Evidence map›Paper›PMID 36745662›Full record

ArticlePloS one2023

High sensitivity and specificity rates of cobas® HPV test as a primary screening test for cervical intraepithelial lesions in a real-world setting.

Laura Alicia Fleider, María de Los Ángeles Tinnirello, Facundo Gómez Cherey, María Gabriela García, Lucía Helena Cardinal, Florencia García Kamermann, Silvio Alejandro Tatti

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 14 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

7 authors at 1 institution in 1 country.

Laura Alicia FleiderOBGYN Department, Genital Tract Unit, Hospital de Clínicas "José de San Martín", Buenos Aires University, Buenos Aires, Argentina.ORCID 0000-0003-0871-2312
María de Los Ángeles TinnirelloOBGYN Department, Genital Tract Unit, Hospital de Clínicas "José de San Martín", Buenos Aires University, Buenos Aires, Argentina.
Facundo Gómez ChereyOBGYN Department, Genital Tract Unit, Hospital de Clínicas "José de San Martín", Buenos Aires University, Buenos Aires, Argentina.ORCID 0000-0003-0107-2834
María Gabriela GarcíaMolecular Infectious Disease Department, ManLab Laboratories, Buenos Aires, Argentina.ORCID 0000-0003-0571-6027
Lucía Helena CardinalGynecological Pathology Division, Pathology Department, Hospital de Clínicas "José de San Martín", Buenos Aires University, Buenos Aires, Argentina.
Florencia García KamermannGynecological Pathology Division, Pathology Department, Hospital de Clínicas "José de San Martín", Buenos Aires University, Buenos Aires, Argentina.
Silvio Alejandro TattiChief of OBGYN Department, Hospital de Clínicas "José de San Martín", Buenos Aires University, Buenos Aires, Argentina.
Hospital de Clínicas "José de San Martín" · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical carcinoma (CC) is the fourth most common malignancy among women. Screening with Papanicolau smear is linked to a reduction in CC incidence rates when screening programs have been developed. However, this technique has several limitations, including moderate sensitivity rates for detection of cervical preneoplastic HPV-related lesions. In this real-world study, we proposed to evaluate the sensitivity and specificity rates of cobas® test, which amplifies target DNA fragments by polymerase chain reaction and hybridization of nucleic acids for the detection of 14 HR-HPV types in a single analysis) used as primary screening test for CC and preneoplastic lesions in women aged 25-65 years in a large University Hospital in Buenos Aires. A total of 1044 patients were included in the sample (median age: 46 years); sensitivity and specificity rates for the HR-HPV test used as primary screening test were 98.66% (95% confidence interval [95CI]: 97.67-99.3%) and 87.15% (95CI: 84.93-89.15%), respectively. The positive predictive value was 88.47% (95CI: 86.54%-90.42%) and the negative predictive value was 98.48% (95CI: 97.75%-99.23%). The cobas® HR-HPV testing was highly sensitive and specific for the detection of CC and preneoplastic lesions in real practice.

Indexed as

CarcinomaPapillomavirus InfectionsUterine Cervical DysplasiaUterine Cervical NeoplasmsDNA, ViralEarly Detection of CancerFemaleHumansMass ScreeningMiddle AgedPapillomaviridaeSensitivity and SpecificityVaginal SmearsDNA, Viral

Identifiers

PMID36745662
PMCPMC9901754
OpenAlexW4319294329

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.