RecruitingNCT05344235

Observational Study on Extreme Hypofractionation for Localized Prostate Cancer


Sponsor

Universitaire Ziekenhuizen KU Leuven

Enrollment

246 participants

Start Date

Apr 25, 2022

Study Type

OBSERVATIONAL

Conditions

Summary

Radiotherapy (RT) is an established treatment option for localized prostate cancer (PCa), with cure rates similar to those of radical prostatectomy. In the last decade, conventionally fractionated RT (1.8-2.0 Gy per fraction to 78-80 Gy) has been replaced by moderately hypofractionated RT (2.3-3.65 Gy per fraction to 56-70 Gy). The rationale behind this change is the scientific level 1 evidence that a higher dose per fraction may improve the cost-benefit of RT due to the specific radiobiology of PCa (a lower alpha/beta than that of adjacent healthy tissues). Additionally, there is a practical advantage both for patients and the radiation department due to a reduced number of fractions. More recently, extreme hypofractionation or stereotactic body radiotherapy (SBRT) (7-9.5 Gy per fraction to 36-43 Gy in 4-7 fractions) has been introduced as RT modality, and proved to be an effective and safe treatment option for patients with low and intermediate clinically-localized PCa, with similar incidence of late toxicity and 5-year disease free survival outcomes when compared to hypofractionated and conventional radiotherapy regimens. International guidelines endorse extreme hypofractionated SBRT as routine treatment option for low and intermediate risk PCa patients. For high-risk prostate cancer, preliminary results of ongoing prospective studies are promising, but these data are not yet mature enough to recommend extreme hypofractionated SBRT in high-risk prostate cancer. Upon this, ongoing prospective trials handle strict eligibility criteria hereby selecting patients with few comorbidities. This may not necessarily fully reflect the real life patient population. Indeed, patients with a large prostate size, a history of transurethral resection of the prostate (TURP), or 'significant' urinary baseline symptoms may be at risk for experiencing increased toxicity. Based on this concern, these patients were excluded from ongoing clinical trials. However, whether these patients will really develop more toxicity, is a theoretical concern, not yet based on clinical evidence. It is our hypothesis that using modern radiotherapy such as volumetric arc therapy (VMAT) and image-guided radiotherapy (IGRT) - both standard technologies at the Radiation-Oncology department in Leuven University Hospitals - extreme hypofractionated SBRT can be successfully implemented in the treatment of intermediate risk and a select group of high-risk PCa patients and/or patients with pre-existing urinary morbidity.


Eligibility

Sex: MALE

Plain Language Summary

Simplified for easier understanding

This observational study is tracking outcomes of men with intermediate or high-risk localized prostate cancer who receive extreme hypofractionation — a type of radiation treatment that delivers a high dose in very few sessions (typically 5 sessions instead of 40+) — to assess effectiveness and side effects in real-world practice. **You may be eligible if...** - You are a man aged 18 or older - You have biopsy-confirmed prostate cancer confined to the prostate - Your cancer is intermediate or high risk (Gleason score ≥7, clinical stage cT2a or higher, or multiple risk factors) - There is no evidence of cancer spread beyond the prostate - You had an MRI of the prostate within 90 days of registration **You may NOT be eligible if...** - Your cancer has spread to lymph nodes or other organs - You have a very high predicted risk for lymph node involvement (≥35%) 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

OTHERSBRT

stereotactic radiotherapy of the primary prostate


Locations(1)

UZ Leuven

Leuven, Vlaams Brabant, Belgium

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NCT05344235


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