Evidence map›Paper›PMID 39913364›Full record

ArticleJournal of the National Cancer Institute2025

Impact of screening for human papillomavirus-positive oropharyngeal cancers: a microsimulation-based modeling study.

Rebecca Landy, Gregory W Haber, Barry I Graubard, Carole Fakhry, Nicole G Campos, Emily A Burger, Li C Cheung, Hormuzd A Katki, Maura L Gillison, Anil K Chaturvedi

Abstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Rebecca LandyDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD 20850, United States.ORCID 0000-0003-4042-4820
Gregory W HaberInformation Technology Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, United States.
Barry I GraubardDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD 20850, United States.ORCID 0000-0002-6787-1105
Carole FakhrySchool of Medicine, Johns Hopkins University, Baltimore, MD 21205, United States.ORCID 0000-0002-5251-6178
Nicole G CamposCenter for Health Decision Science, Harvard T. H. Chan School of Public Health, Boston, MA 02115, United States.ORCID 0000-0002-0840-4339
Emily A BurgerCenter for Health Decision Science, Harvard T. H. Chan School of Public Health, Boston, MA 02115, United States.ORCID 0000-0002-6657-5849
Li C CheungDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD 20850, United States.ORCID 0000-0003-1625-4331
Hormuzd A KatkiDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD 20850, United States.ORCID 0000-0003-2002-0095
Maura L GillisonMD Anderson Cancer Center, Houston, TX 77030, United States.
Anil K ChaturvediDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD 20850, United States.ORCID 0000-0003-2696-8899

Funding

Intramural Research ProgramNCI NIH HHSNIH HHS
6 · The paper itself

Abstract

backgroundWe estimated the impact of screening on morbidity and mortality of human papillomavirus (HPV)16-positive oropharyngeal cancer among US men aged 45-79 years.

methodsWe developed an individual-level, state-transition natural history microsimulation model to estimate the impact of screening using oral HPV16 detection, HPV16-E6 antibody detection, and transcervical ultrasound of neck/oropharynx. We compared clinical detection to counterfactual screen detection for cancer stage, single- vs multiple-modality treatment, and survival. Screening scenarios encompassed 4 progression speeds across cancer stages (very slow, slow, fast, and very fast) and 4 screening frequencies.

resultsAmong US men aged 45-79 years in 2021 (n = 54 881 311), 163 958 clinically diagnosed human papillomavirus (HPV)-positive oropharyngeal cancers and 32 009 deaths would occur through age 84 in the absence of screening. Assuming very-fast progression, 4%, 20%, 31%, and 60% of these cancers would be detected by one-off, 5-yearly, 3-yearly, and annual screening. Annual screening (very-fast progression) could reduce the number of cancers diagnosed at advanced stages (American Joint Committee on Cancer, 7th edition, stages III/IV: 90.0% with no screening vs 59.1%) and treated by multiple modalities (80.6% with no screening vs 50.6%). Cancer mortality would also be reduced by 36.2%, with a gain of 106 000 life-years. Annual screening would have a number needed to screen (NNS) of 561 per screen-detected cancer, 1118 per additional cancer treated by single modality, 4740 per death prevented, and 520 per life-year gained; such high NNS reflect potential inefficiency of population-level screening.

conclusionsIf proven efficacious in randomized trials and cost-effective, screening for HPV-positive oropharyngeal cancers could provide considerable population-level reductions in advanced stage cancers, treatment-related morbidities, and mortality.

Indexed as

Early Detection of CancerHuman papillomavirus 16Mass ScreeningOropharyngeal NeoplasmsPapillomavirus InfectionsAgedComputer SimulationDisease ProgressionHuman Papillomavirus VirusesHumansMaleMiddle AgedOncogene Proteins, ViralRepressor ProteinsUnited StatesE6 protein, Human papillomavirus type 16Oncogene Proteins, ViralRepressor Proteins

Identifiers

PMID39913364
PMCPMC12257938

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Registered trials

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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.