Detection of Circulating Tumor Cells in Cerebrospinal Fluid of Patients with Suspected Breast Cancer Leptomeningeal Metastases: A Prospective Study

Author:

Darlix Amélie12,Cayrefourcq Laure34,Pouderoux Stéphane1,Menjot de Champfleur Nicolas5,Bievelez Alexis6,Jacot William17,Leaha Cristina8,Thezenas Simon6,Alix-Panabières Catherine34ORCID

Affiliation:

1. Department of Medical Oncology, Institut Régional du Cancer de Montpellier, University of Montpellier , Montpellier , France

2. Institut de Génomique Fonctionnelle, INSERM, CNRS, University of Montpellier , Montpellier , France

3. Laboratory of Rare Human Circulating Cells, University Medical Center of Montpellier, University of Montpellier , Montpellier , France

4. CREEC, MIVEGEC, University of Montpellier, CNRS, IRD , Montpellier , France

5. Department of Neuroradiology, University of Montpellier, CHU Montpellier , Montpellier , France

6. Biometrics Unit, Institut Régional du Cancer de Montpellier, University of Montpellier , Montpellier , France

7. Institut de Recherche en Cancérologie de Montpellier IRCM, INSERM U1194, University of Montpellier ; Montpellier , France

8. Department of Pathology, Institut Régional du Cancer de Montpellier, University of Montpellier , Montpellier , France

Abstract

Abstract Background The diagnosis of breast cancer (BC)-related leptomeningeal metastases (LM) relies on the detection of tumor cells in cerebrospinal fluid (CSF) using conventional cytology (gold standard). However, the sensitivity of this technique is low. Our goal was to evaluate whether circulating tumor cell (CTC) detection in CSF using the CellSearch® system could be used for LM diagnosis. Methods This prospective, monocentric study included adult patients with suspected BC-related LM. The clinical sensitivity and specificity of CTC detection in CSF for LM diagnosis were calculated relative to conventional CSF cytology. Results Forty-nine eligible patients were included and 40 were evaluable (CTC detection technical failure: n = 8, eligibility criteria failure: n = 1). Cytology was positive in 18/40 patients. CTCs were detected in these 18 patients (median: 5824 CTC, range: 93 to 45052) and in 5/22 patients with negative cytology (median: 2 CTC, range: 1 to 44). The detection of ≥1 CSF CTC was associated with a clinical sensitivity of 100% (95% CI, 82.4–100) and a specificity of 77.3% (95% CI, 64.3–90.3) for LM diagnosis. HER2+ CTCs were detected in the CSF of 40.6% of patients with HER2− BC (median: 500 CTC, range: 13 to 28 320). Conclusions The clinical sensitivity of CTC detection in CSF with the CellSearch® system for LM diagnosis is higher than that of CSF cytology. CTC detection in patients with negative cytology, however, must be further investigated. The finding of HER2+ CTCs in patients with HER2− BC suggests that the HER2 status of LM should be evaluated to increase the treatment opportunities for these patients.

Funder

National Institute of Cancer

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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