RecruitingNot ApplicableNCT04549688

Active Surveillance Plus (AS+): High-intensity Focused Ultrasound (HIFU) in Patients With Localized Prostate Cancer

Active Surveillance Plus (AS+): Local Tumor Control With High-intensity Focused Ultrasound (HIFU) in Patients With Localized Prostate Cancer


Sponsor

The Hospital of Vestfold

Enrollment

250 participants

Start Date

Sep 1, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

PSA (Prostate-specific antigen) testing has significantly increased the number of men diagnosed with prostate cancer (PCa) and especially patients with low and intermediate risk disease. The effect of radical treatment (treatment of the entire prostate gland) in these risk groups is disputable while the risk of adverse effects, with erectile dysfunction and urinary incontinence, is not. Active surveillance (AS) has been developed as an alternative to radical treatment with the aim of avoiding or delaying radical treatment by closely monitoring for signs of tumor progression. Active surveillance is regarded as the treatment of choice for low-risk prostate cancer. Focal therapy may have a crucial role in improving active surveillance protocols for patients with intermediate localized prostate cancer. Focal eradication of the index-tumor may delay or avoid indefinitely radical treatment for this patient group while significantly reducing treatment-related side effects. Improved MRI-diagnostics and MRI/ ultrasound fusion technology have optimized tumor mapping and classification and this in turn has made partial treatment of the prostate a feasible treatment option. This study is a prospective cohort study. Patients with intermediate (high-risk) localized PCa and a visible index tumor will be treated with high-intensity focused ultrasound (HIFU). The aim of the study is to show that there is a significant effect of focal treatment on surveillance biopsies and a reduced conversion to radical treatment, without compromising survival outcomes compared to historical controls (retrospective cohort). A cohort from the more than 450 patients included in the local AS-protocol with MRI at Vestfold hospital trust since 2009 will serve as controls.


Eligibility

Sex: MALEMin Age: 18 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether using High-Intensity Focused Ultrasound (HIFU) — a non-invasive technique that uses sound waves to destroy prostate tissue — alongside active surveillance (close monitoring without immediate treatment) is as safe and effective as surgery or radiation for men with low-to-intermediate risk localized prostate cancer. **You may be eligible if...** - You are between 55 and 80 years old - You have localized prostate cancer that has not spread to lymph nodes or other organs - Your Gleason score and PSA level are within the acceptable ranges for your age group - Your life expectancy is greater than 10 years - You have not previously received treatment for prostate cancer **You may NOT be eligible if...** - You have already had treatment for prostate cancer (including hormone therapy in the past 6 months) - You have had prior pelvic radiation - You have an active urinary tract infection - Your risk of lymph node involvement is high (for patients under 75) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREhigh-intensity focused ultrasound, HIFU

see above


Locations(1)

Vestfold Hospital Trust (Hospital of Vestfold)

Tønsberg, Vestfold, Norway

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NCT04549688


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