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High-risk cutaneous squamous cell carcinoma: a review of current evidence and emerging standards

Published online by Cambridge University Press:  19 January 2026

Fausto Petrelli
Affiliation:
Oncology Unit, ASST Bergamo Ovest, Treviglio (BG), Italy
Elisa Dal Cin
Affiliation:
Otorhinolaryngology Unit, Head and Neck Department, Mestre Hospital, Venice, Italy
Daniela Carioli
Affiliation:
Otorhinolaryngology Unit, ASST Bergamo Ovest, Treviglio (BG), Italy
Angela Gasparini
Affiliation:
Otorhinolaryngology Unit, ASST Bergamo Ovest, Treviglio (BG), Italy
Chiara Bramati
Affiliation:
Otorhinolaryngology Unit, ASST Bergamo Ovest, Treviglio (BG), Italy
Daniele Spada
Affiliation:
Otorhinolaryngology Unit, ASST Bergamo Ovest, Treviglio (BG), Italy
Massimiliano Nardone
Affiliation:
Otorhinolaryngology Unit, ASST Bergamo Ovest, Treviglio (BG), Italy
Vincenzo Capriotti*
Affiliation:
Otorhinolaryngology Unit, AULSS 3 Serenissima, Ospedale di Mirano, Venice, Italy
*
Corresponding author: Vincenzo Capriotti; Email: capriotti.orl@gmail.com

Abstract

Objective

High-risk cutaneous squamous cell carcinoma represents 3–5 per cent of all cutaneous squamous cell carcinomas but causes most disease-specific deaths. Head and neck tumours are often high risk. Recent phase-3 trials have challenged surgery plus or minus radiotherapy as standards of care. This review updates definitions and evidence on emerging treatments.

Methods

Narrative review.

Results

High-risk cutaneous squamous cell carcinoma is defined by size greater than 2 cm, deep invasion, poor differentiation, perineural/lymphovascular invasion, nodal spread or immunosuppression. Surgery remains central, with adjuvant radiotherapy improving locoregional control. The KEYNOTE-630 trial of adjuvant pembrolizumab showed a non-significant recurrence-free survival gain (hazard ratio 0.76), with benefit in elderly and extracapsular extension subgroups. The C-POST trial established adjuvant cemiplimab as the first systemic therapy significantly improving disease-free survival (hazard ratio 0.32; 24-month disease-free survival 87 per cent vs 64 per cent). Emerging strategies include neoadjuvant programmed cell-death protein 1 blockade, circulating tumour DNA-guided monitoring and combinations.

Conclusions

Cemiplimab redefines the post-operative standard; pembrolizumab awaits confirmation. Future directions include earlier immunotherapy, biomarker validation and access expansion.

Information

Type
Review Article
Copyright
© The Author(s), 2026. Published by Cambridge University Press on behalf of J.L.O. (1984) LIMITED.

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