Prostate CancerOBELIX PCaNCT05344235
Observational Study on Extreme Hypofractionation for Localized Prostate Cancer
An observational study of Prostate Cancer and Radiotherapy, run by Universitaire Ziekenhuizen KU Leuven at 1 site in Belgium.
Trial 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 In the last decade, conventionally fractionated RT (1.8-2.0 Gy per fraction to 78-80 Gy) has been replaced by moderately hypofractionated RT (2.3-3.65 Gy per fraction to… Read more about this study
- Who is it for?
- Any age, men only
- Conditions the study is for
- Prostate Cancer, Radiotherapy, SBRT
- What is being tested?
- SBRT
- How many people
- 246 participants
- Where
- 1 siteBelgium
- Study dates
- 25 Apr 2022to Apr 2032
- How long will I take part?
- 5 Years
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- Men only
- No healthy volunteers
- Child, Adult, Older adult
Study population: localized intermediate or high risk prostate cancer (Roach formule < 35%) (cT1-3a/b cN0 M0)
Who may be able to join
- men ≥ 18 years
- histologically confirmed clinically localized adenocarcinoma of the prostate
- intermediate- or high-risk PCa, defined as
- OR at least one of the following criteria:
- clinical stage: cT2a-c, cT3a or cT3b (AJCC 7th edition)
- Gleason Score ≥ 7 (ISUP grade group 2 or higher)
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- OR at least two of the following criteria:
- clinical stage: cT1c (AJCC 7th edition)
- Gleason Score ≥ 7 (ISUP grade group 2 or higher)
- calculated risk for lymph node involvement (Roach formula) <35%.
- no evidence of disease spread beyond the prostate and/or seminal vesicles
- imaging with mpMRI of the prostate and pelvis (compliant with the PIRADS v2.1 guidelines) within 90 days prior to registration, or required to be performed after registration to the trial
- ability to understand, and willingness to sign, the written informed consent
- willingness to comply with scheduled visits, treatment, and other procedures
Who cannot join
- 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
- clinical stage cT4 (invasion of adjacent organ like bladder or rectum, visualized on mpMRI and/or ultrasound and endoscopy) (AJCC 7th edition)
- significant urinary obstruction of other voiding symptoms (IPSS > 18) is allowed, however should be discussed with the principal investigator and left to the discretion of the treating physician
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- high risk of lymph node involvement, as calculated with the Roach formula ≥ 35% (https://www.evidencio.com/models/show/1144) Of note, in case of ambiguity of regional lymph node involvement on CT or MRI findings (when Roach formula is < 35%, and all other eligibility criteria are met), dedicated imaging with PSMA PET-CT or extended pelvic lymph node dissection must be obtained to rule out lymph node involvement
- evidence of distant metastases (based on CT scan, MRI of the pelvis, bone scan within 90 days prior to registration; if the bone scan is suspicious but not unequivocal, dedicated X-ray and/or MRI must be obtained to rule out metastasis)
- contraindications to MRI according to the Radiology Department guidelines (metal implants, noncompatible cardiac device, deep brain stimulators, cochlear implants, metallic foreign body in the eye or aneurysm clips in the brain, severe claustrophobia).
- World Health Organization (WHO) performance score > 2
- patients with severe inflammatory bowel disease rendering radiotherapy impossible (active Crohn's Disease or Ulcerative Colitis), or patients known with ataxia telangiectasia
- implanted hardware or other material that would prohibit appropriate treatment planning or treatment delivery, in the investigator's opinion
- prior or concurrent invasive malignancy (except non-melanomatous skin cancer) or lymphomatous/hematogenous malignancy unless continually disease-free for a minimum of 5 years.
