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dc.contributor.authorPham, Duc-Tien
dc.contributor.authorSkaland, Ivar
dc.contributor.authorWinther, Theo L.
dc.contributor.authorSalvesen, Øyvind
dc.contributor.authorTorp, Sverre Helge
dc.date.accessioned2021-09-20T07:27:46Z
dc.date.available2021-09-20T07:27:46Z
dc.date.created2019-11-27T07:46:30Z
dc.date.issued2019
dc.identifier.citationInternational Journal of Surgical Pathology. 2019, 1-7.en_US
dc.identifier.issn1066-8969
dc.identifier.urihttps://hdl.handle.net/11250/2779019
dc.description.abstractObjective. Proliferative activity in tumor tissues is assessed as the percentage of Ki-67/MIB-1-positive cells, or the proliferative index (PI). The PI is routinely assessed manually. However, the subjectivity of manual assessments might result in poor reproducibility. We hypothesized that digital assessments might reduce the error. Method. In our study, we assessed Ki-67/MIB-1 PIs, both manually and digitally, with tissue microarrays constructed from 141 human meningioma samples. Spearman-rank correlation and κ statistics were applied for correlation and agreement analyses, respectively. Mann-Whitney U tests were used to compare MIB-1 PIs between groups. Prognostic ability was assessed with Kaplan-Meier and Cox regression analyses. Results. We found a significant, high correlation (Spearman ρ = 0.832, P < .01) and moderate agreement (κ coefficient = 0.617, observed agreement = 80.9%) between the 2 methods. Both methods found significantly different Ki-67/MIB-1 PIs for different World Health Organization grades (P < .05). Neither method showed significant prognostic value. Conclusion. Digital determinations of Ki-67/MIB-1 PIs in human meningiomas are feasible for the daily routine.en_US
dc.language.isoengen_US
dc.publisherSAGEen_US
dc.titleCorrelation Between Digital and Manual Determinations of Ki-67/MIB-1 Proliferative Indices in Human Meningiomasen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-7en_US
dc.source.journalInternational Journal of Surgical Pathologyen_US
dc.identifier.doi10.1177/1066896919889148
dc.identifier.cristin1752826
dc.description.localcodeThis version of the article will not be available due to copyright restrictions (c) 2019 by SAGEen_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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