Actively Recruiting
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
Eligibility Criteria
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
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
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Complete this quick 3-step screening to check your eligibility
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
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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