- (carcinoma in situ of the bladder or oral cavity is permissible)
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Belgium1 site, 1 recruiting
- Recruiting
UZ Leuven
Leuven, Vlaams Brabant, 3000
Charlien Berghen, +16347600, charlien.berghen@uzleuven.be
About this study
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
- Prostate Cancer, Radiotherapy, SBRT
- Being tested
- SBRT
- Medical subject headings
- Prostatic Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
SBRTOther
stereotactic radiotherapy of the primary prostate
What is being measured
The primary outcome is the main question the study is designed to answer.
acute toxicity
acute gastrointestinal (GI) and genitourinary (GU) Common Terminology Criteria for Adverse Events version 5.0 (CTCAE 5.0)
Measured: toxicity occurring within 90 days after the first SBRT session
Secondary outcomes (4)
late toxicity
late GI and GU CTCAE v5.0
Measured: 90 days to 5 years after the last radiation treatment
impact on quality if of life
questionnaires EORTC QLQ-C30, EORTC PR25
Measured: until month 60
(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).
Measured: until month 60
Dose-volume parameters
dose to the organs at risk (Gray, unit)
Measured: until month 60
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Apr 2022
- Study start25 Apr 2022
- Primary completionApr 2027 (estimated)
- Study completionApr 2032 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Prostate CancerStudies of the same condition, open and under way.
- More trials run by Universitaire Ziekenhuizen KU LeuvenThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 246 participants (estimated)
- Target duration
- 5 Years
Sponsor and investigators
- Lead sponsor
- Universitaire Ziekenhuizen KU Leuven
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Gert De Meerleer, MD, PhD, Principal investigator, UZ Leuven
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05344235
- Sponsor's protocol ID
- S66399
- Acronym
- OBELIX PCa
- Status last verified
- Mar 2025
- First submitted
- 12 Apr 2022
- Last updated
- 30 Mar 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: no sharing of IPD due to GDPR
Study at a glance
From the registry record, last updated by the sponsor on 30 Mar 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Observational Study on Extreme Hypofractionation for Localized Prostate Cancer
- ClinicalTrials.gov ID
- NCT05344235
- Acronym / sponsor ID
- OBELIX PCa / S66399
- Conditions
- Prostate Cancer, Radiotherapy, SBRT
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 246 participants (estimated)
- Lead sponsor
- Universitaire Ziekenhuizen KU LeuvenUniversity, hospital or other
- Study start
- 25 Apr 2022 (actual)
- Primary completion
- Apr 2027 (estimated)
- Study completion
- Apr 2032 (estimated)
- First posted
- 25 Apr 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 5 Years
Who may qualify
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- localized intermediate or high risk prostate cancer (Roach formule < 35%) (cT1-3a/b cN0 M0)
Key inclusion criteria (14 listed)
- 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)
- Gleason Score ≥ 7 (ISUP grade group 2 or higher)
Key exclusion criteria (14 listed)
- 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
- clinical stage cT4 (invasion of adjacent organ like bladder or rectum, visualized on mpMRI and/or ultrasound and endoscopy) (AJCC 7th edition)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| SBRTstereotactic radiotherapy of the primary prostate | Other | – |
Primary outcome
acute toxicity
Time frame: toxicity occurring within 90 days after the first SBRT session
acute gastrointestinal (GI) and genitourinary (GU) Common Terminology Criteria for Adverse Events version 5.0 (CTCAE 5.0)
4 secondary outcomes
late toxicity
Time frame: 90 days to 5 years after the last radiation treatment
impact on quality if of life
Time frame: until month 60
(Biochemical and Clinical) Relapse-free survival
Time frame: until month 60
Dose-volume parameters
Time frame: until month 60
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Mar 2025.
- Individual participant dataSharing planned: No. no sharing of IPD due to GDPR
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Gert De Meerleer, MD, PhD principal investigator
UZ Leuven
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Prostate Cancer and Radiotherapy, run by Universitaire Ziekenhuizen KU Leuven at 1 site in Belgium.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 14 inclusion and 14 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 30 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Belgium. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Charlien Berghen, MD, PhD (+3216347600, charlien.berghen@uzleuven.be), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
acute toxicity (time frame: toxicity occurring within 90 days after the first SBRT session). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Mar 2025.