Early Salvage Therapy for Patients With Advanced Features for Biochemical Relapse After Radical Prostatectomy for Localized Prostate Carcinoma In Correlation With Supposed Molecular-genetic Parameters of Higher Aggressiveness
ESTABLISH
1 other identifier
interventional
380
0 countries
N/A
Brief Summary
The primary objective of the trial is to compare the impact and safety of delayed salvage therapy (dSRT, i.e., SRT initiated at PSA values of 0.4-0.5 ng/ml) to those of early salvage therapy (eSRT, i.e., at PSA levels of 0.2 ng/ml) in patients with biochemical relapse after radical prostatectomy. The secondary objective of the trial is to perform analysis of the subgroups of patients to determine which patients are most likely to benefit from dSRT Exploratory objective of the trial is to determine whether selected molecular genetic parameters (172 candidate genes and molecular alterations) and known clinical parameters can be used to identify potential predictors of worse prognosis in patients with known risk factors for relapse after radical prostatectomy, thereby augmenting and refining patient stratification, optimizing their therapy, and clarifying the proper timing of multimodal therapy
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_3 prostate-cancer
Started Sep 2022
Longer than P75 for phase_3 prostate-cancer
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 24, 2021
CompletedFirst Posted
Study publicly available on registry
February 10, 2022
CompletedStudy Start
First participant enrolled
September 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2032
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2032
August 3, 2022
August 1, 2022
10.3 years
November 24, 2021
August 2, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Event-free survival (EFS)
Defined as a time to re-documented biochemical relapse after salvage therapy (bRFS), demonstration of clinical relapse (i.e.,local relapse /lRFS/, locoregional relapse /lrRFS/, distant relapse /MFS/) and/or death from any cause.
Analysed 3 years after randomisation of the last patient.
Secondary Outcomes (4)
Carcinoma-specific survival (CSS)
Analysed 5/10 years after randomization of the last patient.
Overall survival (5y- and 10y- OS)
Analysed 5/10 years after randomization of the last patient.
Incidence of treatment-related acute and late toxicity
Analysed 5 years after randomization of the last patient.
Health-related quality of life (QoL) assessment.
Analysed 5 years after randomization of the last patient.
Study Arms (2)
Arm A- early salvage radiotherapy (eSRT)
EXPERIMENTALEarly salvage radiotherapy (eSRT) will be administered immediately after the confirmation of the biochemical relapse (prostate-specific antigen PSA level increase to ≈ 0,2 ng/ml) after radical prostatectomy with defined risk factors and no clinical recurrence signs on prostate specific membrane antigen positron emission tomography and computed tomography (PSMA PET/CT).
Arm B- delayed salvage radiotherapy (dSRT)
EXPERIMENTALThe patient is by the biochemical relapse analysis (PSA level 0,2 ng/ml) referred for further follow-up of PSA values. dSRT is initiated, if PSA further increase to values of ≥ 0.4 ng/ml is confirmed and the presence of a potential clinical relapse is excluded with repeated PSMA-PET-CT in line with standard procedures
Interventions
eSRT administered immediately after the confirmation of the biochemical relapse (PSA ≈ 0.2ng/ml). 66-70Gy will be delivered to the bed of prostate. Radiotherapy will be optionally accompanied by androgen deprivation therapy.
dSRT administered if PSA levels increase to ≥ 0.4 ng/ml. 66-70Gy will be delivered to the bed of prostate. Radiotherapy will be optionally accompanied by androgen deprivation therapy.
Eligibility Criteria
You may qualify if:
- \> 18 years of age
- Pathologically confirmed invasive prostate carcinoma with minimal 1 risk factor (RF) after radical prostatectomy (RP)
- Patient refuses the adjuvant therapy after normalization of urinary function within 6 month after RP
- Signed informed consent to participate in the study and (where necessary) consent to participate in the translational part of the research (not a requirement)
- ECOG 0 - 1
- pT2 and minimal 1 risk factor (RF):
- R1 (PSM), and/or
- Gleason score (4+3=7) 8-10 and/or ISUP grade group 3-5
- pT3a /pT3b with or without one RF
- No evidence of suspicious pelvic lymph nodes by initial diagnostic: cN0 and/or pN0
- No evidence of suspicious distant metastases by initial diagnostic: M0
- Patient with decline of PSA level to undetectable PSA levels (\< 0,1 ng/ml) or around 0,2ng/ml and with another decreasing trends so that the PSA level decline within 12-24 weeks after RP to undetectable levels (\< 0,1 ng/ml) and with renewed increase of PSA \>0,2 ng/ml (BCR= biochemical relapse) without any clinical relapse on PSMA PET/CT
- No hormonal therapy prior and /or after the radical prostatectomy
- Patient suitable and fit for subsequent radiotherapy with high likelihood of good compliance to the follow-up
You may not qualify if:
- Life expectancy (based on Charlson comorbidity index) \< 10 years
- Patient not fit for the therapy
- History of other cancer (other than a radically removed non-melanoma skin carcinoma)
- Previous pelvic irradiation
- Active immunosuppressive medication
- History of hormone therapy prior to randomization
- cN1 and/or pN1 and M1
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (27)
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PMID: 33186618BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator, Radiation oncology head
Study Record Dates
First Submitted
November 24, 2021
First Posted
February 10, 2022
Study Start
September 1, 2022
Primary Completion (Estimated)
December 1, 2032
Study Completion (Estimated)
December 1, 2032
Last Updated
August 3, 2022
Record last verified: 2022-08
Data Sharing
- IPD Sharing
- Will not share