Identification of Atypical Circulating Tumor Cells with Prognostic Value in Metastatic Breast Cancer Patients. 2022

Alexia Lopresti, and Claire Acquaviva, and Laurys Boudin, and Pascal Finetti, and Séverine Garnier, and Anaïs Aulas, and Maria Lucia Liberatoscioli, and Olivier Cabaud, and Arnaud Guille, and Alexandre de Nonneville, and Quentin Da Costa, and Emilie Denicolai, and Jihane Pakradouni, and Anthony Goncalves, and Daniel Birnbaum, and François Bertucci, and Emilie Mamessier
Laboratory of Predictive Oncology, Cancer Research Center of Marseille, Inserm U1068-CNRS UMR7258-Université Aix-Marseille UM105, Label "Ligue Contre le Cancer", 13009 Marseille, France.

Circulating tumor cells have a strong potential as a quasi-non-invasive tool for setting up a precision medicine strategy for cancer patients. Using a second-generation "filtration-based" technology to isolate CTCs, the Screencell™ technology (Sarcelles, France), we performed a large and simultaneous analysis of all atypical circulating tumor cells (aCTCs) isolated from the blood of metastatic breast cancer (mBC) patients. We correlated their presence with clinicopathological and survival data. We included 91 mBC patients from the PERMED-01 study. The median number of aCTCs was 8.3 per mL of blood. Three subsets of aCTCs, absent from controls, were observed in patients: single (s-aCTCs), circulating tumor micro-emboli (CTM), and giant-aCTCs (g-aCTCs). The presence of g-aCTCs was associated with shorter progression free survival and overall survival. This study highlights the heterogeneity of aCTCs in mBC patients both at the cytomorphological and molecular levels. In addition, it suggests the usefulness of the g-aCTC subset as a prognostic factor and a potential stratification tool to treat late-stage mBC patients and improve their chances of benefiting from early clinical trials.

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