Androgen Deprivation Therapy for Prostate Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests how well a short course of the medication relugolix works with imaging to detect prostate cancer that might have spread, especially in high-risk cases. Relugolix reduces testosterone, which can help identify more cancer cells during special imaging scans (PSMA PET/CT). The trial divides participants into three groups, each receiving relugolix for different lengths of time before imaging and surgery. Men with high-risk prostate cancer, such as those with aggressive forms or high PSA levels, might be suitable for this study. As a Phase 2 trial, this research measures the treatment's effectiveness in an initial, smaller group, offering a chance to contribute to important findings.
Do I need to stop taking my current medications for the trial?
The trial does not specify if you need to stop taking your current medications. However, you cannot have had chemotherapy within 2 weeks before joining, and you cannot be on androgen deprivation therapy or pelvic radiation. It's best to discuss your specific medications with the trial team.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that relugolix is generally well-tolerated by patients. In a study on its use for prostate cancer, only 2.9% of patients experienced major heart problems, compared to 6.2% with leuprolide. This suggests relugolix might pose a lower risk of heart issues. Another study found no new safety concerns when relugolix was combined with radiotherapy. These findings offer some reassurance about the safety of relugolix, but ongoing trials will continue to monitor for any issues.12345
Why are researchers excited about this trial's treatments?
Researchers are excited about relugolix for prostate cancer because it offers a new approach to androgen deprivation therapy (ADT). Unlike traditional ADT options like leuprolide, which are administered via injections and can take weeks to lower testosterone levels, relugolix is an oral medication that can rapidly reduce testosterone levels in just a few days. This faster action could potentially lead to quicker symptom relief and may improve the timing and effectiveness of subsequent treatments, like surgery. Additionally, as a non-invasive oral treatment, relugolix offers a more convenient alternative for patients compared to injectable therapies.
What evidence suggests that this trial's treatments could be effective for prostate cancer?
Research has shown that relugolix effectively treats prostate cancer by lowering testosterone levels, which helps slow cancer cell growth. In clinical studies, over 98% of patients using relugolix achieved very low testosterone levels, crucial for controlling prostate cancer. It acts quickly and maintains these low levels in patients with both early-stage and advanced prostate cancer. This trial will test different durations of relugolix treatment, with participants receiving it for 5, 10, or 15 days. This treatment is promising because it targets hormones that promote cancer growth. Additionally, relugolix might improve the ability of imaging tests to detect smaller cancer areas in the body.35678
Who Is on the Research Team?
Jack R. Andrews, MD
Principal Investigator
Mayo Clinic
Are You a Good Fit for This Trial?
Men over 18 with high or very high risk prostate cancer confirmed by biopsy, who have not started treatment. They must be relatively healthy (ECOG PS 0-2), have normal blood counts, and testosterone levels above a certain threshold. Participants are required to use condoms and cannot donate semen during the trial.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive flotufolastat F 18 and undergo PET/CT on day 0, followed by relugolix orally once daily for 5, 10, or 15 days depending on the arm. A second PET/CT is performed on the last day of relugolix treatment.
Surgery
Participants undergo robotic radical prostatectomy with pelvic lymph node dissection within 90 days of the second PET/CT scan.
Follow-up
Participants are monitored for safety and effectiveness after treatment, including the incidence of adverse events.
What Are the Treatments Tested in This Trial?
Interventions
- Relugolix
Find a Clinic Near You
Who Is Running the Clinical Trial?
Mayo Clinic
Lead Sponsor