients do on these drugs versus the usual treatment.
What are the potential side effects?
Possible side effects from the hormone therapies may include breast tenderness/enlargement, hot flashes, reduced sex drive/erectile function; while radiation can cause fatigue, skin changes in treated area and urinary/bowel symptoms.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Quality of Life Was Measured by the Expanded Prostate Cancer Index Composite (EPIC) Hormonal Health-related Quality of Life Questionnaire
Secondary study objectives
Percentage of Participants Free From Biochemical Failure
Awards & Highlights
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Approved for 5 Other Conditions
This treatment demonstrated efficacy for 5 other conditions.
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Oral Androgen TherapyExperimental Treatment4 Interventions
Subjects will receive two oral hormonal drugs (bicalutamide with dutasteride or bicalutamide with finasteride)
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Radiation
2003
Completed Phase 2
~780
Finasteride
FDA approved
Bicalutamide
FDA approved
Dutasteride
FDA approved
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for prostate cancer, particularly hormone-sensitive types, focus on altering hormone levels to inhibit tumor growth. Androgen deprivation therapy (ADT) reduces androgen levels through surgical or medical means, such as LHRH agonists and antagonists, which lower testosterone.
Newer antiandrogens like enzalutamide block androgen receptors, while abiraterone inhibits androgen production. These treatments are vital as they target the hormonal pathways essential for prostate cancer cell growth, thereby slowing disease progression and improving patient outcomes.
Screening and hormonal therapy of localized prostate cancer shows major benefits on survival.
Screening and hormonal therapy of localized prostate cancer shows major benefits on survival.
Find a Location
Who is running the clinical trial?
University of ChicagoLead Sponsor
1,052 Previous Clinical Trials
758,965 Total Patients Enrolled
22 Trials studying Prostate Cancer
8,323 Patients Enrolled for Prostate Cancer
Stanley Liauw, MDPrincipal InvestigatorUniversity of Chicago
1 Previous Clinical Trials
17 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Oral Androgen Therapy
Awards:
This trial has 3 awards, including:- All Individual Drugs Already Approved - Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
- Approved for 5 Other Conditions - This treatment demonstrated efficacy for 5 other conditions.
- 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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