Overview

Long-term Better Than Short-term ADT With Salvage RT

Status:
Not yet recruiting
Trial end date:
2029-02-01
Target enrollment:
0
Participant gender:
Male
Summary
A randomized, multicenter, prospective PHASE II trial to assess the effect of short- versus long-term adjuvant ADT with high dose salvage radiotherapy on distant metastasis free survival in case of biochemical relapse (BR) after radical prostatectomy.
Phase:
Phase 2/Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Universitaire Ziekenhuizen Leuven
Collaborator:
Ipsen
Treatments:
Triptorelin Pamoate
Criteria
Inclusion Criteria:

- History of histologically proven prostate cancer, treated with RP and ePLND. All
patients have to be pN0. The minimal template for ePLND is defined as the removal of
the external iliac, internal iliac and obturator nodes (standard template). Removal of
the presacral and common iliac nodes is left at the discretion of the treating
urologist.

- Asymptomatic PSA-rise post-RP, defined as a value equal to or more than 0.2µg/l and at
least confirmed once (interval ≥2 weeks, confirmation PSA level should be higher). In
case of Gleason 8-10, pT3b or R1 resection, an asymptomatic PSA-rise post-RP starting
from ≥0.15 µg/l is allowed for inclusion. If the PSA-level is less than 0.4 ng/ml, no
additional staging for distant metastasis is required before inclusion in the trial.
The patient will be offered the opportunity to participate in a diagnostic sub-study
with investigational imaging with 18F PSMA PET CT. However in case of PSA-level >0.4
ng/ml, biological imaging using 18F-PSMA or 68Ga-PSMA is mandatory as this is not
considered investigational anymore. Therefore the patient cannot anymore take part in
the diagnostic sub-study and (un-blinded) PET-CT is obligatory to rule out lymph node
(N) and /or distant metastasis (M1a-c) before inclusion.

- Testosterone levels within above 150 ng/dl.

- ECOG 0-1

- Life expectancy more than 5 years

- Signed informed consent

Exclusion Criteria:

- Presence of pN1 disease at original surgical specimen.

- Presence of distant metastasis at time of referral (M1a-c). If PSA more than 0.4
ng/ml, imaging with PET-CT is required to rule out distant metastasis (see above).
Other additional imaging modalities (CT scan, bone scintigraphy...) are allowed but
left at the discretion of the treating centre.

- Undetectable PSA (less than 0.2 ng/ml) at time of referral.

- Previous RT making new RT impossible (overlapping treatment fields).

- Known contraindications to irradiation (Ulcerative Colitis, Crohn Disease, Ataxia
Teleangiectasia…)

- Active treatment with ADT or PSA modulating drugs (finasteride, dutasteride, high-dose
corticoids…)

- Not able understanding treatment protocol or signing informed consent.