Actively Recruiting

Age: 18Years +
All Genders
ID07417605

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

On this page

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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)

Long-term Monitoring

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

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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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