Evidence map›Paper›PMID 28498639›Full record

ArticleCancer cytopathology2017

Three-year risk of high-grade CIN for women aged 30 years or older who undergo baseline Pap cytology and HPV co-screening.

Ming Guo, Abha Khanna, Jianping Wang, Marilyn A Dawlett, Teresa L Kologinczak, Genevieve R Lyons, Roland L Bassett, Nour Sneige, Yun Gong, Therese B Bevers

Abstract read
In one paragraph

Article in Cancer cytopathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Observational
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.

Ming GuoDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID http://orcid.org/0000-0002-6773-1145
Abha KhannaDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jianping WangDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Marilyn A DawlettDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Teresa L KologinczakDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Genevieve R LyonsDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Roland L BassettDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Nour SneigeDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Yun GongDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Therese B BeversCancer Prevention Center, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

backgroundPapanicolaou (Pap) cytology and high-risk human papillomavirus (HPV) DNA cotesting for women aged ≥30 years are recommended for the prevention of cervical cancer. The objective of the current study was to evaluate the efficacy of this cotesting for predicting the risk of high-grade cervical intraepithelial neoplasia 3 (CIN3) during a 3-year follow-up period.

methodsA retrospective database search identified women aged ≥30 years who had baseline HPV and Pap cytology cotesting results in 2007 or 2008 and for whom 3-year follow-up results were available. The cumulative 3-year risks of developing CIN-3 were calculated.

resultsThe 3-year follow-up data after baseline Pap/HPV cotesting were available for 1986 women (mean age, 53 years). Of the 1668 women who had a baseline Pap-negative (Pap-)/HPV- cotesting result, 1561 (93.6%) had a follow-up Pap cytology result that was negative for intraepithelial lesions or malignancy. Of the 1530 women who had follow-up Pap/HPV cotesting, 1504 (98.3%) had a Pap-/HPV- result. The 3-year cumulative risk of developing CIN-3 was found to be highest for women with a baseline Pap-positive (Pap+)/HPV+ cotesting result (12.5%); the risk of CIN-3 was lower in those with a Pap-/HPV+ result (1.5%; P = .0032) or a Pap-/HPV- result (0.06%; P<.0001). The 3-year cumulative risk of CIN-3 was found to be significantly greater for women with an HPV+ result (4.8%) compared with those with an HPV- result (0.06%; P<.0001).

conclusionsPap cytology and HPV cotesting are valuable for stratifying CIN-3 risk. Pap cytology and HPV co-screening at a 3-year screening interval appears to carry a low risk of CIN-3 for women who have a baseline Pap-/HPV- cotesting result. Cancer Cytopathol 2017;125:644-51. © 2017 American Cancer Society.

Indexed as

AdultAgedAtypical Squamous Cells of the CervixDatabases, FactualEarly Detection of CancerFemaleHuman Papillomavirus DNA TestsHumansMiddle AgedNeoplasm GradingPapanicolaou TestPapillomavirus InfectionsRetrospective StudiesRisk AssessmentSquamous Intraepithelial Lesions of the CervixUterine Cervical Dysplasiacancer screening testscervical intraepithelial neoplasia (CIN)follow-up studieshuman papillomavirus (HPV)Papanicolaou (Pap) test

Identifiers

PMID28498639
PMCPMC5555795

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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.