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The Effect of ADT on PSMA-PET. (ADTPSMA)

Primary Purpose

Prostate Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
GnRH antagonist
GnRH antagonist
Sponsored by
Turku University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Prostate Cancer focused on measuring PSMA-PET

Eligibility Criteria

40 Years - 85 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age: 40 to 85 years old
  • Language spoken: Finnish
  • Diagnosis: Histologically confirmed adenocarcinoma of prostate
  • Adequate histological sampling consisting of at least 3 biopsy samples from each lobe
  • No previous surgical, radiation or endocrine treatment for prostate carcinoma
  • Clinical stage: T1c-T4N0-2M0-1 (arm, A); T1c-T3NxMx (arm, B)
  • Serum creatinine ≤ 1,5 x ULN
  • Patient agrees to undergo surgery (arm, B)
  • Mental status: Patients must be able to understand the meaning of the study
  • Informed consent: The patient must sign the appropriate Ethical Committee (EC) approved informed consent documents in the presence of the designated staff

Exclusion Criteria:

  • Infections: Patient must not have an uncontrolled serious infection
  • contraindications for MRI (cardiac pacemaker, intracranial clips etc)
  • Prior usage of 5-ARI medication in past 12 months
  • Patient preference for active surveillance as a method of prostate cancer management

Sites / Locations

  • Turku University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

GnRh-antagonist A

GnRh-antagonist B

Arm Description

Outcomes

Primary Outcome Measures

GnRh-antagonist, A
Maximum SUV in PSMA-PET
GnRh-antagonist, B
Sensitivity and specificity of pre and post ADT 68Ga-PSMA-11 PET/MRI and standard clinical MRI using histology as a reference

Secondary Outcome Measures

GnRh-antagonist, A
Testosterone level (nmol/l)
GnRh-antagonist, A
PSA level (ug/l)
GnRh-antagonist, B
Testosterone level (nmol/l)
GnRh-antagonist, B
EPIC-questionnaire total and hormonal score

Full Information

First Posted
October 9, 2017
Last Updated
October 13, 2017
Sponsor
Turku University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03313726
Brief Title
The Effect of ADT on PSMA-PET.
Acronym
ADTPSMA
Official Title
The Effect of Androgen Deprivation Therapy on Prostate Specific Membrane Antigen (PSMA) in Prostate Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Unknown status
Study Start Date
September 20, 2017 (Actual)
Primary Completion Date
September 30, 2018 (Anticipated)
Study Completion Date
September 30, 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Turku University Hospital

