RecruitingNot ApplicableNCT06223295

Effectiveness of Focal Therapy in Men With Prostate Cancer


Sponsor

Radboud University Medical Center

Enrollment

356 participants

Start Date

Feb 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

In the Netherlands, most men with prostate cancer (PCa) are treated with radical whole-gland treatment, i.e. prostatectomy or radiotherapy. The burden of complications such as incontinence and erectile dysfunction associated with radical treatment is considerable. A recent systematic review by our group has shown that focal therapy of PCa seems to reduce the burden of treatment side-effects in men with intermediate-risk disease, maintaining their quality of life without compromising oncological effectiveness. The costs of side effects that can be prevented are estimated at €5456 per patient, resulting in total expected cost savings of about €22 million per year in The Netherlands. Furthermore, exploration of the benefit-risk balance under patients showed that they are willing to sacrifice some survival for an improvement in quality of life (QoL). Focal therapy comprises a modern alternative to selectively treat a specific part of the prostate while preserving the rest of the gland. There is, however, a lack of high-quality evidence, and numerous papers therefore recommend to perform a multicenter randomized controlled trial (RCT). The RCT should have long-term follow-up, predefined assessment of cancer-specific and health-related QoL outcome measures, and economic evaluations to inform policymakers regarding cost-effectiveness. This RCT on focal therapy versus usual care is urgently needed to enable focal therapy to overgrow the experimental status, provide the evidence needed for guidelines, and make this available for selected patients who benefit from this strategy. Because of its promising results in other countries, focal therapy is increasingly requested by patients, but due to the lack of high-quality evidence, it is not reimbursed yet. This has been designated by both the PCa patient support group and physicians as a failure of both the market and the funding agencies. The investigators, therefore, aim to perform a high-quality multi-center RCT to provide the evidence needed to decide on reimbursement and implementation of focal therapy in patients with intermediate-risk, unilateral clinically localized PCa in the Netherlands.


Eligibility

Sex: MALEMin Age: 45 Years

Plain Language Summary

Simplified for easier understanding

This study is evaluating focal therapy — a targeted treatment that destroys only the cancerous part of the prostate rather than the whole gland — as an alternative to full surgery or radiation in men with intermediate-risk prostate cancer. **You may be eligible if...** - You are a man with intermediate-risk prostate cancer (Gleason score 7, meaning moderately aggressive) - Your PSA level is 20 ng/mL or below - Your cancer appears contained within the prostate (stage T2b or lower) - Your life expectancy is 10 years or more - You would normally be a candidate for radical surgery or full-dose radiation therapy - You have not had any previous prostate treatment **You may NOT be eligible if...** - You have low-grade or low-volume cancer that would typically be monitored rather than treated - You have high-risk prostate cancer (Gleason 8 or higher) or cancer extending outside the prostate - You have a cardiac pacemaker or metal stents in the prostate/urethra - You have significant kidney impairment - You cannot tolerate a rectal ultrasound 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

PROCEDUREFocal therapy

Focal therapy selectively treats a specific part of the prostate while preserving the rest of the gland in men with prostate cancer. Focal therapy with ultrasound ablation (HIFU/TULSA) or irreversible electroporation (IRE) followed by an intensive MRI follow-up scheme at 12, 24, 36, 48 and 60 months, prostate biopsy at 12 months (and also when indicated) and PSA monitoring

PROCEDUREUsual care

standard radical treatment; prostatectomy or radiotherapy with follow-up according international guidelines (PSA monitoring and imaging when indicated).


Locations(5)

Radboud University Medical Centre

Nijmegen, Gelderland, Netherlands

Hifu kliniek

Etten-Leur, North Brabant, Netherlands

Amsterdam UMC

Amsterdam, North Holland, Netherlands

Isala klinieken

Zwolle, Overijssel, Netherlands

St. Antonius hospital

Nieuwegein, Utrecht, Netherlands

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NCT06223295


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