This study aims to evaluate the role of early response assessment by 18F-FDG PET/CT in patients with recurrent and/or metastatic (R/M) head and neck squamous cell carcinoma with PD-L1 CPS \>1 treated with pembrolizumab monotherapy, in accordance with routine clinical practice.
Eligible patients will receive two administrations of Pembrolizumab as monotherapy. An 18F-FDG PET/CT scan will be performed at baseline (T0; no more than 30 days before the first drug administration) and after two cycles (T1, at 6 weeks). Patients will be considered responders if they achieve a complete response (defined as complete resolution of FDG uptake within the target lesions) or a partial response (i.e., \>=30% decrease in the target tumor FDG SULpeak). After the first two administrations of Pembrolizumab, as well as in case of progressive disease (i.e., \>=30% increase in the target tumor FDG SULpeak or advent of new 18FDG-avid lesions), any treatment modification will be determined by the physician according to routine clinical practice
Study Type
OBSERVATIONAL
Enrollment
25
Tor Vergata University Hospital
Rome, Italy, Italy
RECRUITINGPredictive value of 18F-FDG PET/CT metabolic changes at 6 weeks for response to pembrolizumab
To evaluate whether changes in metabolic activity on 18F-FDG PET/CT at 6 weeks predict response to pembrolizumab monotherapy at 3, 6, and 9 months in patients with recurrent and/or metastatic head and neck squamous cell carcinoma (HNSCC).
Time frame: through study completion, an average of 1 year
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