Circulating Polyploid Giant Cancer Cells, a Potential Prognostic Marker in Patients with Carcinoma

Author:

Chinen Ludmilla Thomé Domingos12,Torres Jacqueline Aparecida3ORCID,Calsavara Vinicius Fernando4ORCID,Brito Angelo Borsarelli Carvalho5,Silva Virgílio Sousa e5,Novello Roberto Gabriel Santiago5,Fernandes Thaissa Carvalho5,Decina Alessandra6,Dachez Roger7,Paterlini-Brechot Patrizia6ORCID

Affiliation:

1. Hcor Research Institute, São Paulo 04004-030, Brazil

2. Hospital Amaral Carvalho, Jaú, São Paulo 17210-080, Brazil

3. Department of Farmacology, Federal University of São Paulo (UNIFESP), São Paulo 04044-020, Brazil

4. Department of Computational Biomedicine, Biostatistics Shared Resource, Cedars-Sinai Cancer Center, Los Angeles, CA 90069, USA

5. Department of Clinical Oncology, A.C. Camargo Cancer Center, São Paulo 01509-900, Brazil

6. Rarecells Faculté de Médecine Necker, 160 rue de Vaugirard, 75015 Paris, France

7. Cytopathology Laboratory Innodiag, F-92100 Boulogne-Billancourt, France

Abstract

Polyploid Giant Cancer Cells (PGCCs) have been recognized as tumor cells that are resistant to anticancer therapies. However, it remains unclear whether their presence in the bloodstream can be consistently detected and utilized as a clinical marker to guide therapeutic anticancer regimens. To address these questions, we conducted a retrospective study involving 228 patients diagnosed with six different types of carcinomas (colon, gastric, NSCLC, breast, anal canal, kidney), with the majority of them (70%) being non-metastatic. Employing a highly sensitive liquid biopsy approach, ISET®, and cytopathological readout, we isolated and detected circulating PGCCs in the patients’ blood samples. PGCCs were identified in 46 (20.18%) out of 228 patients, including in 14.47% of 152 non-metastatic and 29.85% of 67 metastatic cases. Patients were subsequently monitored for a mean follow up period of 44.74 months (95%CI: 33.39–55.79 months). Remarkably, the presence of circulating PGCCs emerged as a statistically significant indicator of poor overall survival. Our findings suggest that circulating PGCCs hold promise as a reliable prognostic indicator. They underscore the importance of further extensive investigations into the role of circulating PGCCs as a prognostic marker and the development of anti-PGCC therapeutic strategies to improve cancer management and patient survival.

Funder

FAPESP

Publisher

MDPI AG

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