Dominant chromosomal abnormalities in breast cancer metastasis to CNS as compared with systemic metastasis demonstrated by liquid biopsy.

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Authors: Maher Albitar, Wojciech Swat, Ahmad Charifa, Sally Agersborg, Adam Albitar, Omar H. Butt, Andrew L. Pecora, Andre Henri Goy, Stanley E. Waintraub
Cited by: 1

Abstract

1035 Background: Breast cancer (BrC) central nervous system (CNS) metastases are believed to be biologically and therapeutically distinct from systemic metastases. Detecting BrC metastasis to CNS using liquid biopsy (LBx) of the CSF is emerging as a reliable approach not only for confirming metastasis, but also for defining the molecular and biological characteristics of this metastasis. We compared the findings of LBx performed on CSF with those obtained by peripheral blood (PB) LBx. Methods: LBx was performed by next generation sequencing (NGS) of cell-free DNA and RNA (cfDNA/cfRNA) in PB plasma or CSF as well as RNA sequencing of CSF cell pellet. RNA sequencing was performed using a panel of almost 1600 genes and DNA sequencing using 302 genes. Results: Of the 339 tested CSF samples, 29 (8.5%) were negative for any mutation and 57 (16.8%) showed low level mutations characteristic of CHIP (clonal hematopoiesis of indeterminate potential). However, two samples showed only chromosomal gain or loss without mutations and 2 showed chromosomal abnormalities with CHIP but no cancer-related mutations. In contrast, 19 of 279 PB samples (6.8%) were negative for any abnormality and 33 (11.8%) had CHIP. One sample of the PB cases showed chromosomal abnormalities without cancer-related somatic mutations. Of the 253 positive CSF samples 207 (82.1%) showed chromosomal structural abnormalities while only 71 of the 227 positive PB samples (31.2%) showed chromosomal structural gain or loss (P

Fields of Study & Subjects

Brain Metastases and Treatment Cancer Genomics and Diagnostics CNS Lymphoma Diagnosis and Treatment

Publication details

Journal / source
Journal of Clinical Oncology
Publisher
American Society of Clinical Oncology (ASCO)
Volume
44
Issue
16_suppl
Pages
1035–1035
Publication date
27 May 2026
Language
EN