High Cell-Free DNA Levels in Cerebrospinal Fluid Predict Leptomeningeal Seeding of Hematologic Malignancy

The main difficulty when diagnosing leptomeningeal metastases (LMSs) is the low sensitivity of cytology. Cancer cells release cell-free DNA (cfDNA) during proliferation and apoptosis, and so we analyzed the cfDNA level as a biomarker for LMSs in hematologic malignancy.BACKGROUND AND PURPOSEThe main...

Full description

Saved in:
Bibliographic Details
Published inJournal of clinical neurology (Seoul, Korea) Vol. 16; no. 4; pp. 581 - 585
Main Authors Kim, Eun Young, Lee, Soon-Tae, Kim, Young-Sook, Byun, Ja Min, Hong, Junshik, Shin, Dong-Yeop, Koh, Youngil, Kim, Inho
Format Journal Article
LanguageEnglish
Published Korean Neurological Association 01.10.2020
대한신경과학회
Subjects
Online AccessGet full text
ISSN1738-6586
2005-5013
DOI10.3988/jcn.2020.16.4.581

Cover

More Information
Summary:The main difficulty when diagnosing leptomeningeal metastases (LMSs) is the low sensitivity of cytology. Cancer cells release cell-free DNA (cfDNA) during proliferation and apoptosis, and so we analyzed the cfDNA level as a biomarker for LMSs in hematologic malignancy.BACKGROUND AND PURPOSEThe main difficulty when diagnosing leptomeningeal metastases (LMSs) is the low sensitivity of cytology. Cancer cells release cell-free DNA (cfDNA) during proliferation and apoptosis, and so we analyzed the cfDNA level as a biomarker for LMSs in hematologic malignancy.This study prospectively enrolled 20 patients with hematologic malignancy who underwent cerebrospinal fluid (CSF) analysis. LMS was diagnosed based on both CSF cytology and clinical findings.METHODSThis study prospectively enrolled 20 patients with hematologic malignancy who underwent cerebrospinal fluid (CSF) analysis. LMS was diagnosed based on both CSF cytology and clinical findings.The CSF level of cfDNA was higher in patients with LMSs (108.17±84.84 ng/mL, mean±standard deviation) than in non-LMS patients (14.23±2.78 ng/mL). The sensitivity of cfDNA was higher than that of cytology (100% vs. 87%).RESULTSThe CSF level of cfDNA was higher in patients with LMSs (108.17±84.84 ng/mL, mean±standard deviation) than in non-LMS patients (14.23±2.78 ng/mL). The sensitivity of cfDNA was higher than that of cytology (100% vs. 87%).The cfDNA level in the CSF can be used as a supplemental marker for diagnosing LMS in hematologic malignancy patients.CONCLUSIONSThe cfDNA level in the CSF can be used as a supplemental marker for diagnosing LMS in hematologic malignancy patients.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Current address: Department of Neurology, Chungnam National University Sejong Hospital, Sejong, Korea.
These authors are co-first authors.
https://doi.org/10.3988/jcn.2020.16.4.581
ISSN:1738-6586
2005-5013
DOI:10.3988/jcn.2020.16.4.581