Evidence map›Paper›PMID 24557438›Full record

Trial reportInternational journal of gynecological cancer : official journal of the International Gynecological Cancer Society2014

A multicountry evaluation of careHPV testing, visual inspection with acetic acid, and papanicolaou testing for the detection of cervical cancer.

Jose Jeronimo, Pooja Bansil, Jeanette Lim, Roger Peck, Proma Paul, Juan Jose Amador, Florence Mirembe, Josaphat Byamugisha, Usha Rani Poli, Labani Satyanarayana and 2 more

Open access · bronzeAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in International journal of gynecological cancer : official journal of the International Gynecological Cancer Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed, 8 pooled it
13.9field-weighted citation impact, top 1% 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

99 citing papers in PubMed, 8 syntheses or guidelines pooled it, 175 citations in OpenAlex.

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39 more citing papers are in PubMed but not listed here.

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

12 authors at 6 institutions in 3 countries.

Jose Jeronimo*Program for Appropriate Technology in Health (PATH), Reproductive Health Global Program, Seattle, WA; †PATH, Reproductive Health Program, Kampala, Uganda; ‡Department of Obstetrics and Gynecology, Makerere University, Kampala, Uganda; §Department of Obstetrics and Gynecology, Mulago Hospital, Kampala, Uganda; ∥MNJ Cancer Institute, Oncology and Regional Cancer Center, Hyderabad, India; and ¶Institute of Cytology and Preventive Oncology, Uttar Pradesh, India.
Pooja Bansil
Jeanette Lim
Roger Peck
Proma Paul
Juan Jose Amador
Florence Mirembe
Josaphat Byamugisha
Usha Rani Poli
Labani Satyanarayana
Smita Asthana
START-UP Study Group
Program for Appropriate Technology in Health · INCancer Institute (WIA) · INMakerere University · UGMulago Hospital · UGProgram for Appropriate Technology in Health · USWorld Health Organization - Uganda · UG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study evaluates the feasibility and performance of careHPV, a novel human papillomavirus (HPV) DNA test, when used for screening women for cervical cancer in low-resource settings. METHODS AND MATERIALS: Clinician-collected (cervical) and self-collected (vaginal) careHPV specimens, visual inspection with acetic acid (VIA), and Papanicolaou test were evaluated among 16,951 eligible women in India, Nicaragua, and Uganda. Women with positive screening results received colposcopy and histologic follow-up as indicated. The positivity of each screening method was calculated overall, by site, and age. In addition, the clinical performance of each screening test was determined for detection of cervical intraepithelial neoplasia (CIN) grade 2 (CIN2+) and CIN grade 3.

resultsModerate or severe dysplasia or cancer (taken together as CIN2+) was diagnosed in 286 women. The positivity rate ranged between 2.4% to 19.6% for vaginal careHPV, 2.9% to 20.2% for cervical careHPV, 5.5% to 34.4% for VIA, and 2.8% to 51.8% for Papanicolaou test. Cervical careHPV was the most sensitive for CIN2+ (81.5%; 95% confidence interval [CI], 76.5-85.8) and CIN grade 3 (85.3%; 95% CI, 78.6-90.6) at all sites, followed by vaginal careHPV (69.6% and 71.3%, respectively). The sensitivity of VIA ranged from 21.9% to 73.6% and Papanicolaou test from 40.7% to 73.7%. The pooled specificities of cervical careHPV, vaginal careHPV, VIA, and Papanicolaou test were 91.6%, 90.6%, 84.2%, and 87.7%, respectively.

conclusionscareHPV performed well in large multicountry demonstration studies conducted in resource-limited settings that have not previously been conducted this type of testing; its sensitivity using cervical samples or vaginal self-collected samples was better than VIA or Papanicolaou test. The feasibility of using careHPV in self-collected vaginal samples opens the possibility of increasing coverage and early detection in resource-constrained areas.

Indexed as

Acetic AcidAdultAlphapapillomavirusDeveloping CountriesDNA, ViralFeasibility StudiesFemaleHumansPapanicolaou TestUterine Cervical DysplasiaUterine Cervical NeoplasmsVaginal SmearsAcetic AcidDNA, Viral

Identifiers

PMID24557438
PMCPMC4047307
OpenAlexW1987105544

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.