About this trial
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 In the last decade, conventionally fractionated RT (1.8-2.0 Gy per fraction to 78-80 Gy) has been replaced by moderately hypofractionated RT (2.3-3.65 Gy per fraction to 56-70 Gy).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 criteria
This trial does not accept healthy volunteersQualifiers
men ≥ 18 years
histologically confirmed clinically localized adenocarcinoma of the prostate
intermediate- or high-risk PCa, defined as
clinical stage: cT2a-c, cT3a or cT3b (AJCC 7th edition)
Disqualifiers
prior pelvic irradiation (external beam radiotherapy or brachytherapy)
previous radical prostatectomy, cryosurgery, or HIFU for prostate cancer
previous or concurrent cytotoxic chemotherapy for prostate cancer
patients with neuroendocrine or small cell carcinoma of the prostate
Trial population
localized intermediate or high risk prostate cancer (Roach formule \< 35%) (cT1-3a/b cN0 M0)
Trial design
Cohort
Prospective
Treatments tested in this trial
SBRT
Other interventionstereotactic radiotherapy of the primary prostate
Treatment groups
Trial outcomes
Primary outcomes
acute toxicity
acute gastrointestinal (GI) and genitourinary (GU) Common Terminology Criteria for Adverse Events version 5.0 (CTCAE 5.0)
Secondary outcomes
late toxicity
late GI and GU CTCAE v5.0
impact on quality if of life
questionnaires EORTC QLQ-C30, EORTC PR25
(Biochemical and Clinical) Relapse-free survival
Biochemical disease-free survival will be assessed using the Phoenix consensus definition (time frame = 5 years). Clinical relapse-free survival will be defined by the occurrence of any clinical relapse (local, nodal or distant) captured on state-of-the-art imaging (PSMA PET-CT) and triggered by biochemical recurrence and/or occurrence of disease-related symptoms, or in case of accidental findings on imaging performed for other indications (Kaplan Meier statistics).
Dose-volume parameters
dose to the organs at risk (Gray, unit)
Sponsors and contacts
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