Prostate radiation (XRT)
RadiationBoth arms will receive prostate radiation. Multiple treatment regimens are allowed per protocol.
NCT Number: NCT05223803
This research is being done to see if we can improve the outcome of prostate cancer patients who present with metastatic lesions at initial diagnosis.
Interested in participating?
Request Info18 year and older
Male
Interventional
Phase 2
UC San Diego Moores Cancer Center, La Jolla, California, United States
This study will compare the effects, good and/or bad, of using the standard of care treatment (systemic therapy + primary prostate radiation) compared to standard of care treatment plus stereotactic ablative radiation therapy (SABR) to metastatic lesions for prostate patients. The researchers are also trying to learn if the addition of SABR will affect recurrence rates. Presence of circulating tumor cells, gut bacteria, and quality of life will be assessed for both groups.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Both arms will receive prostate radiation. Multiple treatment regimens are allowed per protocol.
All systemic therapy is provided as best prescribed for patient per their medical oncologist.
SABR is delivered to those randomized to Arm 2.
Time frame: 2 years
Cross-over to the SABR MDT is allowed following failure.
Time frame: 5 years
Adverse events will be assessed at baseline, on treatment visit, and follow-up visit.
Time frame: 1 year
Time frame: 5 years
Progression will be assessed for time to locoregional progression, time to distant progression, time to new metastasis, radiographic progression-free survival and duration of response after randomization to best systemic therapy (BST) and primary prostate radiation (XRT) versus BST, XRT and stereotactic ablative radiation therapy (SABR) metastasis-directed therapy (MDT).
Time frame: 5 years
EPIC quality of life tool will be used to assess quality of life following treatment. This survey will be completed at baseline and during follow-up visits. Averages will be taken for each section in the survey (Urinary Function, Bowel Function, Sexual Function, and Hormonal function).
Contact information is provided by the study sponsor or research team.
Nicole Helie
CONTACT
Zaker Rana, MD
CONTACT
University of Maryland, Baltimore
Other
Phase 2 Randomized Total Eradication of Metastatic Lesions Following Definitive Radiation to the Prostate in de Novo oligometaStatic Prostate Cancer (TERPS) Trial
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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