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dc.contributor.authorNitschke, C.
dc.contributor.authorMarkmann, B.
dc.contributor.authorKonczalla, L.
dc.contributor.authorKropidlowski, J.
dc.contributor.authorPereira Veiga, Thais
dc.contributor.authorScognamiglio, P.
dc.contributor.authorSchönrock, M.
dc.contributor.authorSinn, M.
dc.contributor.authorTölle, M.
dc.contributor.authorIzbicki, J.
dc.contributor.authorPantel, K.
dc.contributor.authorUzunoglu, F.G.
dc.contributor.authorWikman, H.
dc.date.accessioned2025-08-26T11:02:39Z
dc.date.available2025-08-26T11:02:39Z
dc.date.issued2022
dc.identifier.citationNitschke C, Markmann B, Konczalla L, Kropidlowski J, Pereira-Veiga T, Scognamiglio P, et al. Circulating Cancer Associated Macrophage-like Cells as a Potential New Prognostic Marker in Pancreatic Ductal Adenocarcinoma. Biomedicines. 2022;10(11).
dc.identifier.issn2227-9059
dc.identifier.otherhttps://portalcientifico.sergas.gal/documentos/6416a5065db420433b7b62cf*
dc.identifier.urihttp://hdl.handle.net/20.500.11940/20832
dc.description.abstractBackground: Circulating Cancer Associated Macrophage-like cells (CAMLs) have been described as novel liquid biopsy analytes and unfavorable prognostic markers in some tumor entities, with scarce data for Pancreatic Ductal Adenocarcinomas (PDAC). Methods: Baseline and follow-up blood was drawn from resected curative (n = 36) and palliative (n = 19) PDAC patients. A microfluidic size-based cell enrichment approach (ParsortixTM) was used for CAML detection, followed by immunofluorescence staining using pan-keratin, CD14, and CD45 antibodies to differentiate between CAMLs, circulating tumor cells (CTCs), and leukocytes. Results: CAMLs were detectable at baseline in 36.1% of resected patients and 47.4% of palliative PDAC patients. CAML detection was tumor stage independent. Follow-up data indicated that detection of CAMLs (in 45.5% of curative patients) was an independent prognostic factor for shorter recurrence-free survival (RFS) (HR: 4.3, p = 0.023). Furthermore, a combined analysis with CTCs showed the detectability of at least one of these cell populations in 68.2% of resected patients at follow-up. The combined detection of CAMLs and CTCs was also significantly associated with short RFS (HR: 8.7, p = 0.003). Conclusions: This pilot study shows that detection of CAMLs in PDAC patients can provide prognostic information, either alone or even more pronounced in combination with CTCs, which indicates the power of liquid biopsy marker analyses.en
dc.description.sponsorshipWe thank Roggenbuck foundation (FGU, CN) for financial support, Deutsche Krebshilfe (CN) and Hamburger Krebsgesellschaft e.V. (BM) for funding scholarships covering personnel costs. We also thank the UKE foundation and Joachim Herz foundation for financial support.en
dc.language.isoeng
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleCirculating Cancer Associated Macrophage-like Cells as a Potential New Prognostic Marker in Pancreatic Ductal Adenocarcinoma*
dc.typeArticleen
dc.authorsophosNitschke, H. C.
dc.authorsophosMarkmann, B.
dc.authorsophosKonczalla, L.
dc.authorsophosKropidlowski, J.
dc.authorsophosPereira-Veiga, T.
dc.authorsophosScognamiglio, P.
dc.authorsophosSchönrock, M.
dc.authorsophosSinn, M.
dc.authorsophosTölle, M.
dc.authorsophosIzbicki, J.
dc.authorsophosPantel, K.
dc.authorsophosUzunoglu, F. G.
dc.authorsophosWikman
dc.identifier.doi10.3390/biomedicines10112955
dc.identifier.sophos6416a5065db420433b7b62cf
dc.issue.number11
dc.journal.titleBiomedicines*
dc.relation.projectIDRoggenbuck foundation; Deutsche Krebshilfe; Hamburger Krebsgesellschaft e.V.; UKE foundation; Joachim Herz foundation
dc.relation.publisherversionhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687633/pdf/biomedicines-10-02955.pdf;https://mdpi-res.com/d_attachment/biomedicines/biomedicines-10-02955/article_deploy/biomedicines-10-02955-v2.pdf?version=1668767191es
dc.rights.accessRightsopenAccess
dc.subject.keywordAS Santiagoes
dc.subject.keywordIDISes
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number10


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