Monotherapy With Immune Checkpoint Inhibitors in Patients With Recurrent and/or Metastatic Sinonasal Squamous Cell

Alexander Lein1, Thorsten Fuereder2, Manuel Stoeth3

  • 1Department of Otorhinolaryngology, Head and Neck Surgery, Medical University of Vienna, Vienna, Austria.

Cancer Medicine
|November 27, 2025
PubMed
Abstract

Insights

Immune checkpoint inhibitors (ICIs) show potential for recurrent and/or metastatic sinonasal squamous cell carcinoma (SNSCC). This study found immunotherapy offers a possible treatment option, though larger trials are needed for this rare cancer.

Area of Science:

  • Oncology
  • Immunotherapy
  • Head and Neck Cancers

Background:

  • Sinonasal squamous cell carcinoma (SNSCC) is a rare cancer with limited treatment options for recurrent or metastatic (r/m) disease.
  • Immune checkpoint inhibitors (ICIs) are effective in other head and neck cancers, but their role in SNSCC is not well-defined.
  • SNSCC patients are often excluded from clinical trials, hindering evidence generation for ICI efficacy.

Purpose of the Study:

  • To evaluate the efficacy and safety of single-agent ICI therapy in patients with r/m SNSCC.
  • To compare outcomes in r/m SNSCC patients treated with ICIs to those with other head and neck squamous cell carcinomas.

Main Methods:

  • A retrospective multicenter analysis of 18 r/m SNSCC patients treated with single-agent Pembrolizumab or Nivolumab from July 2018 to December 2023.
  • Exploratory comparison with a cohort of 121 patients with r/m squamous cell carcinoma of the larynx, oropharynx, hypopharynx, or oral cavity.

Main Results:

  • The overall response rate (ORR) was 11.1%, disease control rate (DCR) was 27.8%, with a median progression-free survival (PFS) of 11.7 months and overall survival (OS) of 18.9 months.
  • High pathological grading was a negative prognostic factor for PFS (p=0.049).
  • Outcomes in SNSCC were broadly similar to other head and neck cancers, with no statistically significant differences in PFS, OS, ORR, or DCR.

Conclusions:

  • Single-agent immunotherapy may be a viable treatment option for r/m SNSCC.
  • The limited sample size necessitates cautious interpretation of findings.
  • Future prospective trials should include SNSCC patients to clarify the role of immunotherapy in this underrepresented population.

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