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Detection of Circulating Tumor Cells in Cerebrospinal Fluid of Patients with Suspected Breast Cancer Leptomeningeal Metastases: A Prospective Study.
Darlix, Amélie; Cayrefourcq, Laure; Pouderoux, Stéphane; Menjot de Champfleur, Nicolas; Bievelez, Alexis; Jacot, William; Leaha, Cristina; Thezenas, Simon; Alix-Panabières, Catherine.
Affiliation
  • Darlix A; Department of Medical Oncology, Institut Régional du Cancer de Montpellier, University of Montpellier, Montpellier, France.
  • Cayrefourcq L; Institut de Génomique Fonctionnelle, INSERM, CNRS, University of Montpellier, Montpellier, France.
  • Pouderoux S; Laboratory of Rare Human Circulating Cells, University Medical Center of Montpellier, University of Montpellier, Montpellier, France.
  • Menjot de Champfleur N; CREEC, MIVEGEC, University of Montpellier, CNRS, IRD, Montpellier, France.
  • Bievelez A; Department of Medical Oncology, Institut Régional du Cancer de Montpellier, University of Montpellier, Montpellier, France.
  • Jacot W; Department of Neuroradiology, University of Montpellier, CHU Montpellier, Montpellier, France.
  • Leaha C; Biometrics Unit, Institut Régional du Cancer de Montpellier, University of Montpellier, Montpellier, France.
  • Thezenas S; Department of Medical Oncology, Institut Régional du Cancer de Montpellier, University of Montpellier, Montpellier, France.
  • Alix-Panabières C; Institut de Recherche en Cancérologie de Montpellier IRCM, INSERM U1194, University of Montpellier ; Montpellier, France.
Clin Chem ; 68(10): 1311-1322, 2022 10 06.
Article in En | MEDLINE | ID: mdl-35953885
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.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Breast Neoplasms / Neoplastic Cells, Circulating Type of study: Diagnostic_studies / Observational_studies / Risk_factors_studies Limits: Adult / Female / Humans Language: En Year: 2022 Type: Article

Full text: 1 Database: MEDLINE Main subject: Breast Neoplasms / Neoplastic Cells, Circulating Type of study: Diagnostic_studies / Observational_studies / Risk_factors_studies Limits: Adult / Female / Humans Language: En Year: 2022 Type: Article