Investigator Initiated Trial to Further Evaluate the Safety and Efficacy of Trans-perineal Focal Laser Ablation of Localized Prostate Cancer Using High Frequency Micro-ultrasound Imaging

Stopped early · Not applicable

Conditions studied: Prostate Cancer, Low-risk or Favorable Intermediate Risk Prostate Cancer Who Are on an Active Surveillance Regimen

In brief

Trans-perineal focal laser ablation represents a promising alternative focal therapy option for patients with low-risk or favorable intermediate risk prostate cancer. FLA has been extensively utilized for over a decade in the treatment of PCa using different anatomical approaches. The proposed study differs from past ones in that a trans-perineal approach with reduced risk of infection will be used in contrast to the current trans-rectal approach. In addition, high frequency micro-ultrasound imaging will be used to enhance imaging and facilitate accurate needle placement and FLA of the index lesions. The aim of this study is to evaluate FLA as a potential optimal therapeutic intervention based on safety, ease of use, efficacy, and cost.1 FLA holds promise for the management of localized tumors. The combination of the trans-perineal focal laser ablation and micro-ultrasound imaging will enable targeted trans-perineal fusion laser induced thermal therapy of prostate cancer lesions. This approach offers significant potential advantages over traditional interventions including: * Improved dynamic ultrasound imaging of the lesion to be treated compared to traditional ultrasound techniques. * Enhanced ability to visualize and spare critical structures within the prostate, including the bladder neck, neurovascular bundle (NVB), urethral sphincter and organs in close proximity including the rectum. * Sparing these structures should translate into improved preservation of ejaculation, limited changes in sexual function and minimal transient incontinence following treatment.

Key facts

Study ID

NCT05826470

Run by

Genesis Research LLC

People needed

4

Starts

2023-05-30

Expected to finish

2024-12-05

Last updated by the study team

2024-12-10

Who can join

Age: 40 and older, up to 85. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Men between the ages of 40 and 85 years
• Ability to read, understand and agree/sign the patient informed consent in the English language.
• Serum PSA < 20 ng/ml
• AJCC clinical tumor stage T2b or less (according to digital rectal examination)
• Men with localized PCa (GG 1or 2, Gleason Score 7 or less) (Low or Favorable Intermediate Risk PCa) with an MR-image detected index lesion done within three months from the time of enrollment and visible on micro-ultrasound
• According to the decision of the investigator:
• Patient is suitable to undergo treatment with FLA
• Able to tolerate a procedure under local anesthesia
• Able to undergo Nitrous Oxide sedation
• Able to undergo MR
• has normal rectal anatomy
• Lesion Specificity:
• Unilateral, with cumulative lesion volumes not comprising more than 50 percent of the lobe as determined by MRI
• Lesion distances from the outer perimeter of the energy emitting zone of the diffuser to adjacent vital structures (bladder wall, rectal wall, neurovascular bundles, and urethra) must be ≥ 8mm
• Minimum distance to rectal wall and other sensitive structures ≥ 8mm

You may not qualify if…

• Previous prostate surgery
• Patients with recurrent prostate cancer
• Anticoagulant therapy
• Gleason Grade Group 3 PCa or higher
• Multifocal PCa other than Gleason Grade Group 1
• Locally advanced or metastatic PCa
• Prior or ongoing PCa treatment including surgery, radiation therapy, hormonal therapy or focal therapy
• Previous radiation of the pelvic region
• Intraprostatic calculus > 5mm
• Inability to tolerate a dorsal lithotomy position under Nitrous Oxide sedation for > 90 minutes
• ECOG Status ≥2
• Urethral Stenosis
• Prostate height > 5 cm anterior to posterior or a prostate volume >100 cc's

Where it is running

• Genesis Research LLC. — San Diego, California, United States

Full record on ClinicalTrials.gov

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