Immune Checkpoint Inhibitors for the Treatment of Periorbital Non-Melanoma Skin Cancers

Niloufar Bineshfar1, Leo Meller2, Andrew J Rong1

  • 1Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL, USA.

Seminars in Ophthalmology
|February 18, 2026
PubMed
Abstract

Insights

Anti-programmed death (PD-1)/PD-L1 immunotherapy shows promise for advanced periocular non-melanoma skin cancers (NMSCs). Cemiplimab was effective in treating basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) when other therapies failed.

Area of Science:

  • Oncology
  • Immunotherapy
  • Dermatology

Background:

  • Non-melanoma skin cancers (NMSCs) of the periocular region, including basal cell carcinoma (BCC) and squamous cell carcinoma (SCC), pose significant clinical challenges.
  • Locally advanced periocular NMSCs often require multimodal treatment approaches.

Purpose of the Study:

  • To evaluate the outcomes of anti-programmed death (PD-1)/PD-L1 immunotherapy in patients with locally advanced periocular NMSCs.
  • To assess the efficacy of immune checkpoint inhibitors in a challenging subset of skin cancer patients.

Main Methods:

  • A retrospective study analyzed nine patients with locally advanced periocular BCC or cutaneous SCC treated with anti-PD-1/PD-L1 agents between January 2016 and January 2023.
  • Patient records were reviewed for clinical and histological data, with therapy effectiveness evaluated.

Main Results:

  • Four patients had periocular BCC and five had cutaneous SCC; most had prior treatments.
  • Anti-PD-1/PD-L1 therapy was effective in two BCC and two SCC cases, with all responders treated using cemiplimab.
  • Treatments included cemiplimab, nivolumab, and pembrolizumab, with one patient receiving all three.

Conclusions:

  • Anti-PD-1/PD-L1 immunotherapy, particularly cemiplimab, is a promising treatment for locally advanced periocular BCC and SCC, especially after failure of traditional therapies.
  • Further research using larger cohorts and multi-institutional collaborations is warranted to validate these findings and explore adjuvant immunotherapy roles.

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