Personalized circulating tumor DNA analysis to detect residual disease after neoadjuvant therapy in breast cancer

Author:

McDonald Bradon R.1ORCID,Contente-Cuomo Tania1,Sammut Stephen-John2ORCID,Odenheimer-Bergman Ahuva1,Ernst Brenda3ORCID,Perdigones Nieves1ORCID,Chin Suet-Feung2ORCID,Farooq Maria1ORCID,Mejia Rosa4,Cronin Patricia A.3,Anderson Karen S.35,Kosiorek Heidi E.3,Northfelt Donald W.3,McCullough Ann E.3ORCID,Patel Bhavika K.3ORCID,Weitzel Jeffrey N.4ORCID,Slavin Thomas P.4,Caldas Carlos2ORCID,Pockaj Barbara A.3ORCID,Murtaza Muhammed13ORCID

Affiliation:

1. Center for Noninvasive Diagnostics, Translational Genomics Research Institute, Phoenix, AZ 85004, USA.

2. Department of Oncology and Cancer Research UK Cambridge Institute and Cancer Centre, Li Ka Shing Centre, University of Cambridge, Cambridge CB2 0RE, UK.

3. Mayo Clinic, Scottsdale, AZ 85259, USA.

4. City of Hope, Duarte, CA 91010, USA.

5. Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.

Abstract

A robust personalized ctDNA test, TARDIS, achieves high accuracy for residual disease after completion of neoadjuvant therapy.

Funder

National Institutes of Health

V Foundation for Cancer Research

Science Foundation Arizona

Ben and Catherine Ivy Foundation

Cancer Research UK

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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