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Identification of prognostic liquid biopsy biomarkers in patients with cutaneous squamous cell carcinoma treated with cemiplimab - Journal of Translational Medicine
Cemiplimab was administered to patients considered unsuitable for curative surgery or radiotherapy, as determined by a multidisciplinary team discussion. Cemiplimab was administered intravenously (IV) at a dose of 350 mg flat dose every 3 weeks. The clinical response was assessed radiologically according to the RECIST 1.1 criteria [23] or clinically according to the WHO criteria [24].
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