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Validation of FACBC for Detection of Metastasis Among High-risk Prostate Cancer Patients With Presumed Localized Disease

Validation of FACBC as an Early Indicator of Sub-clinical Metastatic Disease Among High-risk Prostate Cancer Patients With Presumed Localized Disease

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03081884
Acronym
EDRN-FACBC
Enrollment
61
Registered
2017-03-16
Start date
2017-03-01
Completion date
2019-12-31
Last updated
2021-01-25

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

Conditions

Cancer

Keywords

Prostate cancer, Metastatic cancer, Urogenital disorders, Oncology, Radiology

Brief summary

This study is for patients who have a high risk of metastatic prostate cancer (cancer that has spread outside of the prostate) who are going to have radical prostatectomy. The Anti-1-amino-3-\[18F\]fluorocyclobutyl-1-carboxylic acid (FACBC or Fluciclovine) positron emission tomography (PET) scan is a new imaging approach that has promising results in showing progression of cancer. The goal of this study is to determine if FACBC PET imaging will detect metastatic disease in patients with high risk prostate cancer who have negative conventional cross-sectional imaging such as computed tomography (CT) and/or magnetic resonance imaging (MRI), as well as bone scan and/or sodium fluoride PET. FACBC PET imaging may help detect metastatic prostate cancer in patients with newly diagnosed high risk primary prostate cancer and potentially improve staging of the cancer. Additionally, the researchers will compare the FACBC uptake in the prostate with uptake of FACBC detected in metastasis. They will also analyze and compare the prostate tissue, serum and urine parameters that are linked to higher rates of FACBC positivity.

Detailed description

Approximately 50-80% of patients who are considered high-risk after being treated with definitive radical prostatectomy experience recurrent disease, often because of undetected extra-prostatic metastatic disease prior to treatment. There is increasing evidence that performing radical prostatectomy in patients with high-risk disease or locally advanced disease is feasible and has potential benefits in terms of local control, overall survival, and quality of life. Thus, improved imaging approaches for early detection of occult metastatic prostate cancer at the time of presentation could inform a directed treatment approach that would significantly improve patient outcomes, including use of extended lymphadenectomy as well as postoperative radiation therapy planning. Amino acid transport is up-regulated in prostate and other cancers. Anti-1-amino-3-\[18F\]fluorocyclobutyl-1-carboxylic acid (FACBC) is a synthetic amino acid analog positron emission tomography (PET) radiotracer that has demonstrated promising results in the staging and restaging of prostate carcinoma, with high positive predictive value (PPV) in the identification of extraprostatic malignancy. Most of the prior studies of FACBC were in post-primary treatment recurrence, and this proposed trial will be the first comprehensive study to evaluate FACBC PET in detecting occult metastatic disease at initial diagnosis in patients with negative or equivocal conventional imaging, with the objective of developing a more effective primary treatment plan. The goal of this study is to determine if FACBC PET will detect significant occult metastatic disease in patients with high risk primary prostate carcinoma who have negative or equivocal conventional imaging such as CT and/or MRI and bone scan. Participants will have a single scan prior to surgery for this study. Participants will be followed, through medical record reviews, for 10 years but no additional procedures related to this study will be performed.

Interventions

DRUGFACBC PET-CT Imaging

Participants will fast for 4 hours to normalize their neutral amino acid levels. One hour prior to the scan, participants will drink up to 450ml of standard oral contrast. Participants will lie on the scanning bed while the bed moves through the PET/CT scanner for the CT portion of the exam. After completion of the CT scan, approximately 10 units of FACBC will be injected for the PET scan portion of the exam. The bed will move through the scanner again and the PET portion of the exam will take 30 minutes. The entire visit will take about two hours. Standard of care procedures include conventional imaging (CT and/or MRI; bone scan and/or NaF PET per institutional standards) and radical prostatectomy with extended pelvic lymph node dissection.

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
Emory University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

All participants will have the same intervention

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* High-risk prostate cancer patients eligible for standard of care surgery * At least clinical T3a disease, and/or Gleason≥8, and/or Prostate-Specific Antigen (PSA) \>20, as per clinical assessment and routine guidelines * Undergone standard of care conventional imaging (CT and/or MRI; bone scan and/or sodium fluoride (NaF) PET)

Exclusion criteria

* Definitive findings of systemic metastasis on conventional imaging.

