PD-L1 assessment in needle core biopsies of non-small cell lung cancer: Interpathologist agreement and potential associated histopathological features

dc.authorid0000-0001-7036-9813
dc.contributor.authorHacıhasanoğlu, Ezgi
dc.contributor.authorBambul Sığırcı, Buket
dc.contributor.authorUsul, Gamze
dc.contributor.authorŞavlı, Taha Cumhan
dc.date.accessioned2024-02-23T12:53:24Z
dc.date.available2024-02-23T12:53:24Z
dc.date.issued2024
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Tıbbi Patoloji Ana Bilim Dalı
dc.description.abstractObjective: Immune checkpoint inhibitors are used in the treatment of non -small cell lung cancer (NSCLC). Programmed cell death-ligand 1 (PD -L1) immunohistochemistry (IHC) assessed by pathologists is subject to interobserver variability. In advanced/metastatic disease and inoperable patients, PD -L1 assessment relies on biopsy specimens, commonly needle core biopsies (NCB). We aimed to determine the interobserver agreement for PD -L1 tumor proportion score (TPS) in NSCLC NCBs and identify histopathological features that may be related to interobserver variability. Material and Methods: Sixty NSCLC NCBs with PD -L1 IHC were evaluated independently by four pathologists from different institutions. PD -L1 TPS was evaluated in three categories: no/low expression (<1%), intermediate expression (1%-49%), and high expression (>= 50%). Histological tumor type, necrosis, tumor -infiltrating lymphocytes, tumor length/percentage in the biopsy, and crush/squeeze artifact was evaluated. Results: The statistical analysis of the three PD -L1 TPS categories demonstrated moderate agreement (Fleiss Kappa 0.477) in the no/low category, fair agreement (Fleiss Kappa 0.390) in the intermediate category, and almost perfect agreement (Fleiss Kappa 0.952) in the high category. A significant correlation (p=0.003) was found between the crush/squeeze artifact in NCB and rate of discordant TPS categories. There was no significant correlation between pathologists' agreement in the TPS categories and histological tumor type, tumor length, tumor ratio, necrosis, and tumor -infiltrating lymphocytes. Conclusion: Our results demonstrated moderate agreement among pathologists for the PD -L1 TPS 1% cut-off in NSCLC NCB, which is lower than that reported in resection materials. The presence of crush/squeeze artifact in NCBs is significantly related to the rate of discordant TPS categories, suggesting that PD -L1 assessment of pulmonary NCBs requires an awareness of this artifact.
dc.identifier.citationHacıhasanoğlu, E., Bambul Sığırcı, B., Usul, G. ve Şavlı, T. C. (2024). PD-L1 assessment in needle core biopsies of non-small cell lung cancer: Interpathologist agreement and potential associated histopathological features. Turkish Journal of Pathology, 40(1), 37-44. https://dx.doi.org/10.5146/tjpath.2023.01609
dc.identifier.doi10.5146/tjpath.2023.01609
dc.identifier.endpage44
dc.identifier.issn1018-5615
dc.identifier.issn1309-5730
dc.identifier.issue1
dc.identifier.pmid37614090
dc.identifier.scopusqualityN/A
dc.identifier.startpage37
dc.identifier.urihttps://dx.doi.org/10.5146/tjpath.2023.01609
dc.identifier.urihttps://hdl.handle.net/20.500.12511/12312
dc.identifier.volume40
dc.identifier.wos001157776000004en_US
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorŞavlı, Taha Cumhan
dc.language.isoen
dc.publisherFederation of Turkish Pathology Societies
dc.relation.ispartofTurkish Journal of Pathologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectProgrammed Death Ligand 1
dc.subjectLung
dc.subjectInterobserver
dc.subjectBiopsy
dc.subjectNeedle
dc.titlePD-L1 assessment in needle core biopsies of non-small cell lung cancer: Interpathologist agreement and potential associated histopathological features
dc.typeArticle

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