Actively Recruiting

Phase 3
Age: 18Years - 80Years
MALE
NCT04642027

PSMA-PET Guided Hypofractionated Salvage Prostate Bed Radiotherapy

Led by University Medical Center Groningen · Updated on 2024-02-28

538

Participants Needed

13

Research Sites

521 weeks

Total Duration

On this page

Sponsors

U

University Medical Center Groningen

Lead Sponsor

D

Dutch Cancer Society

Collaborating Sponsor

AI-Summary

What this Trial Is About

After radical prostatectomy approximately 15-40% of men develop a biochemical recurrence (BR) within 5 years. The standard treatment of post-prostatectomy BR is salvage external beam radiation therapy (sEBRT). sEBRT can provide long-term disease control; with 5 year biochemical progression-free survival (bPFS) up to 60% and with most treatment failures in the first 2 years after sEBRT. The main goal of this project is to investigate whether the oncologic outcome in patients with post-prostatectomy recurrent PCa can be improved, by increasing the biological effective radiation dose using a hypofractionated schedule of 20 x 3 = 60 Gy. The study is designed as a prospective open phase III randomized multicenter trial. All patients with biochemical recurrence with a PSA \< 1.0 ng/ml after radical prostatectomy for prostate cancer without evidence of lymph nodes or distance metastases will be included. PSA progression after prostatectomy defined as two consecutive rises with the final PSA \> 0.1 ng/mL or three consecutive rises will be included. All eligible patients will be randomized to one of the following two treatment arms: Arm 1 = Conventional sEBRT to apply a total dose of 70 Gy in 35 daily fractions of 2 Gy during 7 weeks. Arm 2 = Hypofractionated sEBRT to apply a total dose of 60 Gy in 20 fractions of 3 Gy during 4 weeks. The primary endpoint will be the 5-year progression-free survival (PFS) after treatment.

CONDITIONS

Official Title

PSMA-PET Guided Hypofractionated Salvage Prostate Bed Radiotherapy

Who Can Participate

Age: 18Years - 80Years
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with prostate adenocarcinoma treated with radical prostatectomy
  • Tumour stage pT2-4, R0-1, pN0, or cN0, cNx according to the UICC TNM 2009, with Gleason score available
  • No lymph node or distant metastases shown by a PSMA-PET scan within 60 days before inclusion
  • PSA progression after prostatectomy defined as two consecutive rises with the final PSA > 0.1 ng/mL or three consecutive rises, with the first value measured at least 6 weeks after surgery
  • PSA at inclusion less than 1.0 ng/mL
  • WHO performance status between 0 and 2 at inclusion
  • Age between 18 and 80 years at inclusion
  • Signed and dated informed consent prior to registration
Not Eligible

You will not qualify if you...

  • Prior pelvic irradiation, (chemo)hormonal therapy, or orchiectomy
  • Previous or current active invasive cancers other than superficial non-melanoma skin cancers
  • Positive nodes or distant metastases found by surgical specimen or PSMA-PET/CT scan within 60 days prior to registration
  • Presence of double-sided metallic hip prosthesis
  • Inability or unwillingness to understand trial information, give informed consent, or complete quality of life questionnaires

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 13 locations

1

Radiotherapiegroep

Arnhem, Gelderland, Netherlands

Actively Recruiting

2

Radboud University Medical Center

Nijmegen, Gelderland, Netherlands

Actively Recruiting

3

Maastro Clinic

Maastricht, Limburg, Netherlands

Actively Recruiting

4

Catharina-Hospital

Eindhoven, North Brabant, Netherlands

Actively Recruiting

5

Verbeeten Institute

Tilburg, North Brabant, Netherlands

Actively Recruiting

6

Amsterdam UMC (Location VUmc)

Amsterdam, North Holland, Netherlands

Not Yet Recruiting

7

Radiotherapiegroep

Deventer, Overijssel, Netherlands

Actively Recruiting

8

Radiotherapy Institute Friesland

Leeuwarden, Provincie Friesland, Netherlands

Actively Recruiting

9

Leiden University Medical Center

Leiden, South Holland, Netherlands

Not Yet Recruiting

10

Erasmus Medical Center

Rotterdam, South Holland, Netherlands

Not Yet Recruiting

11

Haga Hospital

The Hague, South Holland, Netherlands

Not Yet Recruiting

12

Zuidwest Radiotherapeutisch Instituut (ZRTI)

Flushing, Netherlands

Actively Recruiting

13

UMCG

Groningen, Netherlands, 9713GZ

Actively Recruiting

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Research Team

F

F. Staal, MD

CONTACT

P

P. Veldhuijzen van Zanten

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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