18F-FMAU PET/CT in Imaging Patients With Advanced Cancers

Sponsor
University of Southern California (Other)
Overall Status
Recruiting
CT.gov ID
NCT02079181
Collaborator
National Cancer Institute (NCI) (NIH)
30
1
1
132
0.2

Study Details

Study Description

Brief Summary

This clinical trial studies the safety and drug distribution of the radioactive drug, 2'-deoxy-2'-[18F]fluoro-5-methyl-1-beta-D-arabinofuranosyluracil (fluorine F 18 d-FMAU [18F-FMAU]), for imaging with positron emission tomography/computed tomography (PET/CT) in patients with advanced cancers. A PET scan is a procedure in which a small amount of radioactive glucose (sugar) is injected into a vein, and a scanner is used to make detailed, computerized pictures of areas inside the body where the glucose is taken up. Because cancer cells often take up more glucose than normal cells, the pictures can be used to find cancer cells in the body. PET/CT using the drug fluorine F 18 d-FMAU, may help find cancer and find out how far the disease has spread.

Condition or Disease Intervention/Treatment Phase
  • Radiation: fluorine F 18 d-FMAU
  • Procedure: positron emission tomography
  • Procedure: computed tomography
N/A

Detailed Description

PRIMARY OBJECTIVES:
  1. To determine the radiation dosimetry of 18F-FMAU in humans, confirm absence of adverse events in humans from intravenous (i.v.) injection of 18F-FMAU for PET imaging, and characterize the incidence of circulating metabolites of 18F-FMAU in humans.

  2. To simply find out whether there is any visual uptake change of 18F-FMAU in tumors post-therapy.

OUTLINE:

Patients receive fluorine F 18 d-FMAU IV followed by PET/CT prior to start of cancer treatment. Patients may undergo 2 additional scans at one week prior to second course of chemotherapy and after completion of cancer treatment depending on cancer type.

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:
18F-FMAU for Imaging in Cancer Patients
Actual Study Start Date :
Jan 31, 2014
Anticipated Primary Completion Date :
Jan 31, 2024
Anticipated Study Completion Date :
Jan 31, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Diagnostic (fluorine F 18 d-FMAU PET/CT scan)

Patients receive fluorine F 18 d-FMAU IV followed by PET/CT prior to start of cancer treatment. Patients may undergo 2 additional scans at one week prior to second course of chemotherapy and after completion of cancer treatment depending on cancer type.

Radiation: fluorine F 18 d-FMAU
Given IV

Procedure: positron emission tomography
Undergo fluorine F 18 d-FMAU PET/CT scan
Other Names:
  • FDG-PET
  • PET
  • PET scan
  • tomography, emission computed
  • Procedure: computed tomography
    Undergo fluorine F 18 d-FMAU PET/CT scan
    Other Names:
  • tomography, computed
  • Outcome Measures

    Primary Outcome Measures

    1. Radiation dosimetry of fluorine F 18 d-FMAU [Up to 24 hours after fluorine F 18 d-FMAU PET/CT scan]

    2. Adverse events after injection of fluorine F 18 d-FMAU to the patients [Up to 24 hours after fluorine F 18 d-FMAU PET/CT scan]

    3. Fluorine F 18 d-FMAU uptake change in tumors post-therapy [Baseline up to 24 hours after fluorine F 18 d-FMAU PET/CT scan]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    19 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Have been diagnosed with a malignancy/tumor/cancer, including but not limited to: brain tumor, breast cancer, lung cancer, esophageal cancer, lymphoma, or sarcoma

    • Have one or more tumors visualized by conventional PET-CT, CT or magnetic resonance imaging (MRI) prior to the PET FMAU study; PET-CT should be within one week prior to 18F-FMAU

    Exclusion Criteria:
    • Have undergone chemotherapy or radiation therapy within the previous one month

    • Women of childbearing potential, unless they have had a negative urine beta human chorionic gonadotropin (betaHCG) within the previous 24 hours of the procedure

    • Patients who have had surgery at the site of the suspected lesion within 1 month

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 USC Norris Comprehensive Cancer Center Los Angeles California United States 90033

    Sponsors and Collaborators

    • University of Southern California
    • National Cancer Institute (NCI)

    Investigators

    • Principal Investigator: Peter Conti, MD, University of Southern California

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Southern California
    ClinicalTrials.gov Identifier:
    NCT02079181
    Other Study ID Numbers:
    • 0S-12-3
    • NCI-2014-00314
    • 0S-12-3
    • P30CA014089
    First Posted:
    Mar 5, 2014
    Last Update Posted:
    Aug 9, 2022
    Last Verified:
    Aug 1, 2022
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 9, 2022