Dynamic Changes in Circulating Tumor DNA During Immunotherapy for Head and Neck Cancer: SHIZUKU-HN Study

Rika Noji1,2, Kohki Tohyama3, Shin Nakamura3

  • 1Department of Oral and Maxillofacial Surgical Oncology, Division of Health Science, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, 1-5-45 Yushima, Bunkyo-Ku, Tokyo 113-8510, Japan.

Insights

Circulating tumor DNA (ctDNA) shows promise as a real-time biomarker for monitoring head and neck squamous cell carcinoma (HNSCC) treatment response to immune checkpoint inhibitors (ICIs). ctDNA analysis, particularly variant allele frequency (VAF), correlates with tumor volume and can precede radiographic progression, aiding personalized therapy.

Area of Science:

  • Oncology
  • Molecular Diagnostics
  • Biomarker Research

Background:

  • Immune checkpoint inhibitors (ICIs) show limited durable response rates (20%) in recurrent/metastatic head and neck squamous cell carcinoma (HNSCC).
  • Circulating tumor DNA (ctDNA) has emerged as a potential non-invasive biomarker for cancer monitoring.
  • Current utilization of ctDNA testing in HNSCC is low (7% in Japan's C-CAT database).

Purpose of the Study:

  • To evaluate ctDNA as a real-time biomarker for monitoring treatment response in HNSCC patients receiving ICIs.
  • To correlate ctDNA dynamics with tumor volume and radiographic changes.
  • To identify genetic mutations via ctDNA that may indicate treatment resistance.

Main Methods:

  • Prospective analysis of serial plasma samples from 27 HNSCC patients undergoing ICIs (SHIZUKU-HN study).
  • Guardant360 assay used to assess ctDNA variant allele frequency (VAF) and genetic mutations.
  • Tumor volume quantified using 3D CT reconstruction; comparison with Japan's C-CAT database (n=2255).

Main Results:

  • Mean ctDNA VAF significantly correlated with tumor volume (Spearman's ρ = 0.70, p = 0.001).
  • ctDNA changes often preceded radiographic progression, indicating early treatment response or resistance.
  • Disappearance of BRAF/APC mutations in partial responders and detection of EGFR/PIK3CA amplifications via ctDNA suggested resistance mechanisms.

Conclusions:

  • ctDNA serves as a dynamic and sensitive biomarker for real-time monitoring of HNSCC treatment response to ICIs.
  • ctDNA analysis provides early insights into treatment efficacy and can identify emerging resistance mechanisms.
  • This approach supports personalized ICI therapy strategies for HNSCC patients.

Related Concept Videos