Correction: Evaluation of ctDNA-guided adjuvant therapy de-escalation in head and neck squamous cell carcinoma: a comparative cohort study

Correction on: Zhang X, Fang Q, Yuan J, Dai L, Luo R, Huang T, Wu Y. Evaluation of ctDNA-guided adjuvant therapy de-escalation in head and neck squamous cell carcinoma: a comparative cohort study. Front Immunol. 2025;16:1576042. doi: 10.3389/fimmu.2025.1576042.Adding/removing text During re-checking the data in this manuscript, we find in the original publication, the methodology for the personalized, tumor-informed ctDNA testing was incorrectly stated as being performed "using the Signatera™ (Natera, Inc.) assay."A correction has been made to the section (ctDNA testing paragraph in Methods section, Page 3):This methodology aligns with previously published protocols (18). ctDNA was detected in plasma samples gathered prior to neoadjuvant chemoimmunotherapy and within 10-14 days postsurgery. Personalized, tumor-informed ctDNA testing was performed using Illumina (NextSeq 500/NovaSeq 6000) next-generation sequencing platform (Wanlei, Shenyang). Testing was conducted by our core facility, utilizing matched tumor tissue and blood samples to design patientspecific assays. Somatic mutations were identified via multiplex PCR amplification via a 16-plex PCR panel targeting tumor-derived variants, enabling bespoke detection with a sensitivity of 0.01% variant allele frequency. The bioinformatics pipeline included alignment (BWA-MEM), duplex consensus sequencing to reduce noise, and variant calling via a proprietary algorithm, with germline filtering using matched white blood cell-derived DNA. A plasma sample was classified as ctDNA-positive if ≥1 somatic variant was detected. Variant persistence in postoperative samples was confirmed if: the variant was detected pre-treatment, present in the binary comparison map file, or observed in ≥3 reads in postoperative plasma. ctDNA level was recorded with units of mean tumor molecules (MTM) per mL of plasma.

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Journal
Frontiers in Immunology
Published
2026-05-08
DOI
https://doi.org/10.3389/fimmu.2026.1845587
Primary Topic
Cancer Genomics and Diagnostics
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article
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article

Correction: Evaluation of ctDNA-guided adjuvant therapy de-escalation in head and neck squamous cell carcinoma: a comparative cohort study

Yinfei Wu, Liyuan Dai, Ruihua Luo, Qigen Fang et al.
Frontiers in Immunology
Cancer Genomics and Diagnostics
article

Correction: Evaluation of ctDNA-guided adjuvant therapy de-escalation in head and neck squamous cell carcinoma: a comparative cohort study

Yinfei Wu, Liyuan Dai, Ruihua Luo, Qigen Fang, Xu Zhang, Tao Huang, Junhui Yuan
article en

Abstract

Correction on: Zhang X, Fang Q, Yuan J, Dai L, Luo R, Huang T, Wu Y. Evaluation of ctDNA-guided adjuvant therapy de-escalation in head and neck squamous cell carcinoma: a comparative cohort study. Front Immunol. 2025;16:1576042. doi: 10.3389/fimmu.2025.1576042.Adding/removing text During re-checking the data in this manuscript, we find in the original publication, the methodology for the personalized, tumor-informed ctDNA testing was incorrectly stated as being performed "using the Signatera™ (Natera, Inc.) assay."A correction has been made to the section (ctDNA testing paragraph in Methods section, Page 3):This methodology aligns with previously published protocols (18). ctDNA was detected in plasma samples gathered prior to neoadjuvant chemoimmunotherapy and within 10-14 days postsurgery. Personalized, tumor-informed ctDNA testing was performed using Illumina (NextSeq 500/NovaSeq 6000) next-generation sequencing platform (Wanlei, Shenyang). Testing was conducted by our core facility, utilizing matched tumor tissue and blood samples to design patientspecific assays. Somatic mutations were identified via multiplex PCR amplification via a 16-plex PCR panel targeting tumor-derived variants, enabling bespoke detection with a sensitivity of 0.01% variant allele frequency. The bioinformatics pipeline included alignment (BWA-MEM), duplex consensus sequencing to reduce noise, and variant calling via a proprietary algorithm, with germline filtering using matched white blood cell-derived DNA. A plasma sample was classified as ctDNA-positive if ≥1 somatic variant was detected. Variant persistence in postoperative samples was confirmed if: the variant was detected pre-treatment, present in the binary comparison map file, or observed in ≥3 reads in postoperative plasma. ctDNA level was recorded with units of mean tumor molecules (MTM) per mL of plasma.

Frontiers in ImmunologyVol. 17
University of California San Diego (US), Zhengzhou University (CN), Henan Cancer Hospital (CN)
Good health and well-being
Openalex Percentile: Top 6%
Cancer Genomics and Diagnostics
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