Using FLT PET imaging to assess cancer in patients

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

Interventional Barbara Ann Karmanos Cancer Institute · NCT00935090

This study is testing a new type of PET imaging to see if it can help doctors better detect cancer and understand how well treatments are working for patients with different kinds of cancer.

Quick facts

Study typeInterventional
Ages18 Years to 120 Years
SexAll
SponsorBarbara Ann Karmanos Cancer Institute Academic / other
Locations1 site (Detroit, Michigan)
Trial IDNCT00935090 on ClinicalTrials.gov

What this trial studies

This clinical trial evaluates the effectiveness of 3'-deoxy-3'-[18F] fluorothymidine (FLT) positron emission tomography (PET) imaging in patients diagnosed with various types of cancer, including brain tumors and hematologic malignancies. The primary objective is to measure tumor proliferation and the levels of thymidine kinase, which are indicative of DNA synthesis in cancer cells. Additionally, the study aims to determine how well FLT PET imaging can detect cancer lesions and assess patient responses to treatment. Participants will undergo up to four imaging procedures to gather data on the efficacy of this diagnostic method.

Who should consider this trial

Good fit: Ideal candidates include adults with histologically confirmed solid tumors or hematologic malignancies who are awaiting further evaluation.

Not a fit: Patients who are not able to lie still in the PET scanner or those who are pregnant or nursing may not benefit from this study.

Why it matters

Potential benefit: If successful, this imaging technique could enhance the ability to diagnose cancer and tailor treatment plans more effectively for patients.

How similar studies have performed: Previous studies using PET imaging for cancer diagnosis have shown promising results, indicating that this approach may be effective.

Eligibility criteria

Show full inclusion / exclusion criteria
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

Where this trial is running

Detroit, Michigan

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Brain and Central Nervous System TumorsChronic Myeloproliferative DisordersLeukemiaLymphomaLymphoproliferative DisorderMultiple Myeloma and Plasma Cell NeoplasmMyelodysplastic SyndromesMyelodysplastic/Myeloproliferative Neoplasms
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.