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PSMA-PET Guided Hypofractionated Salvage Prostate Bed Radiotherapy (PERYTON)

Primary Purpose

Prostate Cancer, Cancer Recurrence

Status
Recruiting
Phase
Phase 3
Locations
Netherlands
Study Type
Interventional
Intervention
Conventional sEBRT
Hypofractionated sEBRT
Sponsored by
University Medical Center Groningen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring PSMA-PET/CT, Salvage, Hypofractionation, Radiotherapy, Prostatectomy

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with prostate adenocarcinoma treated with radical prostatectomy;
  • Tumour stage pT2-4, R0-1, pN0, or cN0, cNx according to the UICC TNM 2009, only with Gleason score available;
  • No lymph node or distant metastases. A recent PSMA-PET scan (< 60 days) without evidence of lymph node or distant metastases;
  • PSA progression after prostatectomy defined as two consecutive rises with the final PSA > 0.1 ng/mL or 3 consecutive rises. The first value must be measured at least 6 weeks after radical prostatectomy;
  • PSA at inclusion < 1.0 ng/mL;
  • WHO performance status 0-2 at inclusion;
  • Age at inclusion between 18 and 80 years;
  • Written (signed and dated) informed consent prior to registration.

Exclusion Criteria:

  • Prior pelvic irradiation, (chemo)hormonal therapy or orchiectomy;
  • Previous or concurrent active invasive cancers other than superficial non-melanoma skin cancers;
  • Patients with positive nodes or with distant metastases based on the surgical specimen of lymphadenectomy or the following minimum diagnostic workup: PSMA-PET/CT scan, 60 days prior to registration;
  • Double-sided metallic hip prosthesis;
  • Inability or unwillingness to understand the information on trial-related topics, to give informed consent or to fill out QoL questionnaires.

Sites / Locations

  • Radiotherapy Institute FrieslandRecruiting
  • RadiotherapiegroepRecruiting
  • Radboud University Medical CenterRecruiting
  • Maastro ClinicRecruiting
  • Catharina-Hospital
  • Verbeeten InstituteRecruiting
  • Amsterdam UMC (Location VUmc)
  • RadiotherapiegroepRecruiting
  • Haga Hospital
  • Leiden University Medical Center
  • Erasmus Medical Center
  • UMCGRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Conventional

Hypofractionation

Arm Description

Conventional sEBRT

Hypofractionated sEBRT

Outcomes

Primary Outcome Measures

5-year progression-free survival
Defined as biochemical progression, clinical progression, loco-regional or distant progression or start with hormonal therapy, whichever occurs first

Secondary Outcome Measures

Acute grade ≥ 2 gastrointestinal toxicity
As assessed using physician-reported score: Common Terminology Criteria for adverse events version 5.0 (CTCAE-5) toxicity score with a scale of 1 - 4.
Acute grade ≥ 2 genitourinary toxicities
As assessed using physician-reported score using questionnaires (CTCAE 5.0 toxicity score).
Late grade ≥ 2 gastrointestinal toxicity
As assessed using physician-reported score (CTCAE 5.0 toxicity score).
Late grade ≥ 2 genitourinary toxicity
Using physician-reported score (CTCAE 5.0 toxicity score).
Quality of life after radiation
As assessed using patient-reported questionnaires: measurend with European platform of cancer research-QLQ C30
Metastasis-free survival
Time from randomisation to the date of metastases reported by CT scan, MRI scan or PSMA-PET/CT during the follow up (date scan).
Prostate cancer-specific mortality
Prostate cancer-specific mortality.
Overall survival
Overall survival
Acute grade ≥ 2 gastrointestinal toxicity
Using patient-reported questionnaires (Radiation Therapy Oncology Group (RTOG) / European platform of cancer research (EORTC) toxicity questionnaires with grade 1 to 4).
Acute grade ≥ 2 genitourinary toxicities
Using patient-reported questionnaires (Radiation Therapy Oncology Group (RTOG) / European platform of cancer research (EORTC) toxicity questionnaires with grade 1 to 4).
Late grade ≥ 2 genitourinary toxicity
Using patient-reported questionnaires (Radiation Therapy Oncology Group (RTOG) / European platform of cancer research (EORTC) toxicity questionnaires with grade 1 to 4).
Quality of life after radiation
As assessed using patient reported quatinnaires: European platform of cancer research-Quality of Life Questionnaire - Prostate Cancer Module (PR 25).

