Abstract
Recent studies have evidenced the potential of combining anti-EGFR therapies with anti-PD-1/PD-L1 checkpoint therapies. Both anti-EGFR and anti-PD-1/PD-L1 have been separately tested in the treatment of cutaneous SCC (cSCC). Here, we review recent data on EGFR in the context of cancer progression, as a prognostic and as a therapeutic target in cSCC. Anti-EGFR/checkpoint immunotherapy and other combination therapy approaches are discussed. With the advent of immunotherapy, EGFR is still a valid cSCC target.
Keywords:
Epidermal growth factor receptor (EGFR); Programmed death ligand 1 (PD-L1); Squamous cell carcinoma (SCC); Therapy.
MeSH terms
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Antineoplastic Agents, Immunological / pharmacology
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Antineoplastic Agents, Immunological / therapeutic use
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Biomarkers, Tumor*
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Carcinoma, Squamous Cell / drug therapy
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Carcinoma, Squamous Cell / etiology*
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Carcinoma, Squamous Cell / metabolism*
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Carcinoma, Squamous Cell / pathology
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Clinical Trials as Topic
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Disease Management
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Disease Susceptibility
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ErbB Receptors / antagonists & inhibitors
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ErbB Receptors / genetics
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ErbB Receptors / metabolism
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Humans
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Immune Checkpoint Proteins / genetics
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Immune Checkpoint Proteins / metabolism
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Immunotherapy
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Molecular Targeted Therapy
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Prognosis
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Skin Neoplasms / drug therapy
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Skin Neoplasms / etiology*
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Skin Neoplasms / metabolism*
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Skin Neoplasms / pathology
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Treatment Outcome
Substances
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Antineoplastic Agents, Immunological
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Biomarkers, Tumor
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Immune Checkpoint Proteins
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EGFR protein, human
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ErbB Receptors