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A pilot study on the use of cerebrospinal fluid cell-free DNA in intramedullary spinal ependymoma.
Connolly, Ian David; Li, Yingmei; Pan, Wenying; Johnson, Eli; You, Linya; Vogel, Hannes; Ratliff, John; Hayden Gephart, Melanie.
Afiliação
  • Connolly ID; Department of Neurosurgery, Stanford University School of Medicine, 300 Pasteur Drive MC 5327, Stanford, CA, 94305, USA.
  • Li Y; Department of Neurosurgery, Stanford University School of Medicine, 300 Pasteur Drive MC 5327, Stanford, CA, 94305, USA.
  • Pan W; Department of Bioengineering, James H. Clark Center, Stanford University, Stanford, CA, USA.
  • Johnson E; Department of Neurosurgery, Stanford University School of Medicine, 300 Pasteur Drive MC 5327, Stanford, CA, 94305, USA.
  • You L; Department of Neurosurgery, Stanford University School of Medicine, 300 Pasteur Drive MC 5327, Stanford, CA, 94305, USA.
  • Vogel H; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Ratliff J; Department of Neurosurgery, Stanford University School of Medicine, 300 Pasteur Drive MC 5327, Stanford, CA, 94305, USA.
  • Hayden Gephart M; Department of Neurosurgery, Stanford University School of Medicine, 300 Pasteur Drive MC 5327, Stanford, CA, 94305, USA. mghayden@stanford.edu.
J Neurooncol ; 135(1): 29-36, 2017 Oct.
Article em En | MEDLINE | ID: mdl-28900844
ABSTRACT
Cerebrospinal fluid (CSF) represents a promising source of cell-free DNA (cfDNA) for tumors of the central nervous system. A CSF-based liquid biopsy may obviate the need for riskier tissue biopsies and serve as a means for monitoring tumor recurrence or response to therapy. Spinal ependymomas most commonly occur in adults, and aggressive resection must be delicately balanced with the risk of injury to adjacent normal tissue. In patients with subtotal resection, recurrence commonly occurs. A CSF-based liquid biopsy matched to the patient's spinal ependymoma mutation profile has potential to be more sensitive then surveillance MRI, but the utility has not been well characterized for tumors of the spinal cord. In this study, we collected matched blood, tumor, and CSF samples from three adult patients with WHO grade II intramedullary spinal ependymoma. We performed whole exome sequencing on matched tumor and normal DNA to design Droplet Digital™ PCR (ddPCR) probes for tumor and wild-type mutations. We then interrogated CSF samples for tumor-derived cfDNA by performing ddPCR on extracted cfDNA. Tumor cfDNA was not reliably detected in the CSF of our cohort. Anatomic sequestration and low grade of intramedullary spinal cord tumors likely limits the role of CSF liquid biopsy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Medula Espinal / Ependimoma / Ácidos Nucleicos Livres Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Medula Espinal / Ependimoma / Ácidos Nucleicos Livres Idioma: En Ano de publicação: 2017 Tipo de documento: Article