Salvage Stereotactic Body Radiotherapy of the Prostate Bed for Biochemical Recurrence After Radical Prostatectomy.

Last updated: March 28, 2025
Sponsor: Jules Bordet Institute
Overall Status: Active - Recruiting

Phase

N/A

Condition

Prostate Cancer

Treatment

SOC RT

Stereotactic body radiotherapy (SBRT)

stereotactic body radiotherapy

Clinical Study ID

NCT06523634
CE3764
  • Ages > 18
  • Male

Study Summary

This is a a randomized phase II/III trial comparing salvage SBRT with standard of care (SOC) regimens for patients with a persistent detectable PSA or biochemical progression during follow-up after radical prostatectomy.

Eligibility Criteria

Inclusion

INCLUSION CRITERIA

  1. Localized adenocarcinoma (cN0M0) of the prostate treated primarily with radical prostatectomy with definitive intent.

  2. Either persistent PSA after prostatectomy (PSA ≥ 0.1 ng/mL at least 6 weeks after prostatectomy), or biochemical progression (two consecutive rising PSA amounts with a PSA >0.1 ng/mL , or three consecutive PSA rises)

  3. WHO PS 0-1

  4. Age ≥18 years

  5. Ability to understand and willingness to sign a study-specific informed consent prior to study entry

  6. Ability to understand and answer the EPIC-26 form in one of the languages available

EXCLUSION CRITERIA

  1. Patients with a pT4 tumor at prostatectomy

  2. Patients with previously pathologically confirmed N1

  3. Patients with macroscopically involved margin at surgery (R2)

  4. Patients with a history of distant metastases

  5. Patients with a recurrence visible on imaging (local, pelvic, or distant). Pelvic nodes with a small diameter >1cm and/or positive on PSMA without other explanation, are considered as a pelvic recurrence.

  6. Latest PSA > 2ng/ml

  7. Patients with a IPSS >20

  8. Gleason 10 tumor

  9. Prior history of high-intensity focused ultrasound ablation (HIFU), cryosurgery or brachytherapy of the prostate

  10. Prior pelvic radiotherapy

  11. Prior hormonal therapy started more than 6 weeks before randomization

  12. History of inflammatory bowel disease, ataxia telangiectasia, prior rectal or bladder surgery.

  13. Other active malignancy, except non-melanoma skin cancer, superficial bladder cancer, or malignancies with a documented disease-free survival for a minimum of 3 years before randomization.

Study Design

Total Participants: 284
Treatment Group(s): 3
Primary Treatment: SOC RT
Phase:
Study Start date:
December 10, 2024
Estimated Completion Date:
February 01, 2032

Study Description

This is a multicentric randomized seamless phase II/III study comparing SBRT to conventional RT or moderately hypofractionated RT on the prostate bed.

All subjects will be randomly assigned in a 1:1 ratio:

  1. Experimental arm: Radiotherapy treatment in 5 fractions.

  2. Control arm: Radiotherapy treatment within a normofractionated or mildly hypofractionated schedule. For the control arm, each participating center can choose between a normofractionated schedule (32 to 35 treatment sessions) and a moderately hypofractionated schedule (20 sessions).

Connect with a study center

  • AZorg

    Aalst,
    Belgium

    Site Not Available

  • Ziekenhuis Aan de Stroom (ZAS)

    Antwerpen,
    Belgium

    Active - Recruiting

  • Jules Bordet Institute, H.U.B

    Brussels,
    Belgium

    Active - Recruiting

  • Jessa Ziekenhuis

    Hasselt,
    Belgium

    Site Not Available

  • CHU HELORA - Hôpital de La Louvière - site Jolimont

    La Louvière,
    Belgium

    Site Not Available

  • AZ Sint-Maarten

    Mechelen,
    Belgium

    Site Not Available

  • CHU UCL Namur - Site Elisabeth

    Namur,
    Belgium

    Active - Recruiting

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