Actively Recruiting
Diagnostic Performance of 4D Dynamic LAFOV FDG-PET Imaging for Differentiating Residual Disease and Post-Radiation Inflammation in Head and Neck Squamous Cell Carcinoma Treated by Radiotherapy
Led by University Hospital, Brest · Updated on 2026-04-22
180
Participants Needed
1
Research Sites
N/A
Total Duration
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AI-Summary
What this Trial Is About
Researchers are investigating the use of dynamic FDG-PET LAFOV imaging to distinguish between remaining cancer and inflammation caused by radiation treatment in patients with head and neck squamous cell carcinoma. This observational study focuses on evaluating imaging results at three months after completing curative radiotherapy. The study aims to improve the accuracy of therapeutic assessment in this patient group. Participants will undergo a dynamic 4D LAFOV FDG-PET scan three months after finishing their radiotherapy treatment. This advanced imaging technique collects detailed metabolic data to help identify whether residual disease or post-radiation inflammation is present. The study does not include any treatment interventions but monitors imaging and pathology characteristics related to the cancer and treatment response. During the study, patients will be assessed at three months post-radiotherapy with FDG-PET imaging and followed up for up to twelve months to record imaging dates, disease progression, and survival status. Researchers will analyze various imaging parameters including Ki and DV values derived from Patlak reconstruction methods. They will also collect data on tumor pathology and any post-radiation toxicity. The study participation involves monitoring and evaluation without additional therapeutic procedures.
CONDITIONS
Brief Title
Diagnostic Performance Of 4D Dynamic LAFOV FDG-PET Acquisition for Differentiation of Residual Disease and Post-radiation Inflammation in Head Neck SCC Treated by Radiotherapy.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patient 18 years of age or older
- Diagnosed with head and neck squamous cell carcinoma
- Completed curative external radiation therapy treatment
- Eligible for dynamic LAFOV FDG-PET scan at 3 months for therapeutic evaluation
- Provided consent for end-of-treatment consultation
You will not qualify if you...
- Known hypersensitivity to 18F-FDG or related contrast agent components
- Pregnant or breastfeeding women
- History of treated upper gastrointestinal tract cancer
- Cancer with histology other than squamous cell carcinoma
- Incomplete radiotherapy treatment regimen
- Refusal to participate in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo a dynamic LAFOV FDG-PET scan at 3 months post-curative radiotherapy to differentiate residual disease from post-radiation inflammation.
1 visit (in-person)
Duration - Up to 12 months
Participants are monitored for progression, survival, and post-radiation toxicity up to 12 months after the FDG-PET imaging.
Follow-up visits as needed
Trial Site Locations
Total: 1 location
1
CHU Brest
Brest, France, 29200
Actively Recruiting
Research Team
R
Ronan ABGRAL, Pr
J
Jean-Christophe LECLERE, Dr
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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