Prostate Cancer Clinical Trials

Find Prostate Cancer Clinical Trials Near You

Seeing the Unseen: ¹⁸F-PSMA-1007 PET-CT-Directed Focal Therapy for MRI-Invisible Prostate Cancer (The FOCUS-PSMA Study)

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Multiparametric magnetic resonance imaging (mpMRI) is the standard imaging modality for prostate cancer diagnosis and focal therapy planning. However, 10-20% of clinically significant prostate cancers (csPCa) are not visible on mpMRI (PI-RADS 1-2). These MRI-invisible lesions, typically identified only on systematic biopsy, are currently not targetable by MRI-guided focal therapy, leaving patients with the choice between whole-gland radical treatment or active surveillance. This prospective, multi-centre, single-arm phase II trial investigates whether pelvis-only ¹⁸F-PSMA-1007 positron emission tomography-computed tomography (PET-CT) can identify MRI-invisible csPCa and serve as the therapeutic navigation tool for focal ablation. Men aged ≥50 years with localized, intermediate-risk prostate cancer (ISUP Grade Group 2-3) and at least one MRI-invisible csPCa focus undergo a PET-CT. If a PET-avid lesion corresponds anatomically to the MRI-invisible biopsy-positive site, the patient receives focal therapy using an energy modality (targeted microwave ablation, high-intensity focused ultrasound, or irreversible electroporation) selected based on tumour anatomy, guided by organ-based tracking. The primary endpoint is the absence of csPCa (Grade Group ≥2) on 6-month targeted biopsy of all treated zones. Secondary endpoints include out-of-field recurrence, functional outcomes, and safety. The study requires 45 treated patients (total enrolment \ 60) across two Hong Kong centres and will be completed within 3 years.

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 50
Healthy Volunteers: f
View:

• Men aged ≥50 years

• Life expectancy \>10 years

• Histologically confirmed localized prostate cancer, ISUP Grade Group 2 or 3

• At least one clinically significant cancer focus (≥1 systematic biopsy core with Grade Group 2-3) that is MRI-invisible, defined as:

• \- The corresponding sextant/region on mpMRI (performed within 6 months) shows PI-RADS v2.1 score 1 or 2, or no identifiable lesion that could account for the positive biopsy

• Total of 1-2 discrete cancer foci (MRI-visible + PET-detected MRI-invisible) on study entry, with each MRI-visible focus having maximum diameter ≤15 mm on mpMRI

• Organ-confined disease on mpMRI and no evidence of seminal vesicle invasion or lymph node/distant metastasis

• Serum PSA \<20 ng/mL

• Able to provide informed consent

Locations
Other Locations
Hong Kong Special Administrative Region
Queen Mary Hospital
RECRUITING
Hong Kong
Contact Information
Primary
Shung Lai John Leung, MBBS, FRCSEd, FCSHK, FHKAM
jslleung@hku.hk
+852 2255 4852
Time Frame
Start Date: 2026-08-20
Estimated Completion Date: 2029-11-30
Participants
Target number of participants: 60
Treatments
Experimental: PET-Directed Focal Therapy
Patients with MRI-invisible csPCa who demonstrate a corresponding PET-avid lesion on ¹⁸F-PSMA-1007 PET-CT proceed to focal therapy. The ablative modality (targeted microwave ablation, high-intensity focused ultrasound, or irreversible electroporation) is selected by the treating urologist based on tumour location, anatomical constraints, and the known performance characteristics of each technology. All treatments are performed transperineally under organ-based tracking (OBT) navigation using the Koelis Trinity® platform, which fuses the PET-CT dataset with real-time transrectal ultrasound. Treatment covers the PET-positive MRI-invisible lesion and any concurrent MRI-visible lesions with a 5-10 mm intraprostatic margin, while preserving a ≥5 mm safety distance from the sphincter, rectum, and neurovascular bundles when clinically desired.
Related Therapeutic Areas
Sponsors
Collaborators: Queen Mary Hospital, Hong Kong
Leads: The University of Hong Kong

This content was sourced from clinicaltrials.gov