Design outcomes

Primary

MeasureTime frameDescription
Cancer Detection Performance of FACBC PET/CTDay 1The performance of FACBC PET/CT for diagnosing metastatic cancer was determined by confirming the FACBC PET/CT findings to the histological analysis of the lymph nodes.

Secondary

MeasureTime frameDescription
Diagnostic Performance of FACBC PET/CT and Conventional ImagingDay 1, Day of surgeryThe diagnostic performance of FACBC PET/CT in the detection of extraprostatic disease is compared to the diagnostic performance of standard imaging, as confirmed with lymph node histology.

Countries

United States

Participant flow

Recruitment details

Participant enrollment began March 1, 2017 and all study follow-up was completed by December 31, 2019. Participants were enrolled from the patient population at Emory University Hospital in Atlanta, Georgia.

Participants by arm

ArmCount
FACBC PET-CT Imaging
Individuals diagnosed with primary prostate carcinoma and without definitive findings of systemic metastasis with conventional imaging, had a whole body FACBC positron emission tomography (PET)-computerized tomography (CT)(PET-CT) scan followed by robotic radical prostatectomy with extended pelvic lymph node dissection.
57
Total57

Withdrawals & dropouts

PeriodReasonFG000
Overall Studydeferred prostate cancer treatment1
Overall Studymetastasis managed with systemic therapy3

Baseline characteristics

CharacteristicFACBC PET-CT Imaging
Age, Continuous61.7 years
STANDARD_DEVIATION 7
Race and Ethnicity Not Collected— Participants
Region of Enrollment
United States
57 Participants
Sex: Female, Male
Female
0 Participants
Sex: Female, Male
Male
57 Participants
Type of Standard of Care Imaging
Computerized tomography (CT)
20 Participants
Type of Standard of Care Imaging
Magnetic resonance imaging (MRI)
37 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 57
other
Total, other adverse events
0 / 57
serious
Total, serious adverse events
0 / 57

Outcome results

Primary

Cancer Detection Performance of FACBC PET/CT

The performance of FACBC PET/CT for diagnosing metastatic cancer was determined by confirming the FACBC PET/CT findings to the histological analysis of the lymph nodes.

Time frame: Day 1

ArmMeasureCategoryValue (COUNT_OF_PARTICIPANTS)
FACBC PET-CT ImagingCancer Detection Performance of FACBC PET/CTTrue positive17 Participants
FACBC PET-CT ImagingCancer Detection Performance of FACBC PET/CTTrue negative22 Participants
FACBC PET-CT ImagingCancer Detection Performance of FACBC PET/CTFalse positive4 Participants
FACBC PET-CT ImagingCancer Detection Performance of FACBC PET/CTFalse negative14 Participants
Secondary

Diagnostic Performance of FACBC PET/CT and Conventional Imaging

The diagnostic performance of FACBC PET/CT in the detection of extraprostatic disease is compared to the diagnostic performance of standard imaging, as confirmed with lymph node histology.

Time frame: Day 1, Day of surgery

ArmMeasureGroupValue (NUMBER)
FACBC PET-CT ImagingDiagnostic Performance of FACBC PET/CT and Conventional ImagingSpecificity84.8 percentage of participants
FACBC PET-CT ImagingDiagnostic Performance of FACBC PET/CT and Conventional ImagingNegative predictive value60.8 percentage of participants
FACBC PET-CT ImagingDiagnostic Performance of FACBC PET/CT and Conventional ImagingPositive predictive value81.5 percentage of participants
FACBC PET-CT ImagingDiagnostic Performance of FACBC PET/CT and Conventional ImagingAccuracy68.5 percentage of participants
FACBC PET-CT ImagingDiagnostic Performance of FACBC PET/CT and Conventional ImagingSensitivity55.3 percentage of participants
Conventional ImagingDiagnostic Performance of FACBC PET/CT and Conventional ImagingAccuracy56.3 percentage of participants
Conventional ImagingDiagnostic Performance of FACBC PET/CT and Conventional ImagingSensitivity33.3 percentage of participants
Conventional ImagingDiagnostic Performance of FACBC PET/CT and Conventional ImagingSpecificity84.1 percentage of participants
Conventional ImagingDiagnostic Performance of FACBC PET/CT and Conventional ImagingPositive predictive value72.2 percentage of participants
Conventional ImagingDiagnostic Performance of FACBC PET/CT and Conventional ImagingNegative predictive value51.2 percentage of participants

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026