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

Author:

Visvanathan Kala1ORCID,Cope Leslie2ORCID,Fackler Mary Jo2ORCID,Considine Michael2ORCID,Sokoll Lori2ORCID,Carey Lisa A.3ORCID,Forero-Torres Andres4ORCID,Ingle James N.5ORCID,Lin Nancy U.6ORCID,Nanda Rita7ORCID,Storniolo Anna Maria8ORCID,Tulac Suzana9ORCID,Venkatesan Neesha9ORCID,Wu Natalie C.9ORCID,Marla Sudhakar9ORCID,Campbell Scott9ORCID,Bates Michael9ORCID,Umbricht Christopher B.2ORCID,Wolff Antonio C.2ORCID,Sukumar Saraswati2ORCID

Affiliation:

1. 1Johns Hopkins University School of Medicine and Bloomberg School of Public Health, Baltimore, Maryland.

2. 2Johns Hopkins University School of Medicine, Baltimore, Maryland.

3. 3University of North Carolina, Chapel Hill, North Carolina.

4. 4Seagen Bothell, Washington.

5. 5Mayo Clinic, Rochester, Minnesota.

6. 6Dana-Farber Cancer Institute, Boston, Massachusetts.

7. 7University of Chicago, Chicago, Illinois.

8. 8Indiana University, Indianapolis, Indiana.

9. 9Cepheid, Sunnyvale, California.

Abstract

AbstractPurpose: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.

Funder

U.S. Department of Defense

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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