Full Information

First Posted
August 13, 2020
Last Updated
April 5, 2022
Sponsor
University Medical Center Groningen
Collaborators
Dutch Cancer Society
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1. Study Identification

Unique Protocol Identification Number
NCT04642027
Brief Title
PSMA-PET Guided Hypofractionated Salvage Prostate Bed Radiotherapy
Acronym
PERYTON
Official Title
PSMA-PET Guided Hypofractionated Salvage Prostate Bed Radiotherapy of Biochemical Failure After Radical Prostatectomy for Prostate Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2020 (Actual)
Primary Completion Date
September 1, 2029 (Anticipated)
Study Completion Date
September 1, 2030 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Medical Center Groningen
Collaborators
Dutch Cancer Society

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer, Cancer Recurrence
Keywords
PSMA-PET/CT, Salvage, Hypofractionation, Radiotherapy, Prostatectomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
2 randomised arms
Masking
None (Open Label)
Masking Description
no masking
Allocation
Randomized
Enrollment
538 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Conventional
Arm Type
Active Comparator
Arm Description
Conventional sEBRT
Arm Title
Hypofractionation
Arm Type
Experimental
Arm Description
Hypofractionated sEBRT
Intervention Type
Radiation
Intervention Name(s)
Conventional sEBRT
Other Intervention Name(s)
Conventional salvage external beam radiation therapy
Intervention Description
A total dose of70 Gy in 35 daily fractions of 2 Gy during 7 weeks
Intervention Type
Radiation
Intervention Name(s)
Hypofractionated sEBRT
Other Intervention Name(s)
Hypofractionated salvage external beam radiation therapy
Intervention Description
A total dose of 60 Gy in 20 daily fractions of 3 Gy during 4 weeks
Primary Outcome Measure Information:
Title
5-year progression-free survival
Description
Defined as biochemical progression, clinical progression, loco-regional or distant progression or start with hormonal therapy, whichever occurs first
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Acute grade ≥ 2 gastrointestinal toxicity
Description
As assessed using physician-reported score: Common Terminology Criteria for adverse events version 5.0 (CTCAE-5) toxicity score with a scale of 1 - 4.
Time Frame
Up to 3 months after completion of the RT
Title
Acute grade ≥ 2 genitourinary toxicities
Description
As assessed using physician-reported score using questionnaires (CTCAE 5.0 toxicity score).
Time Frame
Up to 3 months after completion of the RT
Title
Late grade ≥ 2 gastrointestinal toxicity
Description
As assessed using physician-reported score (CTCAE 5.0 toxicity score).
Time Frame
Up to 5 years after completion of the RT
Title
Late grade ≥ 2 genitourinary toxicity
Description
Using physician-reported score (CTCAE 5.0 toxicity score).
Time Frame
Up to 5 years after completion of the RT
Title
Quality of life after radiation
Description
As assessed using patient-reported questionnaires: measurend with European platform of cancer research-QLQ C30
Time Frame
Up to 5 years after completion of the RT
Title
Metastasis-free survival
Description
Time from randomisation to the date of metastases reported by CT scan, MRI scan or PSMA-PET/CT during the follow up (date scan).
Time Frame
5 years
Title
Prostate cancer-specific mortality
Description
Prostate cancer-specific mortality.
Time Frame
5 years
Title
Overall survival
Description
Overall survival
Time Frame
5 years
Title
Acute grade ≥ 2 gastrointestinal toxicity
Description
Using patient-reported questionnaires (Radiation Therapy Oncology Group (RTOG) / European platform of cancer research (EORTC) toxicity questionnaires with grade 1 to 4).
Time Frame
Up to 3 months after completion of the RT
Title
Acute grade ≥ 2 genitourinary toxicities
Description
Using patient-reported questionnaires (Radiation Therapy Oncology Group (RTOG) / European platform of cancer research (EORTC) toxicity questionnaires with grade 1 to 4).
Time Frame
Up to 3 months after completion of the RT
Title
Late grade ≥ 2 genitourinary toxicity
Description
Using patient-reported questionnaires (Radiation Therapy Oncology Group (RTOG) / European platform of cancer research (EORTC) toxicity questionnaires with grade 1 to 4).
Time Frame
Up to 5 years after completion of the RT
Title
Quality of life after radiation
Description
As assessed using patient reported quatinnaires: European platform of cancer research-Quality of Life Questionnaire - Prostate Cancer Module (PR 25).
Time Frame
Up to 5 years after completion of the RT

