Prognostic Role of Circulating Tumor Cell Trajectories in Metastatic Colorectal Cancer.

CellSearch® circulating tumor cell trajectories circulating tumor cells liquid biopsy metastatic colorectal cancer precision medicine prognostic and predictive biomarkers

Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
16 04 2023
Historique:
received: 02 03 2023
revised: 13 04 2023
accepted: 14 04 2023
medline: 17 5 2023
pubmed: 16 5 2023
entrez: 16 5 2023
Statut: epublish

Résumé

A large amount of evidence from clinical studies has demonstrated that circulating tumor cells are strong predictors of outcomes in many cancers. However, the clinical significance of CTC enumeration in metastatic colorectal cancer is still questioned. The aim of this study was to evaluate the clinical value of CTC dynamics in mCRC patients receiving first-line treatments. Serial CTC data from 218 patients were used to identify CTC trajectory patterns during the course of treatment. CTCs were evaluated at baseline, at a first-time point check and at the radiological progression of the disease. CTC dynamics were correlated with clinical endpoints. Using a cut-off of ≥1 CTC/7.5 mL, four prognostic trajectories were outlined. The best prognosis was obtained for patients with no evidence of CTCs at any timepoints, with a significant difference compared to all other groups. Lower PFS and OS were recognized in group 4 (CTCs always positive) at 7 and 16 months, respectively. We confirmed the clinical value of CTC positivity, even with only one cell detected. CTC trajectories are better prognostic indicators than CTC enumeration at baseline. The reported prognostic groups might help to improve risk stratification, providing potential biomarkers to monitor first-line treatments.

Sections du résumé

BACKGROUND
A large amount of evidence from clinical studies has demonstrated that circulating tumor cells are strong predictors of outcomes in many cancers. However, the clinical significance of CTC enumeration in metastatic colorectal cancer is still questioned. The aim of this study was to evaluate the clinical value of CTC dynamics in mCRC patients receiving first-line treatments.
MATERIALS AND METHODS
Serial CTC data from 218 patients were used to identify CTC trajectory patterns during the course of treatment. CTCs were evaluated at baseline, at a first-time point check and at the radiological progression of the disease. CTC dynamics were correlated with clinical endpoints.
RESULTS
Using a cut-off of ≥1 CTC/7.5 mL, four prognostic trajectories were outlined. The best prognosis was obtained for patients with no evidence of CTCs at any timepoints, with a significant difference compared to all other groups. Lower PFS and OS were recognized in group 4 (CTCs always positive) at 7 and 16 months, respectively.
CONCLUSIONS
We confirmed the clinical value of CTC positivity, even with only one cell detected. CTC trajectories are better prognostic indicators than CTC enumeration at baseline. The reported prognostic groups might help to improve risk stratification, providing potential biomarkers to monitor first-line treatments.

Identifiants

pubmed: 37190081
pii: cells12081172
doi: 10.3390/cells12081172
pmc: PMC10136568
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Valentina Magri (V)

Department of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy.

Luca Marino (L)

Department of Mechanical and Aerospace Engineering, Sapienza University of Rome, 00184 Rome, Italy.

Chiara Nicolazzo (C)

Department of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.

Angela Gradilone (A)

Department of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.

Gianluigi De Renzi (G)

Department of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.

Michela De Meo (M)

Department of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.

Orietta Gandini (O)

Department of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.

Arianna Sabatini (A)

Department of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy.

Daniele Santini (D)

Department of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy.

Enrico Cortesi (E)

Department of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy.

Paola Gazzaniga (P)

Department of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.

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