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Monotherapy with immune checkpoint inhibitors in patients with recurrent and/or metastatic sinonasal squamous cell carcinoma
Department of Otorhinolaryngology, Head and Neck Surgery, Medical University of Vienna, Vienna, Austria.
Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital Würzburg, Würzburg, Germany.
Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital Würzburg, Würzburg, Germany.
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2025 (English)In: Cancer Medicine, E-ISSN 2045-7634, Vol. 14, no 23, article id e71391Article in journal (Refereed) Published
Abstract [en]

Introduction: Sinonasal squamous cell carcinoma (SNSCC) is a rare malignancy with limited data on effective treatment modalities in the recurrent and/or metastatic (r/m) setting. While immune checkpoint inhibitors (ICIs) have shown promise in treating head and neck cancers, in general, their effects in SNSCC remain poorly understood. Furthermore, SNSCC patients are frequently excluded from clinical trials, limiting the evidence base for ICI efficacy in this specific subgroup. Therefore, our study evaluated the efficacy and safety of single-agent ICI therapy in r/m SNSCC.

Methods: We conducted a retrospective multicenter analysis of all r/m SNSCC patients treated with single-agent ICIs from July 2018 to December 2023 at two tertiary reference centers.

Results: A total of 18 patients received either Pembrolizumab (n = 8) or Nivolumab (n = 10) for r/m SNSCC. The overall response rate (ORR) to immunotherapy was 11.1% (2/18), with a disease control rate (DCR) of 27.8% (5/18) and a mean PFS and OS of 11.7 (95% CI: 2.3–21.0) months and 18.9 (95% CI: 8.3–29.5) months respectively. Two (11.1%) immune-related adverse events led to treatment discontinuation. Univariable analysis revealed high pathological grading (p = 0.049) as a negative prognostic factor for PFS. In an exploratory comparison with a larger cohort of 121 patients with r/m SCC of the larynx, oropharynx, hypopharynx, or oral cavity receiving ICI therapy, outcomes in SNSCC appeared broadly similar, with no statistically significant differences in PFS (p = 0.153), OS (p = 0.152), ORR (p = 0.401), or DCR (p = 0.359).

Conclusion: Immunotherapy may represent a treatment option for patients with SNSCC. Given the limited sample size, these results should be interpreted with caution. Our findings highlight the urgent need to include SNSCC patients in future prospective trials to clarify the role of immunotherapy in this underrepresented population.

Place, publisher, year, edition, pages
John Wiley & Sons, 2025. Vol. 14, no 23, article id e71391
Keywords [en]
advanced disease, head and neck cancer, immune-checkpoint therapy, sinonasal squamous cell carcinoma
National Category
Cancer and Oncology
Identifiers
URN: urn:nbn:se:umu:diva-247466DOI: 10.1002/cam4.71391ISI: 001625166200001PubMedID: 41308007Scopus ID: 2-s2.0-105023334275OAI: oai:DiVA.org:umu-247466DiVA, id: diva2:2021500
Available from: 2025-12-15 Created: 2025-12-15 Last updated: 2025-12-15Bibliographically approved

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Kenner, Lukas

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