Effect of Androgen Receptor Signaling Inhibitors on 68Ga-PSMA-11 PET/CT Imaging in Patients With Castration-Resistant Prostate Cancer

Metastatic Prostate Carcinoma Clinical Trial

Official title:

Effects of Novel Androgen Receptor Signaling Inhibitors on PSMA PET Signal Intensity in Patients With Castrate-Resistant Prostate Cancer: A Prospective Exploratory Study

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT04279561
• Other study ID #: 19-002024
• Secondary ID: NCI-2020-00239
• Status: Terminated
• Phase: Phase 1
• Start date: April 16, 2020
• Est. completion date: September 15, 2022

Study information

• Verified date: September 2022
• Source: Jonsson Comprehensive Cancer Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This trial studies the effect of androgen receptor signaling inhibitors on 68Ga-PSMA-11 PET/CT imaging in patients with castration-resistant prostate cancer that has spread to other places in the body (metastatic). Diagnostic procedures, such as 68Ga-PSMA-11 PET/CT, may help in learning how well androgen receptor signaling inhibitors work in killing castration-resistant prostate cancer cells and allow doctors to plan better treatment.

Description:

PRIMARY OBJECTIVE:

I. To evaluate short- and long-term prostate specific membrane antigen (PSMA) imaging changes in response to androgen receptor signaling inhibitors (ARSI).

SECONDARY OBJECTIVES:

I. To correlate PSMA imaging changes with prostate specific antigen (PSA) kinetics.

II. To correlate PSMA imaging changes with progression free survival. III. To evaluate the changes in PSMA PET staging (miTNM Prostate Cancer Molecular Imaging Standardized Evaluation [PROMISE] criteria) under ARSI.

OUTLINE:

Patients receive gallium Ga 68-labeled PSMA-11 (68Ga-PSMA-11) intravenously (IV). After 50-100 minutes, patients undergo positron emission tomography (PET)/computed tomography (CT) over 20-50 minutes. Patients undergo 68Ga-PSMA-11 PET/CT at baseline, at 1 week and 3 months after initiation of ARSI, and at time of biochemical progression (within 1 year if applicable).

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 9
• Est. completion date: September 15, 2022
• Est. primary completion date: September 15, 2022
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically proven prostate cancer

• Know metastatic disease on previous imaging, or PSA value ? 1 ng/ml;

• Castration resistant disease with confirmed testosterone level =< 50 ng/ml under prior first-line androgen deprivation therapy (ADT)

• New planned treatment with enzalutamide or abiraterone, darolutamide or apalutamide

• Willingness to undergo ARSI throughout the duration of the study as prescribed by the treating uro-oncologist

• Stated willingness to comply with continuation of ARSI treatment for the duration of the study

• Provision of signed and dated informed consent form

Exclusion Criteria:

• Inability to provide written informed consent

• Known inability to remain still and lie flat for duration of each imaging procedure (about 30 minutes)

• Other concurrent cytotoxic chemotherapy, immunotherapy, radioligand therapy, or investigational therapy

• A baseline superscan pattern on bone scan

• Diagnosed with other malignancies that are expected to alter life expectancy or may interfere with disease assessment. However, patients with a prior history of malignancy that has been adequately treated and who have been disease free for more than 3 years are eligible

Related Conditions & MeSH terms

• Carcinoma
• Castration-Resistant Prostate Carcinoma
• Metastatic Prostate Carcinoma
• Prostatic Neoplasms
• Stage IV Prostate Cancer American Joint Committee on Cancer (AJCC) v8
• Stage IVA Prostate Cancer AJCC v8
• Stage IVB Prostate Cancer AJCC v8

Intervention

Procedure:
• Computed Tomography
Undergo 68Ga-PSMA-11 PET/CT

Drug:
• Gallium Ga 68 Gozetotide
Given IV

Procedure:
• Positron Emission Tomography
Undergo 68Ga-PSMA-11 PET/CT

Locations

Country	Name	City	State
United States	UCLA / Jonsson Comprehensive Cancer Center	Los Angeles	California

Sponsors (1)

Lead Sponsor	Collaborator
Jonsson Comprehensive Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in 68Ga-PSMA-11 lesion and total-body uptake (standardized uptake value [SUV]max and SUVmean) over time in response to androgen receptor signaling inhibitors (ARSI)	Changes are expressed in terms of percentage changes from baseline positron emission tomography (PET) (before ARSI). Will utilize mixed effect regression models to evaluate the change over time in PSMA results.	Baseline, assessed up to 1 year
Secondary	Prostate specific antigen (PSA) kinetics under ARSI	Comparison of 68Ga-PSMA-11 uptake (SUVmax and SUVmean) changes over time to PSA kinetics under ARSI. Will use mixed effects regression models to correlate the PSMA and PSA time trends. These models will include the effect of time and the PSMA by time interaction effect.	Baseline, assessed up to 1 year
Secondary	Biochemical progression free survival (bPFS)	Correlation between 68Ga-PSMA-11 uptake (SUVmax and SUVmean) changes and time of bPFS under ARSI. Will utilize Cox-proportional hazards regression models. PSMA results will be treated as a time dependent covariate in these models.	Up to 1 year
Secondary	Changes in lesion size on cross sectional imaging under ARSI	Correlation between SUVmax from 68Ga-PSMA-11 PET and lesion size on cross sectional imaging under ARSI.	Up to 1 year
Secondary	Changes in staging (PSMA miTNM PROMISE criteria) under ARSI	Will utilize mixed effects regression models to evaluate the change in staging over time.	Up to 1 year
Secondary	Incidence of adverse events	Assessed by Common Terminology Criteria for Adverse Events 4.03.	Up to 1 year