Actively Recruiting
Observational Study on Extreme Hypofractionation for Localized Prostate Cancer
Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2025-03-30
246
Participants Needed
1
Research Sites
518 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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 In the last decade, conventionally fractionated RT (1.8-2.0 Gy per fraction to 78-80 Gy) has been replaced by moderately hypofractionated RT (2.3-3.65 Gy per fraction to 56-70 Gy).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.
CONDITIONS
Official Title
Observational Study on Extreme Hypofractionation for Localized Prostate Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male, 18 years or older
- Histologically confirmed clinically localized adenocarcinoma of the prostate
- Intermediate- or high-risk prostate cancer defined by:
- Clinical stage cT2a-c, cT3a, or cT3b (AJCC 7th edition), or
- Gleason Score 7 or higher (ISUP grade group 2 or higher), or
- At least two of the following: clinical stage cT1c, Gleason Score 7 or higher, calculated lymph node involvement risk less than 35% (Roach formula)
- No evidence of cancer spread beyond the prostate or seminal vesicles
- Imaging with multiparametric MRI of the prostate and pelvis within 90 days prior to or after registration
- Ability to understand and willingness to sign written informed consent
- Willingness to comply with scheduled visits, treatment, and procedures
You will not qualify if you...
- Prior pelvic irradiation (external beam radiotherapy or brachytherapy)
- Previous radical prostatectomy, cryosurgery, or high-intensity focused ultrasound for prostate cancer
- Previous or concurrent cytotoxic chemotherapy for prostate cancer
- Neuroendocrine or small cell carcinoma of the prostate
- Clinical stage cT4 with invasion of adjacent organs like bladder or rectum
- Significant urinary obstruction or other voiding symptoms with IPSS greater than 18 unless discussed with principal investigator
- High risk of lymph node involvement (Roach formula 35% or higher)
- Evidence of distant metastases based on imaging within 90 days prior to registration
- Contraindications to MRI such as certain metal implants or severe claustrophobia
- WHO performance score greater than 2
- Severe inflammatory bowel disease or ataxia telangiectasia
- Implanted hardware preventing appropriate treatment planning or delivery
- Prior or concurrent invasive malignancy (except non-melanomatous skin cancer) or lymphomatous/hematogenous malignancy unless disease-free for at least 5 years (carcinoma in situ of bladder or oral cavity allowed)
AI-Screening
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Trial Site Locations
Total: 1 location
1
UZ Leuven
Leuven, Vlaams Brabant, Belgium, 3000
Actively Recruiting
Research Team
C
Charlien Berghen, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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