Evidence map›Paper›PMID 40238760›Full record

ArticlePloS one2025

Evaluation of Onco E6 point of care rapid diagnostic test for human papilloma virus in Bahir Dar, Amhara Regional State, Ethiopia.

Alemayehu Abate, Abaineh Munshea, Endalkachew Nibret, Belay Bezabih, Bereket Amare, Gizachew Yismaw

Abstract readEvaluation Study
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

6 authors.

Alemayehu AbateHealth Biotechnology Division, Institute of Biotechnology, Bahir Dar University, Bahir Dar PO, Ethiopia.ORCID 0000-0003-4159-6288
Abaineh MunsheaHealth Biotechnology Division, Institute of Biotechnology, Bahir Dar University, Bahir Dar PO, Ethiopia.
Endalkachew NibretHealth Biotechnology Division, Institute of Biotechnology, Bahir Dar University, Bahir Dar PO, Ethiopia.
Belay BezabihAmhara Public Health Institute, Bahir Dar PO, Ethiopia.
Bereket AmareDepartment of Pathology, Afilas General Hospital, Bahir Dar, Ethiopia.
Gizachew YismawAmhara Public Health Institute, Bahir Dar PO, Ethiopia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCervical cancer is a malignant tumor arising from the cells of the uterine cervix. The oncogenic human papillomavirus (HPV) infection is the main causative agent of cervical cancer. Effective HPV screening program can lead to a significant reduction in the morbidity and mortality associated with this cancer.

objectiveThe aim of the study was to evaluate the diagnostic performance of OncoE6™ cervical test kit for cervical precancer and cancer in Amhara Regional State, northwest Ethiopia.

methodsAn institute-based cross-sectional study was conducted at Felege Hiwot Compressive Specialized Hospital which is found in Bahir Dar, Amhara Regional state. A total of 297 samples were collected. A sterile, disposable speculum was inserted, without lubricant, and two swabs were taken using the "Tipped Polyester" (Dacron) swab provided with the Onco E6™ kit. Swabs taken were tested for onco E6 proteins testing as per the manufacturer's protocol and pap smear for cytology test. A punch of biopsy was also taken for histopathological diagnosis. Data for all samples were collected using pre-prepared excel database for onco E6 test, pap cytology and punch histopathology. All the data were coded and entered into Epi-info and transported to SPSS version 26.0 software package for analysis.

resultsOut of 56 (18.86%) participants who tested positive on the histo-pathological diagnosis, Onco E6 was positive in 32 (57.14%), negative in 24 (42.85%). Of 241 participants who tested negative on the histo-pathological diagnosis, Onco E6 was positive in 5 (2.07%) and negative in 236 (97.9%). OncoE6™ cervical test kit had a sensitivity of 57.14% (95% CI: 43.22%-70.29%) and specificity of 98% (95% CI: 95.23%-99.32%) with positive predictive value of 86.6% (95% CI: 71.36%-95.53%), negative predictive value of 90.76% (95% CI: 86.49%-93.93%), and accuracy of 90.18% (95% CI: 86.21%-93.31%).

conclusionThe HPV 16/18 OncoE6™ Cervical test kit test had sub-optimum sensitivity and high specificity for detection of cervical precancer and cancer cases. The sensitivity of the kit could be increased by incorporating other more prevalent genotypes like genotype 52, 58, 31 and 35. The HPV16/18-E6 test could be used either as primary screening tool or in conjunction with other diagnostic methods.

Indexed as

Human papillomavirus 16Human papillomavirus 18Oncogene Proteins, ViralRapid Diagnostic TestsReagent Kits, DiagnosticRepressor ProteinsUterine Cervical NeoplasmsAdultCross-Sectional StudiesDNA-Binding ProteinsEthiopiaFemaleHumansMiddle AgedSensitivity and SpecificityVaginal SmearsDNA-Binding ProteinsE6 protein, Human papillomavirus type 16E6 protein, Human papillomavirus type 18Oncogene Proteins, ViralReagent Kits, DiagnosticRepressor Proteins

Identifiers

PMID40238760
PMCPMC12002466

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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.