Evidence map›Paper›PMID 41979363›Full record

ArticleOtolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery2026

Nanopore Sequencing for HPV in Oropharyngeal Squamous Cell Carcinoma and Benign Tonsil Specimens.

Mikayla G Hubbard, Guang-Sheng Lei, Robert Emerson, Danielle Schreiber, Thomas E Davis, Diane W Chen

Abstract read
In one paragraph

Article in Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Mikayla G HubbardDepartment of Otolaryngology-Head and Neck Surgery, Indiana University School of Medicine, Indianapolis, Indiana, USA.ORCID https://orcid.org/0009-0001-3644-6800
Guang-Sheng LeiDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Robert EmersonDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Danielle SchreiberDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Thomas E DavisDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Diane W ChenDepartment of Otolaryngology-Head and Neck Surgery, Indiana University School of Medicine, Indianapolis, Indiana, USA.ORCID https://orcid.org/0000-0003-1809-7819

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesHuman papillomavirus (HPV) accounts for the majority of oropharyngeal squamous cell carcinoma (OPSCC) cases in the United States but understanding the prevalence of high-risk HPV in oropharyngeal tissue remains poor. We evaluated nanopore sequencing, a novel rapid, and long-read sequencing platform, on OPSCC tissue and tested it in benign tonsils from pediatric and young adult patients. STUDY

designCross-sectional study.

settingAcademic tertiary referral center.

methodsFormalin-fixed, paraffin-embedded (FFPE) specimens of HPV-positive and negative OPSCC diagnosed from 2013 to 2023 were sequenced on the nanopore MinION platform using an amplicon-based approach. Nanopore sequencing was subsequently performed on FFPE tissue from benign tonsillectomy in patients ages 30 and younger performed from 2016 to 2023.

resultsIn 54 OPSCC cases, nanopore sequencing detected HPV DNA in all 27 HPV-positive specimens with 96% of cases exhibiting high abundance (HPV reads >1000). HPV DNA was also detectable in all 27 HPV-negative specimens, but 89% had a low abundance. By interpreting high HPV abundance as HPV-positive, nanopore sequencing demonstrated a 96% sensitivity, 89% specificity, 90% positive predictive value, and 96% negative predictive value rate. In 150 benign tonsillectomy cases, 27% had HPV DNA detected by nanopore sequencing, all in low abundance, including 37% of patients younger than 10 years old. HPV DNA sequences detected belonged to subtype 16.

conclusionsNanopore sequencing demonstrated high sensitivity and specificity for HPV DNA in FFPE OPSCC tissue. High-risk HPV prevalence in pediatric and young adults may be higher than previously studied.

Indexed as

Carcinoma, Squamous CellHuman Papillomavirus VirusesNanopore SequencingOropharyngeal NeoplasmsPalatine TonsilPapillomavirus InfectionsAdolescentAdultChildCross-Sectional StudiesDNA, ViralFemaleHumansMaleYoung AdultDNA, Viralhuman papillomavirusnanopore sequencingoropharyngeal squamous cell carcinoma

Identifiers

PMID41979363
PMCPMC13327439

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.