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with prostate adenocarcinoma treated with radical prostatectomy; Tumour stage pT2-4, R0-1, pN0, or cN0, cNx according to the UICC TNM 2009, only with Gleason score available; No lymph node or distant metastases. A recent PSMA-PET scan (< 60 days) without evidence of lymph node or distant metastases; PSA progression after prostatectomy defined as two consecutive rises with the final PSA > 0.1 ng/mL or 3 consecutive rises. The first value must be measured at least 6 weeks after radical prostatectomy; PSA at inclusion < 1.0 ng/mL; WHO performance status 0-2 at inclusion; Age at inclusion between 18 and 80 years; Written (signed and dated) informed consent prior to registration. Exclusion Criteria: Prior pelvic irradiation, (chemo)hormonal therapy or orchiectomy; Previous or concurrent active invasive cancers other than superficial non-melanoma skin cancers; Patients with positive nodes or with distant metastases based on the surgical specimen of lymphadenectomy or the following minimum diagnostic workup: PSMA-PET/CT scan, 60 days prior to registration; Double-sided metallic hip prosthesis; Inability or unwillingness to understand the information on trial-related topics, to give informed consent or to fill out QoL questionnaires.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
F. Staal, MD
Phone
0031655257985
Email
f.h.e.staal@umcg.nl
First Name & Middle Initial & Last Name or Official Title & Degree
P. Veldhuijzen van Zanten
Phone
0031503614659
Email
peryton@rt.umcg.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
S. Aluwini, Dr.
Organizational Affiliation
UMCG
Official's Role
Principal Investigator
Facility Information:
Facility Name
Radiotherapy Institute Friesland
City
Leeuwarden
State/Province
Friesland
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
M. De Jong, MD
Facility Name
Radiotherapiegroep
City
Arnhem
State/Province
Gelderland
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
D. Haverkort, MD
Facility Name
Radboud University Medical Center
City
Nijmegen
State/Province
Gelderland
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
R.J. Smeenk, MD, PhD
Facility Name
Maastro Clinic
City
Maastricht
State/Province
Limburg
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
B. Vanneste, MD
Facility Name
Catharina-Hospital
City
Eindhoven
State/Province
Noord Brabant
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
T.C.G. Budiharto, MD, PhD
Facility Name
Verbeeten Institute
City
Tilburg
State/Province
Noord-Brabant
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
M.A.E. van de Sande, MD
Facility Name
Amsterdam UMC (Location VUmc)
City
Amsterdam
State/Province
Noord-Holland
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
J. van Moorselaar, Professor
Facility Name
Radiotherapiegroep
City
Deventer
State/Province
Overijssel
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
D. Haverkort, MD
Facility Name
Haga Hospital
City
Den Haag
State/Province
Zuid-Holland
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
B. Hollman, MD
Facility Name
Leiden University Medical Center
City
Leiden
State/Province
Zuid-Holland
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
S. Rademakers, MD, PhD
Facility Name
Erasmus Medical Center
City
Rotterdam
State/Province
Zuid-Holland
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
L. Incocci, Professor
Facility Name
UMCG
City
Groningen
ZIP/Postal Code
9713GZ
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
F.H.E. Staal, MD.
Email
PERYTON@rt.umcg.nl

12. IPD Sharing Statement

Citations:
PubMed Identifier
35428210
Citation
Staal FHE, Janssen J, Brouwer CL, Langendijk JA, Ng Wei Siang K, Schuit E, de Jong IJ, Verzijlbergen JF, Smeenk RJ, Aluwini S. Phase III randomised controlled trial on PSMA PET/CT guided hypofractionated salvage prostate bed radiotherapy of biochemical failure after radical prostatectomy for prostate cancer (PERYTON-trial): study protocol. BMC Cancer. 2022 Apr 15;22(1):416. doi: 10.1186/s12885-022-09493-5.
Results Reference
derived

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PSMA-PET Guided Hypofractionated Salvage Prostate Bed Radiotherapy

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