Cerebrospinal fluid circulating tumor cells as a quantifiable measurement of leptomeningeal metastases in patients with HER2 positive cancer

Rachna Malani, Martin Fleisher, Priya Kumthekar, Xuling Lin, Antonio Omuro, Morris D. Groves, Nancy U. Lin, Michelle Melisko, Andrew B. Lassman, Suriya Jeyapalan, Andrew Seidman, Anna Skakodub, Adrienne Boire, Lisa M. DeAngelis, Marc Rosenblum, Jeffrey Raizer, Elena Pentsova*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

57 Scopus citations

Abstract

Purpose: The CellSearch® system has been used to identify circulating tumor cells (CTCs) in cerebrospinal fluid (CSF) to diagnose leptomeningeal metastasis (LM) in patients with epithelial cancers. Using this system, we prospectively explored sequential CSF CTC enumeration in patients with LM from HER2+ cancers receiving intrathecal (IT) trastuzumab to capture dynamic changes in CSF CTC enumeration. Methods: CSF from patients enrolled in an IRB-approved phase I/II dose escalation trial of IT trastuzumab for LM in HER2+ cancer (NCT01325207) was obtained on day 1 of each cycle and was evaluated by the CellSearch® platform for CTC enumeration. The results were correlated with CSF cytology from the same sample, along with clinical and radiographic response. Results: Fifteen out of 34 patients with HER2+ LM were enrolled in CSF CTC analysis; 14 were women. Radiographic LM was documented in 14 (93%) patients; CSF cytology was positive in 6 (40%) and CSF CTCs were identified in 13 (87%). Median CSF CTC was 22 CTCs (range 0–200 +) per 3 ml. HER2/neu expression analysis of CTCs was performed in 8 patients; 75% had confirmed expression of HER2/neu positivity in CSF and HER2/neu expression was absent in 25%. Four of 10 patients received 7 or more cycles of IT trastuzumab; in 3 of these patients, increase in CSF CTCs enumeration from baseline was detected 2–3 months prior to changes seen on MRI, and while CSF cytology remained negative. Conclusion: Our study demonstrates that enumeration of CSF CTCs may provide dynamic, quantitative assessment of tumor burden in the central nervous system compartment during treatment for LM and prior to changes on MRI or CSF cytology. Trial Registration: Clinicaltrials.gov: NCT01325207; registered March 29th, 2011.

Original languageEnglish (US)
Pages (from-to)599-606
Number of pages8
JournalJournal of Neuro-Oncology
Volume148
Issue number3
DOIs
StatePublished - Jul 1 2020

Funding

This research was supported by grants from the Memorial Sloan Kettering Brain Tumor Center and the National Institutes of Health/National Cancer Institute (P30-CA008748). Janssen Diagnostics (Menarini Silicon Biosystems) provided reagents for the analysis, but no financial support. Acknowledgements We thank Moira McGrath for her editorial assistance. Part of this study was presented at the American Society of Clinical Oncology meeting in Chicago, 2017, and the European Association of Neuro-Oncology meeting in Stockholm, 2018. This research was supported by grants from the Memorial Sloan Kettering Brain Tumor Center and the National Institutes of Health/National Cancer Institute (P30-CA008748).

Keywords

  • Biomarker
  • Cerebrospinal fluid
  • Circulating tumor cells
  • Leptomeningeal metastases
  • Liquid biomarkers

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology
  • Oncology
  • Cancer Research

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