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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.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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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 In the last decade, conventionally fractionated RT (1.8-2.0 Gy per fraction to 78-80 Gy) has been replaced by moderately hypofractionated RT (2.3-3.65 Gy per fraction to… Read more about this study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
Show all 14Show fewer
  • 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.

Charlien Berghen, MD, PhD contact

+3216347600

charlien.berghen@uzleuven.be

Belgium1 site, 1 recruiting
  • UZ Leuven

    Leuven, Vlaams Brabant, 3000

    Charlien Berghen, +16347600, charlien.berghen@uzleuven.be

    Recruiting

Other trials in Belgium

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.

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.

  1. 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)
  1. late toxicity

    late GI and GU CTCAE v5.0

    Measured: 90 days to 5 years after the last radiation treatment

  2. impact on quality if of life

    questionnaires EORTC QLQ-C30, EORTC PR25

    Measured: until month 60

  3. (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

  4. 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.

  1. First posted25 Apr 2022
  2. Study start25 Apr 2022
  3. Primary completionApr 2027 (estimated)
  4. Study completionApr 2032 (estimated)

Resources

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
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

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.

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