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
Phase A: To describe and to determine the maximum standardised uptake values (SUV) in prostate specific membrane antigen positron emission tomography (PSMA-PET) before ADT and 7, 14 and 28 days after ADT. Phase B: To validate phase A results by comparing the PSMA-PET findings to histopathological analysis of regional lymph nodes acquired from radical prostatectomy specimens. PSMA-PET is done before ADT and at maximum SUV defined by the phase A.
Detailed Description
Positron emission tomography has been commonly and successfully used, in combination with CT and MRI devices, in the staging of intermediate or high risk prostate cancer. Proper staging is essential to guide the treatment options, which usually are radical prostatectomy or radiotherapy in localized prostate cancer or hormonal treatment in patients with metastasized disease, patients with hormonal relapse after radical radiotherapy or as an adjuvant treatment together with radiotherapy. The use of PET imaging increases the sensitivity in the evaluation of lymph node involvement, as almost 80% of metastatic lymph nodes in prostate cancer are smaller than the threshold size usually measured with CT or MRI. Nowadays new specific receptor targeted PET tracers in prostate cancer imaging has been introduced. One of the most used is 68Ga-PSMA that evaluates the expression of prostate-specific membrane antigen. This tracer has been rapidly taken into account for its better sensitivity and specificity in prostate cancer staging compared to the lipid metabolism tracers, like 11C/18F labeled fluorocholine or 11C-acetate. In the recent literature it has been demonstrated for the first time on humans that PSMA expression, imaged with 68Ga-PSMA-11-PET, has increased in a patient with metastatic prostate cancer after androgen deprivation therapy (ADT). These findings suggest that the use of hormonal therapy can affect the expression of PSMA and our hypothesis is that ADT therapy could increase the sensitivity of 68Ga-PSMA PET to detect nodal or distant metastasis in patients with prostate cancer. This prospective study consists in two phases. In phase A, 5 patients with newly diagnosed high risk prostate cancer with PSMA-positive nodal or distant metastasis screened by 68Ga-PSMA-11 PET/MRI, are given androgen deprivation therapy (ADT) with GNRH antagonist. After ADT therapy initiation, 68Ga-PSMA-11 PET/MRI is repeated at 7, 14 and 30 days to determine the highest PSMA expression based on SUVmax measurement. In phase B, 20 high risk prostate cancer patients determined to undergo radical prostatectomy are screened with 68Ga-PSMA-11 PET/MRI, and then given GNRH antagonist therapy. 68Ga-PSMA-11 PET/MRI is repeated at the time of maximum PSMA expression based on phase A results. The patients then undergo radical prostatectomy and lymphadenectomy and imaging findings are matched with histological data.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
GnRh-antagonist A
Arm Type
Experimental
Arm Title
GnRh-antagonist B
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
GnRH antagonist
Intervention Description
Administration of GnRh antagonist after baseline PSMA-PET at day 0 and then repeated PSMA-PET scans at day 7, day 14 and day 28 to define the timeframe of the SUV-max.
Intervention Type
Drug
Intervention Name(s)
GnRH antagonist
Intervention Description
Administration of GnRh-antagonist after baseline PSMA-PET at day 0 and then repeated scan at day in which SUV-max was observed in the Arm A (day 7, day 14 or day 28). Then robot assisted radical prostatectomy and lymphadenectomy are performed to verify the finding.
Primary Outcome Measure Information:
Title
GnRh-antagonist, A
Description
Maximum SUV in PSMA-PET
Time Frame
0, 7, 14 and 28 days after ADT initiation
Title
GnRh-antagonist, B
Description
Sensitivity and specificity of pre and post ADT 68Ga-PSMA-11 PET/MRI and standard clinical MRI using histology as a reference
Time Frame
0 and 7, 14 or 28 days after ADT initiation according to phase A
Secondary Outcome Measure Information:
Title
GnRh-antagonist, A
Description
Testosterone level (nmol/l)
Time Frame
0, 7, 14 and 28 days after ADT initiation
Title
GnRh-antagonist, A
Description
PSA level (ug/l)
Time Frame
0, 7, 14 and 28 days after ADT initiation
Title
GnRh-antagonist, B
Description
Testosterone level (nmol/l)
Time Frame
56 and 112 days after ADT initiation
Title
GnRh-antagonist, B
Description
EPIC-questionnaire total and hormonal score
Time Frame
56 and 112 days after ADT initiation

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 40 to 85 years old Language spoken: Finnish Diagnosis: Histologically confirmed adenocarcinoma of prostate Adequate histological sampling consisting of at least 3 biopsy samples from each lobe No previous surgical, radiation or endocrine treatment for prostate carcinoma Clinical stage: T1c-T4N0-2M0-1 (arm, A); T1c-T3NxMx (arm, B) Serum creatinine ≤ 1,5 x ULN Patient agrees to undergo surgery (arm, B) Mental status: Patients must be able to understand the meaning of the study Informed consent: The patient must sign the appropriate Ethical Committee (EC) approved informed consent documents in the presence of the designated staff Exclusion Criteria: Infections: Patient must not have an uncontrolled serious infection contraindications for MRI (cardiac pacemaker, intracranial clips etc) Prior usage of 5-ARI medication in past 12 months Patient preference for active surveillance as a method of prostate cancer management
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jukka Kemppainen, MD, PhD
Phone
+358-2-3130196
Email
jukka.kemppainen@tyks.fi
First Name & Middle Initial & Last Name or Official Title & Degree
Otto Ettala, MD, PhD
Phone
+358-2-3130280
Email
otto.ettala@tyks.fi
Facility Information:
Facility Name
Turku University Hospital
City
Turku
ZIP/Postal Code
20520
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jukka Kemppainen, MD, PhD
Phone
+358-2-3130196
Email
jukka.kemppainen@tyks.fi
First Name & Middle Initial & Last Name & Degree
Otto Ettala, MD, PhD
Phone
+358-2-3130280
Email
otto.ettala@tyks.fi

12. IPD Sharing Statement

Citations:
PubMed Identifier
31879814
Citation
Ettala O, Malaspina S, Tuokkola T, Luoto P, Loyttyniemi E, Bostrom PJ, Kemppainen J. Prospective study on the effect of short-term androgen deprivation therapy on PSMA uptake evaluated with 68Ga-PSMA-11 PET/MRI in men with treatment-naive prostate cancer. Eur J Nucl Med Mol Imaging. 2020 Mar;47(3):665-673. doi: 10.1007/s00259-019-04635-7. Epub 2019 Dec 26.
Results Reference
derived

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The Effect of ADT on PSMA-PET.

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