Evaluation of Fluciclovine Uptake in Patients With Cervical, Ovarian Epithelial or Endometrial Cancers.

Sponsor
Bital Savir-Baruch (Other)
Overall Status
Unknown status
CT.gov ID
NCT03349463
Collaborator
Blue Earth Diagnostics (Industry)
30
1
1
24.6
1.2

Study Details

Study Description

Brief Summary

An important part of staging and deciding the method of treatment is knowing areas of how cancer is involved. Diagnostic imaging is often used to determine the location of the cancer using techniques like nuclear medicine, MRI (magnetic resonance imaging), CT (computerized tomography), and ultrasound. Each technique looks for cancer in different ways and are often used together to make a better determination of the extent of disease.

One of the techniques used in cancer imaging is PET/CT. This technique combines a nuclear medicine study (PET or positron emission tomography) with CT performing both scans at the same time. PET/CT most commonly uses a radioactive sugar (FDG or fluorodeoxyglucose) to detect the cancer. The problem with FDG is that it is excreted by the kidneys and collected in the bladder. Even though the bladder is emptied prior to the scan, the FDG activity present there may interfere with the detection of small areas of cancer involvement in lymph nodes or adjacent areas. It is because of this that PET/CT using FDG is infrequently used in gynecological cancers.

This purpose of this study is to evaluate if 18F-fluciclovine can be used to help determine the extent of gynecological cancers. 18F-fluciclovine (also known as AXUMIN) is a radioactive tracer which has been approved by the FDAFood and Drug Administration (FDA) for use in patients with prostate cancer. 18F-fluciclovine has much less excretion through the kidneys which improves the PET/CT imaging of the pelvis.

Condition or Disease Intervention/Treatment Phase
  • Drug: Fluciclovine F18
Phase 4

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Evaluation of Fluciclovine Uptake in Patients With Cervical, Ovarian Epithelial or Endometrial Cancers. Pilot Study.
Actual Study Start Date :
Nov 14, 2018
Anticipated Primary Completion Date :
Dec 1, 2020
Anticipated Study Completion Date :
Dec 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: 18F-Fluciclovine

Drug: Fluciclovine F18
All study participants will receive 10 mCi of 18F-Fluciclovine (Axumin) one time administered through injection through the catheter into participant's arm immediately before PET/CT scan.
Other Names:
  • Axumin
  • anti-3-[18F] FACBC
  • Outcome Measures

    Primary Outcome Measures

    1. 18F-Fluciclovine uptake in gynecologic neoplasms [Day 30]

      PET/CT imaging

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • GYN cancer (ovarian, endometrial, or cervical) was biopsy-proven and/or schedule for subsequent surgery based on clinical presentation (imaging, markers)

    • Age ≥ 18 years.

    • Can tolerate 18F-fluciclovine PET/CT exam (can lie on her back for the duration of the scan).

    • Ability to understand and the willingness to sign a written informed consent.

    Exclusion Criteria:
    • Ongoing systemic therapy for cancer

    • Systemic therapy for cancer in the past 3 months

    • Inability to tolerate 18F-fluciclovine PET/CT exam

    • Pregnant or lactating women

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Loyola University Medical Center Maywood Illinois United States 60153

    Sponsors and Collaborators

    • Bital Savir-Baruch
    • Blue Earth Diagnostics

    Investigators

    • Principal Investigator: Bital Savir-Baruch, M.D, Nuclear Medicine Assistant Professor

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Bital Savir-Baruch, Nuclear Medicine Assistant Professor, Loyola University
    ClinicalTrials.gov Identifier:
    NCT03349463
    Other Study ID Numbers:
    • 209877
    First Posted:
    Nov 21, 2017
    Last Update Posted:
    Feb 28, 2020
    Last Verified:
    Feb 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 28, 2020