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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dk.um.si/IzpisGradiva.php?id=88403"><dc:title>Association of circulating tumor cells, megakaryocytes and a high immune-inflammatory environment in metastatic breast cancer</dc:title><dc:creator>Grašič-Kuhar,	Cvetka	(Avtor)
	</dc:creator><dc:creator>Jernej,	Silvester	(Avtor)
	</dc:creator><dc:creator>Mencinger,	Marina	(Avtor)
	</dc:creator><dc:creator>Ovčariček,	Tanja	(Avtor)
	</dc:creator><dc:creator>Čemažar,	Maja	(Avtor)
	</dc:creator><dc:creator>Miceska,	Simona	(Avtor)
	</dc:creator><dc:creator>Modic,	Živa	(Avtor)
	</dc:creator><dc:creator>Kuhar,	Anamarija	(Avtor)
	</dc:creator><dc:creator>Jesenko,	Tanja	(Avtor)
	</dc:creator><dc:creator>Kloboves-Prevodnik,	Veronika	(Avtor)
	</dc:creator><dc:subject>breast cancer</dc:subject><dc:subject>circulating tumor cell</dc:subject><dc:subject>cluster</dc:subject><dc:subject>megakaryocyte</dc:subject><dc:subject>pan-inflammatory value</dc:subject><dc:subject>overall survival</dc:subject><dc:description>Liquid biopsy is becoming an important source of new biomarkers during the treatment of metastatic cancer patients. Using size-based microfluid technology, we isolated circulating tumor cells (CTCs) from metastatic breast cancer patients to evaluate their presence and cluster formation, as well as the presence of megakaryocytes and immune-inflammatory blood cells, and to correlate their presence with clinicopathological data and overall survival (OS). In total, 59 patients (median age 60.4 years) were included in the study: 62.7% luminal A/B-like, 20.3% HER2-positive, and 17% triple-negative. Our results showed that at least one CTC was present in 79.7% and ≥5 CTCs in 35.2% of the patients. CTC clusters were present in patients with ≥5 CTCs only (in 19.2% of them), and megakaryocytes were present in 52% of all patients. The presence of CTC clusters and megakaryocytes was positively associated with the CTC count. Patients with low pan-inflammatory value (PIV), low systemic immune-inflammatory index (SII), and low relative change from baseline (ΔPIV%, ΔSII%) were associated with significantly higher OS than their counterparts. ΔPIV%, the presence of infection in the last month, and a long duration of metastatic disease were identified as independent prognostic factors for OS. The interplay of CTCs, CTC clusters, megakaryocytes, and PIV needs to be further explored.</dc:description><dc:publisher>MDPI</dc:publisher><dc:date>2023</dc:date><dc:date>2024-04-19 13:02:56</dc:date><dc:type>Znanstveno delo</dc:type><dc:identifier>88403</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
