Evidence map›Paper›PMID 32990181›Full record

ArticleHuman vaccines & immunotherapeutics2021

Human papillomavirus genotype-specific risks for cervical intraepithelial lesions.

Mari Nygård, Bo T Hansen, Susanne K Kjaer, Maria Hortlund, Laufey Tryggvadóttir, Christian Munk, Camilla Lagheden, Lara G Sigurdardottir, Suzanne Campbell, Kai-Li Liaw and 1 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01077856 (GARDASIL™ Vaccine Impact in Population Study), which is not on this map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.2field-weighted citation impact, top 7% of its field
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.

NCT01077856 completednot on this map

GARDASIL™ Vaccine Impact in Population Study

TypeobservationalSponsorMerck Sharp & Dohme LLCRan2007 to 2014Enrolled54,516ConditionsHuman Papillomavirus Infections
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 38 citations in OpenAlex.

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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

11 authors at 7 institutions in 5 countries.

Mari NygårdDepartment of Research, Cancer Registry of Norway, Oslo, Norway.
Bo T HansenDepartment of Research, Cancer Registry of Norway, Oslo, Norway.
Susanne K KjaerVirus, Lifestyle and Genes, Danish Cancer Society Research Center, Copenhagen, Denmark.
Maria HortlundFormerly at WHO HPV LabNet Global Reference Laboratory, Clinical Microbiology, Skåne University Hospital, Malmö, Sweden.ORCID 0000-0002-2627-4451
Laufey TryggvadóttirIcelandic Cancer Registry, Icelandic Cancer Society, Reykjavik, Iceland.
Christian MunkVirus, Lifestyle and Genes, Danish Cancer Society Research Center, Copenhagen, Denmark.
Camilla LaghedenFormerly at WHO HPV LabNet Global Reference Laboratory, Clinical Microbiology, Skåne University Hospital, Malmö, Sweden.
Lara G SigurdardottirIcelandic Cancer Registry, Icelandic Cancer Society, Reykjavik, Iceland.
Suzanne CampbellDepartment of Research, Cancer Registry of Norway, Oslo, Norway.ORCID 0000-0003-0818-9752
Kai-Li LiawMerck Research Laboratories, Merck Sharp & Dohme, Kenilworth, NJ, USA.
Joakim DillnerFormerly at WHO HPV LabNet Global Reference Laboratory, Clinical Microbiology, Skåne University Hospital, Malmö, Sweden.
Cancer Registry of Norway · NOKarolinska Institutet · SECopenhagen University Hospital · DKDanish Cancer Society · DKIcelandic Cancer Society · ISMerck & Co., Inc., Rahway, NJ, USA (United States) · USUniversity of Iceland · IS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prevalence of different HPV genotypes is changing after HPV vaccination. The associated risks are needed for optimizing cervical cancer screening.To estimate HPV type-specific prevalence, odds ratio (OR), and positive predictive value (PPV) for cervical cytological abnormalities, we determined 41 different HPV genotypes in cervical samples from a population-based sample of 8351 women aged 18-51 years before HPV vaccination era (V501-033; NCT01077856).Prevalence of HPV16 was 4.9% (95% CI: 4.4-5.5) with the PPV for high-grade cytology 11.2%, and OR 11.9 (95% CI: 8.5-16.5). Carcinogenic HPVs included in the nonavalent vaccine (HPV16,18,31,33,45,52,58) had a population prevalence of 14.4% (95% CI: 13.5-15.4), with PPV of 8.0% (95% CI: 6.8-9.3) and OR 23.7 (95% CI: 16.0-63.5) for high-grade cytology. HPV types currently included in most screening tests, but not vaccinated against (HPV35,39,51,56,59,66,68) had a joint prevalence of 8.5% (95% CI: 7.8-9.2) with PPV of 4.4% (95% CI: 3.3-5.7) and OR of 2.9 (95% CI: 2.0-4.0) for high-grade cytology. The other 27 non-carcinogenic genotypes had a prevalence of 11.8%, PPV of 2.9% (95% CI:2.1-3.9), and OR 1.5 (95% CI: 1.1-2.2.) for high-grade cytology.These results suggest that HPV screening tests in the post-vaccination era might perform better if restricted to the HPV types in the nonavalent vaccine and screening for all 14 HPV types might result in suboptimal balance of harms and benefits.

Indexed as

Papillomavirus InfectionsUterine Cervical DysplasiaUterine Cervical NeoplasmsEarly Detection of CancerFemaleGenotypeHuman papillomavirus 16HumansPapillomaviridaeDenmarkhigh-risk HPVIcelandliquid-based cytologylow-risk HPVNorwaypopulation-based prevalenceSweden

Identifiers

PMID32990181
PMCPMC8018444
OpenAlexW3089984332

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.