Evidence map›Paper›PMID 35640960›Full record

Observational studyBMJ (Clinical research ed.)2022

Extension of cervical screening intervals with primary human papillomavirus testing: observational study of English screening pilot data.

Matejka Rebolj, Kate Cuschieri, Christopher S Mathews, Francesca Pesola, Karin Denton, Henry Kitchener, HPV pilot steering group

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in BMJ (Clinical research ed.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 3 pooled it
6.4field-weighted citation impact, top 2% 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.

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

26 citing papers in PubMed, 3 syntheses or guidelines pooled it, 45 citations in OpenAlex.

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  11. Implementation of second round of HPV-based screening for cervical cancer in programmatic contexts in Argentina.Revista panamericana de salud publica = Pan American journal of public health · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Matejka ReboljCancer Prevention Group, School of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK matejka.rebolj@kcl.ac.uk.ORCID 0000-0001-9597-645X
Kate CuschieriScottish HPV Reference Laboratory, Royal Infirmary of Edinburgh, NHS Lothian Scotland, Edinburgh, UK.ORCID 0000-0002-2604-3928
Christopher S MathewsCancer Prevention Group, School of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.ORCID 0000-0002-3653-1810
Francesca PesolaCancer Prevention Group, School of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.ORCID 0000-0002-2054-7930
Karin DentonSevern Pathology, Southmead Hospital, North Bristol NHS Trust, Bristol, UK.ORCID 0000-0001-6957-895X
Henry KitchenerDivision of Cancer Sciences, University of Manchester, Manchester, UK.ORCID 0000-0001-5791-7838
HPV pilot steering group
King's College London · GBNHS Lothian · GBNorth Bristol NHS Trust · GBUniversity of Manchester · GB

Funding

Cancer Research UK 27047
6 · The paper itself

Abstract

objectivesTo provide updated evidence about the risk of cervical intraepithelial neoplasia grade 3 or higher (CIN3+) and cervical cancer after a negative human papillomavirus (HPV) test in primary cervical screening, by age group and test assay.

designObservational study.

settingReal world data from the English HPV screening pilot's first and second rounds (2013-16, follow-up to end of 2019).

participants1 341 584 women.

interventionsCervical screening with HPV testing or liquid based cytological testing (cytology or smear tests). Women screened with cytology were referred to colposcopy after high grade cytological abnormalities or after borderline or low grade abnormalities combined with a positive HPV triage test. Women screened with HPV testing who were positive were referred at baseline if their cytology triage test showed at least borderline abnormalities or after a retest (early recall) at 12 and 24 months if they had persistent abnormalities.

main outcome measuresDetection of CIN3+ and cervical cancer after a negative HPV test.

resultsFor women younger than 50 years, second round detection of CIN3+ in this study was significantly lower after a negative HPV screen in the first round than after cytology testing (1.21/1000

conclusionsThese data support an extension of the screening intervals, regardless of the test assay used: to five years after a negative HPV test in women aged 25-49 years, and even longer for women aged 50 years and older. The screening interval for HPV positive women who have negative HPV tests at early recall should be kept at three years.

Indexed as

AlphapapillomavirusPapillomavirus InfectionsUterine Cervical DysplasiaUterine Cervical NeoplasmsAgedEarly Detection of CancerFemaleHumansMiddle AgedPapillomaviridaeVaginal Smears

Identifiers

PMID35640960
PMCPMC9153243
OpenAlexW4281864550

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.