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RecruitingInterventional

Use of [F-18] FLT for Imaging With Positron Emission Tomography (PET)

NCT ID: NCT00935090Sponsor: Barbara Ann Karmanos Cancer InstituteLast updated: 2025-07-08

Summary

RATIONALE: Diagnostic procedures, such as 3'-deoxy-3'-\[18F\] fluorothymidine (FLT) PET imaging, may help find and diagnose cancer. It may also help doctors predict a patient's response to treatment and help plan the best treatment. PURPOSE: This phase I trial is studying FLT PET imaging in patients with cancer.

Detailed description

OBJECTIVES: Primary * Evaluate the use of 3'-deoxy-3'-\[18F\] fluorothymidine (FLT) positron emission tomography (PET) imaging to measure tumor proliferation and the DNA synthetic pathway (thymidine kinase levels) in patients with cancer. Secondary * Determine the efficacy of FLT PET imaging in detecting lesions and estimating response to treatment. OUTLINE: Patients undergo up to four 3'-deoxy-3'-\[18F\] fluorothymidine positron emission tomography imaging procedures.

Arms & interventions

  • Device3'-deoxy-3'-[18F]fluorothymidine

    The tracer compound \[F-18\] FLT will be injected into the patient's veins in a small volume of normal saline solution. The PET scan data collection is started immediately and is continued for 2 hours. This procedure will measure tumor growth within the body. Blood may be withdrawn (through the catheters) up to a total volume of 30 milliliters (or 2 tablespoons) for each scan. A urine sample may be collected at the end of the imaging of the tracer compound to analyze its breakdown products.

Outcome measures

Primary

  • Measurement of the uptake and retention of 3'-deoxy-3'-[18F] fluorothymidine (FLT) in tumors and normal organs

    Time frame: at time of PET or CT PET Scan

  • Changes in thymidine kinase, thymidylate synthase, and standardized uptake values

    Time frame: before and after therapy

Secondary

  • FLT PET response rate

    Time frame: up to 2 hours during PET scan

Eligibility criteria

Sex: AllAge: 18 Years to 120 YearsHealthy volunteers: No
DISEASE CHARACTERISTICS: * Meets one of the following criteria: * Histologically confirmed solid tumor or hematologic malignancy * Awaiting biopsy or surgery for cancer evaluation of a mass detected on exam or standard imaging PATIENT CHARACTERISTICS: * Able to lie still in the PET scanner * Girth and weight must be suitable to enter the gantry * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: * Not specified

Study locations (1)

Barbara Ann Karmanos Cancer Institute

Detroit, Michigan, 48201-1379

Recruiting
Clinical Trials Office - Barbara Ann Karmanos Cancer Institute · Contact
Elisabeth Heath, M.D. · Sub Investigator
Otto Muzik, Ph.D. · Sub Investigator
Mohammed N Al Hallak, M.D · Sub Investigator
Hirva Mamdani, M.D · Sub Investigator
Ammar Sukari, M.D. · Sub Investigator
Huailei Jiang, Ph.D. · Sub Investigator