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TERPS Trial for de Novo Oligometastic Prostate Cancer

RecruitingPhase 2

Phase 2 Randomized Total Eradication of Metastatic Lesions Following Definitive Radiation to the Prostate in de Novo oligometaStatic Prostate Cancer (TERPS) Trial

Who can join

Ages 18 and older · Men

Full eligibility criteria
Inclusion Criteria:

1. Patient must have at least one and up to three asymptomatic metastatic tumor(s) of the bone or soft tissue (with at least one bone metastasis) develop within the past 6-months that are seen on imaging. Up to five lesions are allowed on advanced functional imaging such as fluciclovine (Axumin), choline or PSMA PET-CT scan.

   1. CT or MRI scan within 6 months of enrollment
   2. Bone scan within 6 months of enrollment
   3. Fluciclovine (Axumin), choline, or PSMA PET-CT scan within 6 months of enrollment (PET-CT scan is reasonable for study entry imaging as an alternative to CT/MRI scan and bone scan)
2. Histologic confirmation of malignancy (primary or metastatic tumor).
3. Patient may have had prior systemic therapy and/or ADT associated with treatment within 9-months of enrollment.
4. PSA \> 0.5 but \<100.
5. Patient must be ≥ 18 years of age.
6. Patient must have a life expectancy ≥ 12 months.
7. Patient must have an ECOG performance status ≤ 2.
8. Patient must have the ability to understand and the willingness to sign a written informed consent document

Exclusion Criteria:

1. Castration-resistant prostate cancer (CRPC).
2. Prior radiation therapy to an overlapping site of a target lesion that would preclude further radiation therapy
3. Spinal cord compression or impending spinal cord compression.
4. Suspected pulmonary and/or liver metastases (greater \>10 mm in largest axis).
5. Patient receiving any other investigational agents.
6. Inability to receive any form of systemic therapy in the opinion of a treating medical oncologist .
7. Unable to lie flat during or tolerate PET/MRI, PET/CT or SABR.
8. No radiographical evidence of cranial metastasis.
9. Refusal to sign informed consent.

About the study

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.

What is being tested

Sponsor: University of Maryland, Baltimore · Participants: 122 · Started: Oct 18, 2022

Contact the study team

Official record on ClinicalTrials.gov — NCT05223803

Locations in the U.S.

CaliforniaUC San Diego Moores Cancer Center, La Jolla
KansasKU Medical Center- Cancer Center, Kansas City
MarylandMaryland Proton Treatment Center, Baltimore
UMMC, Baltimore
Upper Chesapeake Health, Bel Air
Central Maryland Radiation Oncology, Columbia
Baltimore Washington Medical Center, Glen Burnie
PennsylvaniaSidney Kimmel Cancer Center at Jefferson Health, Philadelphia
UPMC Hillman Cancer Center, Pittsburgh
VirginiaBon Secours Cancer Institute at St. Francis, Midlothian

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.