# Effectiveness and safety of cemiplimab in locally advanced and metastatic cutaneous squamous cell carcinoma

**Authors:** Gabriele Roccuzzo, Eleonora Bongiovanni, Giovanni Actis-Giorgetto, Chiara Astrua, Matteo Giovanni Brizio, Giovanni Cavaliere, Paolo Fava, Simone Ribero, Pietro Quaglino

PMC · DOI: 10.3389/fphar.2026.1601650 · 2026-03-06

## TL;DR

This study shows cemiplimab is effective and safe for treating advanced skin cancer, with half of patients responding positively, though some experienced side effects.

## Contribution

The study provides real-life evidence of cemiplimab's effectiveness and safety in treating locally advanced and metastatic cutaneous squamous cell carcinoma.

## Key findings

- Cemiplimab achieved a 49.4% objective response rate in patients with advanced skin cancer.
- Median overall survival was 19 months, and half of patients experienced adverse events.
- Patients with head and neck tumors had longer survival after first progression.

## Abstract

Cutaneous squamous cell carcinoma (cSCC) is a common skin cancer with increasing incidence. The anti-PD-1 therapy cemiplimab has shown its antitumor activity in locally advanced (lacSCC) and metastatic cSCC (mcSCC). This retrospective study assessed the real-life effectiveness and safety of cemiplimab in 83 patients with lacSCC (n = 53) and mcSCC (n = 30). The objective response rate (ORR) was 49.4%, with a complete response (CR) in 15.7% and a partial response (PR) in 33.7%. The median progression-free survival (PFS) was 14 months (95% CI 9–55) and the median overall survival (OS) 19 months (95% CI 10–39). Half of patients (50.6%) experienced adverse events (AE) of any grade, with 8.4% discontinuing therapy due to the severe AEs. The subset of patients who experienced progression during therapy displayed younger age (p = 0.002), a higher disease stage at baseline (p = 0.003), and a nodal disease (p = 0.041). No differences in survival outcome emerged between patients with nodal vs. distant metastases, previous radiotherapy recipient vs. radiotherapy-naïve, and immunosuppressed vs. immunocompetent patients. Head&neck tumor site was associated with a longer OS after first progression (OS2, HR 0.29, 95% CI 0.09–0.89). This study supports the safe and effective use of cemiplimab in real life clinical practice yet highlights the need for further identification of new predictors of clinical response.

## Linked entities

- **Diseases:** cutaneous squamous cell carcinoma (MONDO:0002529)

## Full-text entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}
- **Diseases:** Cutaneous squamous cell carcinoma (MESH:D002294), Head&amp;neck tumor (MESH:D006258), nodal (MESH:D013611), skin cancer (MESH:D012878), metastases (MESH:D009362), nodal disease (MESH:D004194)
- **Chemicals:** cemiplimab (MESH:C000627974)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13002820/full.md

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Source: https://tomesphere.com/paper/PMC13002820