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dc.contributor.authorAbdo, M.*
dc.contributor.authorBelloum, Y.*
dc.contributor.authorHeigener, D.*
dc.contributor.authorWelker, L.*
dc.contributor.authorvon Weihe, S.*
dc.contributor.authorSchmidt, M.*
dc.contributor.authorHeuer-Olewinski, N.*
dc.contributor.authorWatermann, I.*
dc.contributor.authorSzewczyk, M.*
dc.contributor.authorKropidlowski, J.*
dc.contributor.authorPereira Veiga, Thais*
dc.contributor.authorElmas, H.*
dc.contributor.authorPerner, S.*
dc.contributor.authorSteurer, S.*
dc.contributor.authorWikman, H.*
dc.contributor.authorPantel, K.*
dc.contributor.authorReck, M.*
dc.date.accessioned2025-09-08T12:18:03Z
dc.date.available2025-09-08T12:18:03Z
dc.date.issued2023
dc.identifier.citationAbdo M, Belloum Y, Heigener D, Welker L, von Weihe S, Schmidt M, et al. Comparative evaluation of PD-L1 expression in cytology imprints, circulating tumour cells and tumour tissue in non-small cell lung cancer patients. Molecular Oncology. 2023;17(5):737-46.
dc.identifier.issn1878-0261
dc.identifier.otherhttps://portalcientifico.sergas.gal//documentos/6433d25fe8f2fa0e62f2b2d6
dc.identifier.urihttp://hdl.handle.net/20.500.11940/21247
dc.description.abstractAlternative sources of tumour information need to be explored in patients with non-small cell lung cancer (NSCLC). Here, we compared programmed cell death ligand 1 (PD-L1) expression on cytology imprints and circulating tumour cells (CTCs) with PD-L1 tumour proportion score (TPS) from immunohistochemistry staining of tumour tissue from patients with NSCLC. We evaluated PD-L1 expression using a PD-L1 antibody (28-8) in representative cytology imprints, and tissue samples from the same tumour. We report good agreement rates on PD-L1 positivity (TPS ? 1%) and high PD-L1 expression (TPS ? 50%). Considering high PD-L1 expression, cytology imprints showed a PPV of 64% and a NPV of 85%. CTCs were detected in 40% of the patients and 80% of them were PD-L1+. Seven patients with PD-L1 expression of < 1% in tissue samples or cytology imprints had PD-L1+ CTCs. The addition of PD-L1 expression in CTCs to cytology imprints markedly improved the prediction capacity for PD-L1 positivity. A combined analysis of cytological imprints and CTCs provides information on the tumoural PD-L1 status in NSCLC patients, which might be used when no tumor tissue is available.
dc.description.sponsorshipThis study was supported by an unrestricted research grant from Bristol Myers Squibb GmbH, Munich, Germany. YB and KP were financially supported by the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 765492.
dc.languageeng
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshHumans *
dc.subject.meshCarcinoma, Non-Small-Cell Lung *
dc.subject.meshLung Neoplasms *
dc.subject.meshB7-H1 Antigen*
dc.subject.meshNeoplastic Cells, Circulating*
dc.subject.meshImmunohistochemistry *
dc.subject.meshBiomarkers, Tumor*
dc.titleComparative evaluation of PD-L1 expression in cytology imprints, circulating tumour cells and tumour tissue in non-small cell lung cancer patients
dc.typeArtigo
dc.authorsophosAbdo, M.; Belloum, Y.; Heigener, D.; Welker, L.; von Weihe, S.; Schmidt, M.; Heuer-Olewinski, N.; Watermann, I.; Szewczyk, M.; Kropidlowski, J.; Pereira-Veiga, T.; Elmas, H.; Perner, S.; Steurer, S.; Wikman, H.; Pantel, K.; Reck, M.
dc.identifier.doi10.1002/1878-0261.13415
dc.identifier.sophos6433d25fe8f2fa0e62f2b2d6
dc.issue.number5
dc.journal.titleMolecular Oncology*
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS)::Oncoloxía médica
dc.page.initial737
dc.page.final746
dc.relation.projectIDBristol Myers Squibb GmbH, Munich, Germany
dc.relation.projectIDEuropean Union [765492]
dc.relation.publisherversionhttps://doi.org/10.1002/1878-0261.13415
dc.rights.accessRightsopenAccess*
dc.subject.keywordAS Santiago
dc.subject.keywordIDIS
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number17


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Attribution 4.0 International (CC BY 4.0)
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