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Comparing "Salvage" Radiotherapy and Individualized PSMA PET/CT Targeted Treatment in With Relapsing Prostate Cancer

Primary Purpose

Prostate Cancer

Status
Recruiting
Phase
Phase 3
Locations
Sweden
Study Type
Interventional
Intervention
Individualised therapy
Standard salvage therapy
Sponsored by
Stefan Carlsson
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

Eligibility Criteria

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

Inclusion Criteria:

  • Patients previously treated for prostate cancer with radical prostatectomy and now having a biochemical recurrence (BCR) defined as: PSA >0.2 <2.0 ng/mL, and increasing measured twice.
  • Multidisciplinary conference (MDK) decision to offer the patient SRT
  • Signed Informed Consent

Exclusion Criteria:

  • Patients previously treated for prostate cancer with biochemical recurrence
  • Previous treatment with androgen deprivation therapy (ADT) after surgery
  • Previous pelvic radiotherapy
  • Patients with positive lymph nodes at surgery

Sites / Locations

  • Sahlgrenska University HospitalRecruiting
  • Södersjukhuset
  • Karolinska University HospitalRecruiting
  • Norrland's University Hospital
  • Örebro University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Experimental arm

Control arm

Arm Description

Individualised therapy based on results of the PSMA PET/CT.

Standard salvage therapy. Results of PSMA PET/CT blinded.

Outcomes

Primary Outcome Measures

Primary PSA progression free survival
Number of patients with progress defined by Prostate-Specific Antigen (PSA) measurement

Secondary Outcome Measures

Time to metastasis
Time to documented metastasis of prostate cancer
Prostate cancer specific survival
Time to prostate cancer specific death
Time to secondary treatment
Time to need for secondary treatment for prostate cancer
Differences in quality of life recorded using Patient Reported Outcome Measure (PROM)
A modified version of the PSMA questionnaire developed by the National Prostate Cancer Register. Scale from 1 to 5 were 1 is very good and 5 is very bad.

Full Information

First Posted
March 9, 2021
Last Updated
October 23, 2023
Sponsor
Stefan Carlsson
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1. Study Identification

Unique Protocol Identification Number
NCT04794777
Brief Title
Comparing "Salvage" Radiotherapy and Individualized PSMA PET/CT Targeted Treatment in With Relapsing Prostate Cancer
Official Title
A Randomized Trial Comparing Conventional "Salvage" Radiotherapy and Individualized 68Ga-PSMA-11 or 18F-PSMA-1007 PET/CT Targeted Treatment in Patients With Biochemical Recurrence After Prostate Cancer Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 30, 2018 (Actual)
Primary Completion Date
October 30, 2027 (Anticipated)
Study Completion Date
October 30, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Stefan Carlsson

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
Less than 50% of patients receiving salvage radiation therapy (SRT) to the pelvis as treatment for prostate cancer relapsing after surgery will achieve undetectable Prostate Specific Antigen (PSA) levels. Despite SRT, two-thirds of patients will again develop elevated PSA, 20% will have distant metastases, and 10% will die from prostate cancer within 10 years. The reason for this is probably preexisting distant metastasis and lymph node metastasises which need to better targeted directly. Additionally , there are well known permanent side effects to SRT. Standard imaging techniques have poor sensitivity detecting recurrence when PSA is below 1.0 ng/ml. The surface protein Prostate-specific membrane antigen (PSMA) is overexpressed on prostate cancer cells and 68Gallium (68Ga)- and 18Fluorine (18F)-targeted radioligands have been developed. PSMA PET/CT is used increasingly but there is limited data of its impact. In this study patients with biochemical relapse of prostate cancer after surgery are randomised to the control or experimental group (1:2) and undergo a PSMA PET/CT scan. The experimental group receives individualised therapy based on the result of the PET/CT. The control group receives standard salvage therapy and the result of the PET/CT is blinded. The patients are followed-up with PSA test and quality of life questionnaires.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
PSMA PET/CT

