Genomic and Immune Landscape of Recurrent and/or Metastatic Squamous Cell Carcinoma of the Head and Neck Progressing on Anti-PD-1 Treatment.
Anti-PD-1 therapies improve survival in recurrent/metastatic (R/M) squamous cell carcinoma of the head and neck (SCCHN), but only a minority of patients achieve durable responses.
APA
van der Elst A, Herrero-Saboya D, et al. (2026). Genomic and Immune Landscape of Recurrent and/or Metastatic Squamous Cell Carcinoma of the Head and Neck Progressing on Anti-PD-1 Treatment.. Cancer immunology research, 14(4), 608-624. https://doi.org/10.1158/2326-6066.CIR-25-0979
MLA
van der Elst A, et al.. "Genomic and Immune Landscape of Recurrent and/or Metastatic Squamous Cell Carcinoma of the Head and Neck Progressing on Anti-PD-1 Treatment.." Cancer immunology research, vol. 14, no. 4, 2026, pp. 608-624.
PMID
41666253
Abstract
Anti-PD-1 therapies improve survival in recurrent/metastatic (R/M) squamous cell carcinoma of the head and neck (SCCHN), but only a minority of patients achieve durable responses. The mechanisms driving resistance to anti-PD-1 in SCCHN remain poorly understood. Using the IMMUcan multiomics workflow, we characterized the molecular and immune profiles of R/M SCCHN progressing on anti-PD-1 treatment and compared them with an anti-PD-1-naïve cohort. Tumor biopsies from patients with anti-PD-1-resistant SCCHN exhibited significantly more EGFR and MYCL amplifications, along with increased MYC pathway alterations. Transcriptomic and proteomic analyses revealed that anti-PD-1-secondary resistant SCCHN had increased CD8+ T-cell infiltration with higher levels of immune exhaustion markers than primary resistant and naïve SCCHN. Additionally, high beta-2-microglobulin (B2M) expression correlated with greater T-cell infiltration and improved survival following anti-PD-1 therapy. Tumor cell B2M expression was independent of TMB and PD-1L expression, suggesting that B2M expression could serve as an additional biomarker for anti-PD-1 response.
MeSH Terms
Humans; Squamous Cell Carcinoma of Head and Neck; Head and Neck Neoplasms; Programmed Cell Death 1 Receptor; Neoplasm Recurrence, Local; Immune Checkpoint Inhibitors; Female; Male; Middle Aged; Drug Resistance, Neoplasm; Aged; Biomarkers, Tumor; Genomics; CD8-Positive T-Lymphocytes