Evidence map›Paper›PMID 27501394›Full record

ArticleCancer science2016

Comparison of methods using paraffin-embedded tissues and exfoliated cervical cells to evaluate human papillomavirus genotype attribution.

Yutaka Torii, Takuma Fujii, Iwao Kukimoto, Miyuki Saito, Takashi Iwata, Hiroshi Takahashi, Ryoko Ichikawa, Satoshi Kawai, Sayaka Otani, Daisuke Aoki

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 8 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

10 authors at 3 institutions in 1 country.

Yutaka ToriiDepartment of Obstetrics and Gynecology, School of Medicine, Fujita Health University, Toyoake, Japan.
Takuma FujiiDepartment of Obstetrics and Gynecology, School of Medicine, Fujita Health University, Toyoake, Japan. fujiit44@fujita-hu.ac.jp.
Iwao KukimotoPathogen Genomics Center, National Institute of Infectious Diseases, Tokyo, Japan.
Miyuki SaitoDepartment of Obstetrics and Gynecology, School of Medicine, Keio University, Tokyo, Japan.
Takashi IwataDepartment of Obstetrics and Gynecology, School of Medicine, Keio University, Tokyo, Japan.
Hiroshi TakahashiDivision of Medical Statistics, School of Medicine, Fujita Health University, Toyoake, Japan.
Ryoko IchikawaDepartment of Obstetrics and Gynecology, School of Medicine, Fujita Health University, Toyoake, Japan.
Satoshi KawaiDepartment of Obstetrics and Gynecology, School of Medicine, Fujita Health University, Toyoake, Japan.
Sayaka OtaniDepartment of Obstetrics and Gynecology, School of Medicine, Fujita Health University, Toyoake, Japan.
Daisuke AokiDepartment of Obstetrics and Gynecology, School of Medicine, Keio University, Tokyo, Japan.
Fujita Health University · JPKeio University · JPNational Institute of Infectious Diseases · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monitoring the attribution of human papillomavirus (HPV) genotypes to cervical precancerous lesions is essential in assessing the efficacy of HPV vaccines. To resolve the lack of studies comparing the HPV genotyping procedures used to estimate HPV genotype attribution, we undertook a retrospective cross-sectional study to determine the appropriate genotyping procedures for evaluating the potential efficacy of HPV vaccines. Three procedures, including two different genotyping methods, Clinichip HPV test (C-Chip) and modified GP5+/6+ PCR coupled to fluorescent bead sorter detection (MGP), using exfoliated cervical cells (C-Chip and C-MGP, respectively) or formalin-fixed paraffin-embedded tissues (F-MGP), were compared. The overall agreement in detecting high-risk HPV was 88.5-92.1% among the three procedures, and genotype-specific agreement was 83.9-100% for all pairwise comparisons. In cervical intraepithelial neoplasia grade 2/3 specimens, HPV16/18 attribution estimated with the hierarchical attribution method was consistent among the procedures: 52.3% (45/86) for C-Chip, 54.7% (47/86) for C-MGP, and 52.3% (45/86) for F-MGP (P = 0.81). HPV16/18/31/33/45/52/58 hierarchical attribution was 88.4% (76/86) with C-Chip, 86.0% (74/86) with C-MGP, and 83.7% (72/86) with F-MGP (P = 0.49). In cervical intraepithelial neoplasia grade 3 specimens, the corresponding hierarchical attribution was 96.4% (53/55) with C-Chip, 89.1% (49/55) with C-MGP, and 94.5% (52/55) with F-MGP (P = 0.27). Although F-MGP is theoretically a reliable method for determining HPV genotype attribution, it is acceptable to use C-Chip or C-MGP, coupled to the hierarchical attribution formula to correct the bias of multiple infections. These approaches using exfoliated cervical cells are practical for monitoring the efficacy of HPV vaccines.

Indexed as

GenotypeAdultCervix UteriCross-Sectional StudiesDNA, ViralFemaleGenotyping TechniquesHumansMiddle AgedNeoplasm GradingPapillomaviridaePapillomavirus InfectionsPapillomavirus VaccinesUterine Cervical DysplasiaYoung AdultDNA, ViralPapillomavirus VaccinesCervical intraepithelial neoplasiaexfoliated cervical cellformalin-fixed paraffin-embedded tissueHPV vaccinehuman papillomavirus

Identifiers

PMID27501394
PMCPMC5084667
OpenAlexW2522623228

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.