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
450 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental arm
Arm Type
Experimental
Arm Description
Individualised therapy based on results of the PSMA PET/CT.
Arm Title
Control arm
Arm Type
Active Comparator
Arm Description
Standard salvage therapy. Results of PSMA PET/CT blinded.
Intervention Type
Combination Product
Intervention Name(s)
Individualised therapy
Intervention Description
Group I - No uptake: treated with conventional SRT against the prostate bed. Group II -Uptake only in the prostate bed: will receive intensity modulated RT (IMRT) including Volumetric Modulated Arc Therapy (VMAT) for prostate bed with simultaneous-integrated boost (SIB) to the PET positive uptake in the prostate bed. Group III - Uptake in the prostate bed and involvement of regional lymph nodes in the pelvis: will be treated as Group II plus VMAT for the pelvic lymph nodes with SIB to the PET positive lymph nodes or pelvic lymph nodes salvage lymph node dissection (SLND). Group IV - Uptake in regional lymph nodes only: will be treated with VMAT for the pelvic lymph nodes with SIB to the PET positive lymph nodes or pelvic lymph nodes SLND. Group V - Uptake in extra-pelvic lymph nodes or bone metastasis: systemic treatment instead of surgery or radiation. Local treatment with surgery or radiation is acceptable if curative intention.
Intervention Type
Radiation
Intervention Name(s)
Standard salvage therapy
Intervention Description
Standard salvage radiotherapy
Primary Outcome Measure Information:
Title
Primary PSA progression free survival
Description
Number of patients with progress defined by Prostate-Specific Antigen (PSA) measurement
Time Frame
Throughout the study, approximately 10 years.
Secondary Outcome Measure Information:
Title
Time to metastasis
Description
Time to documented metastasis of prostate cancer
Time Frame
At 5, 7 and 10 years
Title
Prostate cancer specific survival
Description
Time to prostate cancer specific death
Time Frame
At 5, 7 and 10 years
Title
Time to secondary treatment
Description
Time to need for secondary treatment for prostate cancer
Time Frame
At 5, 7 and 10 years
Title
Differences in quality of life recorded using Patient Reported Outcome Measure (PROM)
Description
A modified version of the PSMA questionnaire developed by the National Prostate Cancer Register. Scale from 1 to 5 were 1 is very good and 5 is very bad.
Time Frame
Baseline, 6, 12, 36 and 60 months after completed treatment.

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients previously treated for prostate cancer with radical prostatectomy and now having a biochemical recurrence (BCR) defined as: PSA >0.2 <2.0 ng/mL, and increasing measured twice. Multidisciplinary conference (MDK) decision to offer the patient SRT Signed Informed Consent Exclusion Criteria: Patients previously treated for prostate cancer with biochemical recurrence Previous treatment with androgen deprivation therapy (ADT) after surgery Previous pelvic radiotherapy Patients with positive lymph nodes at surgery
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stefan Carlsson
Phone
0704871106
Ext
46
Email
stefan.carlsson@ki.se
First Name & Middle Initial & Last Name or Official Title & Degree
Yvonne Larsen
Email
yvonne.larsen@regionstockholm.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stefan Carlsson
Organizational Affiliation
Karolinska University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sahlgrenska University Hospital
City
Göteborg
ZIP/Postal Code
413 45
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ola Bratt
Email
ola.bratt@vgregion.se
First Name & Middle Initial & Last Name & Degree
Jon Kindblom
Email
jon.kindblom@vgregion.se
First Name & Middle Initial & Last Name & Degree
Ola Bratt
First Name & Middle Initial & Last Name & Degree
Jon Kindblom
Facility Name
Södersjukhuset
City
Stockholm
ZIP/Postal Code
118 83
Country
Sweden
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chunde Li
Email
Chunde.Li@ki.se
First Name & Middle Initial & Last Name & Degree
Gunilla Sellerstam
Email
gunilla.sellerstam@sll.se
First Name & Middle Initial & Last Name & Degree
Chunde Li
Facility Name
Karolinska University Hospital
City
Stockholm
ZIP/Postal Code
171 76
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stefan Carlsson
Email
stefan.carlsson@ki.se
First Name & Middle Initial & Last Name & Degree
Katarina Hammarlund
Email
katarina.hammarlund@sll.se
First Name & Middle Initial & Last Name & Degree
Stefan Carlsson
Facility Name
Norrland's University Hospital
City
Umeå
ZIP/Postal Code
901 85
Country
Sweden
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karin Söderkvist, MD
Email
karin.soderkvist@umu.se
First Name & Middle Initial & Last Name & Degree
Camilla Thellenberg
Email
camilla.thellenberg@umu.se
First Name & Middle Initial & Last Name & Degree
Karin Söderkvist, MD
Facility Name
Örebro University Hospital
City
Örebro
ZIP/Postal Code
701 85
Country
Sweden
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Janusz Frey, MD PhD
Email
janusz.frey@regionorebrolan.se
First Name & Middle Initial & Last Name & Degree
Anna Messing-Eriksson
Email
anna.messing-eriksson@regionorebrolan.se
First Name & Middle Initial & Last Name & Degree
Janusz Frey, MD PhD

12. IPD Sharing Statement

Learn more about this trial

Comparing "Salvage" Radiotherapy and Individualized PSMA PET/CT Targeted Treatment in With Relapsing Prostate Cancer

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