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Circulating Tumor Cell Kinetics and Morphology from the Liquid Biopsy Predict Disease Progression in Patients with Metastatic Colorectal Cancer Following Resection

Authors :
Drahomír Kolenčík
Sachin Narayan
Jana-Aletta Thiele
Dillon McKinley
Anna Sandström Gerdtsson
Lisa Welter
Petr Hošek
Pavel Ostašov
Ondřej Vyčítal
Jan Brůha
Ondřej Fiala
Ondřej Šorejs
Václav Liška
Pavel Pitule
Peter Kuhn
Stephanie N. Shishido
Source :
Cancers; Volume 14; Issue 3; Pages: 642, Cancers, Vol 14, Iss 642, p 642 (2022)
Publication Year :
2022
Publisher :
Multidisciplinary Digital Publishing Institute, 2022.

Abstract

The liquid biopsy has the potential to improve current clinical practice in oncology by providing real-time personalized information about a patient’s disease status and response to treatment. In this study, we evaluated 161 peripheral blood (PB) samples that were collected around surgical resection from 47 metastatic colorectal cancer (mCRC) patients using the High-Definition Single Cell Assay (HDSCA) workflow. In conjunction with the standard circulating tumor cell (CTC) enumeration, cellular morphology and kinetics between time-points of collection were considered in the survival analysis. CTCs, CTC-Apoptotic, and CTC clusters were found to indicate poor survival with an increase in cell count from pre-resection to post-resection. This study demonstrates that CTC subcategorization based on morphological differences leads to nuanced results between the subtypes, emphasizing the heterogeneity within the CTC classification. Furthermore, we show that factoring in the time-point of each blood collection is critical, both for its static enumeration and for the change in cell populations between draws. By integrating morphology and time-based analysis alongside standard CTC enumeration, liquid biopsy platforms can provide greater insight into the pathophysiology of mCRC by highlighting the complexity of the disease across a patient’s treatment.

Details

Language :
English
ISSN :
20726694
Database :
OpenAIRE
Journal :
Cancers; Volume 14; Issue 3; Pages: 642
Accession number :
edsair.doi.dedup.....d341873b6b50f3c225d842b96e16e702
Full Text :
https://doi.org/10.3390/cancers14030642