Skip to content

The Effect of ADT on PSMA-PET.

The Effect of Androgen Deprivation Therapy on Prostate Specific Membrane Antigen (PSMA) in Prostate Cancer

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03313726
Acronym
ADTPSMA
Enrollment
30
Registered
2017-10-18
Start date
2017-09-20
Completion date
2018-09-30
Last updated
2017-10-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Keywords

PSMA-PET

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.

Interventions

DRUGGnRH antagonist

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.

Sponsors

Turku University Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
40 Years to 85 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
GnRh-antagonist, A0, 7, 14 and 28 days after ADT initiationMaximum SUV in PSMA-PET
GnRh-antagonist, B0 and 7, 14 or 28 days after ADT initiation according to phase ASensitivity and specificity of pre and post ADT 68Ga-PSMA-11 PET/MRI and standard clinical MRI using histology as a reference

Secondary

MeasureTime frameDescription
GnRh-antagonist, A0, 7, 14 and 28 days after ADT initiationTestosterone level (nmol/l)
GnRh-antagonist, B56 and 112 days after ADT initiationTestosterone level (nmol/l)

Countries

Finland

Contacts

Primary ContactJukka Kemppainen, MD, PhD
jukka.kemppainen@tyks.fi+358-2-3130196
Backup ContactOtto Ettala, MD, PhD
otto.ettala@tyks.fi+358-2-3130280

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026