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Prognostic value of cerebrospinal fluid tumor cell count in leptomeningeal disease from solid tumors.
Barbour, Andrew B; Blouw, Barbara; Taylor, Lynne P; Graber, Jerome J; McGranahan, Tresa; Blau, Molly; Halasz, Lia M; Lo, Simon S; Tseng, Yolanda D; Venur, Vyshak; Yang, Jonathan T.
Afiliação
  • Barbour AB; Department of Radiation Oncology, University of Washington- Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Blouw B; Formerly Employed at Biocept, San Diego, CA, USA.
  • Taylor LP; Department of Neurology, University of Washington- Alvord Brain Tumor Center, Seattle, WA, USA.
  • Graber JJ; Department of Neurology, University of Washington- Alvord Brain Tumor Center, Seattle, WA, USA.
  • McGranahan T; Division of Hematology-Oncology, Scripps Cancer Center, La Jolla, CA, USA.
  • Blau M; Department of Radiation Oncology, University of Washington- Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Halasz LM; Department of Radiation Oncology, University of Washington- Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Lo SS; Department of Radiation Oncology, University of Washington- Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Tseng YD; Department of Radiation Oncology, University of Washington- Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Venur V; Department of Neurology, University of Washington- Alvord Brain Tumor Center, Seattle, WA, USA.
  • Yang JT; Division of Medical Oncology, University of Washington- Fred Hutchinson Cancer Center, Seattle, WA, USA.
J Neurooncol ; 167(3): 509-514, 2024 May.
Article em En | MEDLINE | ID: mdl-38441840
ABSTRACT

PURPOSE:

Treatment decisions for leptomeningeal disease (LMD) rely on patient risk stratification, since clinicians lack objective prognostic tools. The introduction of rare cell capture technology for identification of cerebrospinal fluid tumor cells (CSF-TCs), such as CNSide assay, improved the sensitivity of LMD diagnosis, but prognostic value is unknown. This study assesses the prognostic value of CSF-TC density in patients with LMD from solid tumors.

METHODS:

We conducted a retrospective cohort study of patients with newly diagnosed or previously treated LMD from a single institution who had CNSide assay testing for CSF-TCs from 2020 to 2023. Univariable and multivariable survival analyses were conducted with Cox proportional-hazards modeling. Maximally-selected rank statistics were used to determine an optimal cutpoint for CSF-TC density and survival.

RESULTS:

Of 31 patients, 29 had CSF-TCs detected on CNSide. Median (interquartile range [IQR]) CSF-TC density was 67.8 (4.7-639) TCs/mL. CSF cytology was positive in 16 of 29 patients with positive CNSide (CNSide diagnostic sensitivity = 93.5%, negative predictive value = 85.7%). Median (IQR) survival from time of CSF-TC detection was 176 (89-481) days. On univariable and multivariable analysis, CSF-TC density was significantly associated with survival. An optimal cutpoint for dichotomizing survival by CSF-TC density was 19.34 TCs/mL. The time-dependent sensitivity and specificity for survival using this stratification were 76% and 67% at 6 months and 65% and 67% at 1 year, respectively.

CONCLUSIONS:

CSF-TC density may carry prognostic value in patients with LMD from solid tumors. Integrating CSF-TC density into LMD patient risk-stratification may help guide treatment decisions.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Meníngeas Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurooncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Meníngeas Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurooncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos