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Evaluation of a Liquid Biopsy-Breast Cancer Methylation (LBx-BCM) Cartridge Assay for Predicting Early Disease Progression and Survival: TBCRC 005 Prospective Trial

Authors :
Kala Visvanathan
Leslie Cope
Mary Jo Fackler
Michael Considine
Lori Sokoll
Lisa A. Carey
Andres Forero-Torres
James N. Ingle
Nancy U. Lin
Rita Nanda
Anna Maria Storniolo
Suzana Tulac
Neesha Venkatesan
Natalie C. Wu
Sudhakar Marla
Scott Campbell
Michael Bates
Christopher B. Umbricht
Antonio C. Wolff
Saraswati Sukumar
Source :
Clinical Cancer Research. 29:784-790
Publication Year :
2022
Publisher :
American Association for Cancer Research (AACR), 2022.

Abstract

Purpose:We previously demonstrated that high levels of circulating methylated DNA are associated with subsequent disease progression in women with metastatic breast cancer (MBC). In this study, we evaluated the clinical utility of a novel liquid biopsy-breast cancer methylation (LBx-BCM) prototype assay using the GeneXpert cartridge system for early assessment of disease progression in MBC.Experimental Design:The 9-marker LBx-BCM prototype assay was evaluated in TBCRC 005, a prospective biomarker study, using plasma collected at baseline, week 4, and week 8 from 144 patients with MBC.Results:At week 4, patients with MBC with high cumulative methylation (CM) had a significantly shorter median PFS (2.88 months vs. 6.60 months, P = 0.001) and OS (14.52 months vs. 22.44 months, P = 0.005) compared with those with low CM. In a multivariable model, high versus low CM was also associated with shorter PFS (HR, 1.90; 95% CI, 1.20–3.01; P = 0.006). Change in CM from baseline to week 4 (OR, 4.60; 95% CI, 1.77–11.93; P = 0.002) and high levels of CM at week 4 (OR, 2.78; 95% CI, 1.29–5.99; P = 0.009) were associated with progressive disease at the time of first restaging. A robust risk model based on week 4 circulating CM levels was developed to predict disease progression as early as 3 months after initiating a new treatment.Conclusions:The automated LBx-BCM prototype assay is a promising clinical tool for detecting disease progression a month after initiating treatment in women with MBC undergoing routine care. The next step is to validate its clinical utility for specific treatments.

Subjects

Subjects :
Cancer Research
Oncology

Details

ISSN :
15573265 and 10780432
Volume :
29
Database :
OpenAIRE
Journal :
Clinical Cancer Research
Accession number :
edsair.doi.dedup.....4bb26af617fa696a01dd03477d46377a
Full Text :
https://doi.org/10.1158/1078-0432.ccr-22-2128