Association of Circulating Tumor Cells, Megakaryocytes and a High Immune-Inflammatory Environment in Metastatic Breast Cancer

Author:

Grašič Kuhar Cvetka12ORCID,Silvester Jernej2,Mencinger Marina1,Ovčariček Tanja1,Čemažar Maja34ORCID,Miceska Simona25,Modic Živa23ORCID,Kuhar Anamarija5,Jesenko Tanja23ORCID,Kloboves Prevodnik Veronika56ORCID

Affiliation:

1. Department Medical Oncology, Institute of Oncology, 1000 Ljubljana, Slovenia

2. Faculty of Medicine Ljubljana, University of Ljubljana, 1000 Ljubljana, Slovenia

3. Department of Experimental Oncology, Institute of Oncology, 1000 Ljubljana, Slovenia

4. Faculty of Health Sciences, University of Primorska, 6000 Izola, Slovenia

5. Department of Cytopathology, Institute of Oncology, 1000 Ljubljana, Slovenia

6. Faculty of Medicine, University of Maribor, 2000 Ljubljana, Slovenia

Abstract

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.

Funder

Slovenian Research Agency

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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