PET Imaging Agent for Head and Neck Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new PET imaging agent to enhance the diagnosis of head and neck squamous cell carcinoma (HNSCC), particularly when current scans are unclear. The researchers aim to determine if this agent can more accurately identify cancerous areas, reducing unnecessary biopsies and improving treatment planning. Participants will receive cetuximab, a known targeted therapy, before using the new agent for imaging. The trial seeks individuals with head and neck cancer who have unclear results from standard imaging tests. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, offering participants the opportunity to be among the first to receive this new imaging agent.
Do I have to stop taking my current medications for the trial?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
What prior data suggests that this PET imaging agent is safe for patients with head and neck cancer?
Research has shown that the PET imaging agent \[18F\]NOTA-ABY030 is undergoing testing for safety in humans. The main goal is to evaluate its effectiveness and safety. This agent aims to help doctors see tumors more clearly on scans. Researchers are closely monitoring its safety, but detailed safety information remains limited due to the early stage of research.
This trial is in its first phase, focusing primarily on safety. Researchers are studying how the body processes the agent and identifying any side effects. It is important to note that any new drug or agent begins with these early tests to ensure safety before progressing to larger studies. As research continues, more safety information will become available.12345Why are researchers excited about this trial?
Researchers are excited about this trial because it uses a PET imaging agent, [18F]NOTA-ABY-030, to enhance the diagnostic capabilities for head and neck cancer. Unlike traditional imaging methods, which may struggle to clearly identify metastatic or primary lesions, this agent is designed to improve sensitivity and specificity in detecting cancerous cells. The trial also aims to optimize the timing and dosage of this imaging agent, potentially leading to more accurate and safer diagnostic protocols for patients with head and neck squamous cell carcinoma. This could be a game-changer in diagnosing and monitoring this type of cancer more effectively.
What evidence suggests that this PET imaging agent is effective for head and neck cancer?
Research has shown that [18F]NOTA-ABY-030 is a promising new tool for PET scans used to examine head and neck cancer. This trial will evaluate [18F]NOTA-ABY-030 in combination with cetuximab. The imaging agent targets a protein called EGFR, which aids cancer cell growth, and reduces background noise in images, potentially making tumors easier to see. Early results suggest this tool could outperform traditional methods like CT or MRI scans in tumor detection. This improvement could help doctors make better treatment decisions and reduce unnecessary procedures like biopsies. While data collection continues, the tool's design suggests it could be more effective in identifying cancerous areas.678910
Who Is on the Research Team?
Eben Rosenthal, MD
Principal Investigator
Vanderbilt University Medical Center
Are You a Good Fit for This Trial?
This trial is for patients with head and neck squamous cell carcinoma who have unclear results from standard imaging. Participants must be suitable for PET/CT scans and willing to receive a cetuximab loading dose before the investigational imaging agent.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive a loading dose of cetuximab followed by [18F]NOTA-ABY030, with PET/CT imaging performed at defined intervals to assess biodistribution and lesion uptake
Follow-up
Participants are monitored for safety and effectiveness after treatment
Long-term Follow-up
Participants are monitored for diagnostic performance and comparison with standard imaging modalities
What Are the Treatments Tested in This Trial?
Interventions
- 18F-NOTA-ABY-030
- Cetuximab
Find a Clinic Near You
Who Is Running the Clinical Trial?
Vanderbilt-Ingram Cancer Center
Lead Sponsor