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Data · dataset · 2026

Circulating tumour DNA kinetics in recurrent/metastatic head & neck squamous cell sarcinoma (R/M HNSCC) patients

Listed in ZivaHub and Deakin Research Online and DMU Figshare — shown once because both records carry DOI 10.17034/32805257.v1

Immune checkpoint blockade (ICB) has become a standard-of-care in the treatment of recurrent/metastatic head and neck squamous cell cancer (R/M HNSCC).

Description

However, only a subset of patients benefit from treatment and as such there is an urgent need to identify prognostic and predictive biomarkers of response to aid clinical decision-making. This work aims to evaluate clinicopathological features of R/M HNSCC, including markers of systemic inflammation and circulating tumour (ctDNA) kinetics under treatment selection pressure.<br><br>Patients and methods<br>R/M HNSCC patients treated with systemic therapy, platinum-based chemotherapy or ICB, underwent longitudinal blood sampling.

Biomarkers tested included ctDNA, measured by CAncer Personalized Profiling by deep Sequencing (CAPP-Seq) and markers of host inflammation, measured by neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR).<br><br>Results<br>Among 53 eligible patients, 16 (30%) received chemotherapy, 30 (57%) ICB [anti-PD1/L1] monotherapy and 7 (13%) combination immunotherapy. Median progression-free (PFS) and overall survival (OS) were 2.8 months (95% CI 1.3-4.3) and 8.2 months (95% CI 5.6-10.8), respectively.

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Seven (13%) patients experienced a partial response and 21 (40%) derived clinical benefit.<br><br>At baseline, median ctDNA variant allele frequency (VAF) was 4.3%. Baseline ctDNA abundance was not associated with OS (p=0.56) nor PFS (p=0.54). However, a change in ctDNA VAF after one cycle of treatment (ΔVAF (T1-2)) was predictive of both PFS (p<0.01) and OS (p<0.01).

Additionally, decrease in ΔVAF identified patients with longer OS despite early radiological progression, 8.2 vs 4.6 months, HR 0.44 (95% CI 0.19–0.87) p=0.03. At baseline, pre-treatment peripheral blood NLR and PLR are prognostic of PFS and OS. After incorporating NLR and PLR into multivariable Cox models, ctDNA ΔVAF retained an association with OS.<br><br>Conclusions<br>Early dynamic changes in ctDNA abundance, after one cycle of treatment, compared to baseline predicted both OS and PFS in R/M HNSCC patients on systemic therapy.

A decrease in ΔVAF identified patients with longer OS despite early radiological progression. Further prospective studies are needed to validate these findings.<br>

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Where it is published

Catalogue records · 1

Topics

Inferred from text
Cancer 75% · Immunology 70% · Longitudinal study 65% · Sequencing 75%
Provenance · 3 source records, 17 field assertions
SourceKeyLast seenRaw
ZivaHuboai:figshare.com:article/3280525710 d agoJSON v1
Deakin Research Onlineoai:figshare.com:article/3280525710 d agoJSON v1
DMU Figshareoai:figshare.com:article/3280525710 d agoJSON v1
FieldAssertionExtractorEvidence
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