4.6 Article

Cerebrospinal fluid methylome-based liquid biopsies for accurate malignant brain neoplasm classification

Journal

NEURO-ONCOLOGY
Volume 25, Issue 8, Pages 1452-1460

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/neuonc/noac264

Keywords

brain cancer; cerebrospinal fluid; diagnostic biomarkers; DNA methylation; liquid biopsy

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By using methylomes obtained from cerebrospinal fluid, it is possible to accurately classify brain metastases, glioblastomas, and central nervous system lymphomas, which eliminates the risks associated with invasive diagnostic surgical biopsies and provides a classification basis for non-biopsiable tumors. This has significant implications for guiding surgical planning and avoiding surgical risks.
Background Resolving the differential diagnosis between brain metastases (BM), glioblastomas (GBM), and central nervous system lymphomas (CNSL) is an important dilemma for the clinical management of the main three intra-axial brain tumor types. Currently, treatment decisions require invasive diagnostic surgical biopsies that carry risks and morbidity. This study aimed to utilize methylomes from cerebrospinal fluid (CSF), a biofluid proximal to brain tumors, for reliable non-invasive classification that addresses limitations associated with low target abundance in existing approaches. Methods Binomial GLMnet classifiers of tumor type were built, in fifty iterations of 80% discovery sets, using CSF methylomes obtained from 57 BM, GBM, CNSL, and non-neoplastic control patients. Publicly-available tissue methylation profiles (N = 197) on these entities and normal brain parenchyma were used for validation and model optimization. Results Models reliably distinguished between BM (area under receiver operating characteristic curve [AUROC] = 0.93, 95% confidence interval [CI]: 0.71-1.0), GBM (AUROC = 0.83, 95% CI: 0.63-1.0), and CNSL (AUROC = 0.91, 95% CI: 0.66-1.0) in independent 20% validation sets. For validation, CSF-based methylome signatures reliably distinguished between tumor types within external tissue samples and tumors from non-neoplastic controls in CSF and tissue. CSF methylome signals were observed to align closely with tissue signatures for each entity. An additional set of optimized CSF-based models, built using tumor-specific features present in tissue data, showed enhanced classification accuracy. Conclusions CSF methylomes are reliable for liquid biopsy-based classification of the major three malignant brain tumor types. We discuss how liquid biopsies may impact brain cancer management in the future by avoiding surgical risks, classifying unbiopsiable tumors, and guiding surgical planning when resection is indicated.

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