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Serial Postoperative Circulating Tumor DNA Assessment Has Strong Prognostic Value During Long-Term Follow-Up in Patients With Breast Cancer

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posted on 2025-12-01, 11:51 authored by Jacqueline ShawJacqueline Shaw, Karen PageKaren Page, Evie Wren, Elza C de Bruin, Ekaterina Kalashnikova, Robert Hastings, Rob McEwen, Eddie Zhang, Marc Wadsley, Emmanuel AcheampongEmmanuel Acheampong, Derek Renner, Kelly LT Gleason, Bana Ambasager, Daniel Stetson, Daniel Fernandez-Garcia, David GutteryDavid Guttery, Rebecca AllsoppRebecca Allsopp, Angel Rodriguez, Bernhard Zimmermann, Himanshu Sethi, Alexey Aleshin, Minetta C Liu, Cathy Richards, Justin Stebbing, Simak Ali, Farah Rehman, Susan Cleator, Laura Kenny, Samreen Ahmed, Anne C Armstrong, R Charles Coombes
PURPOSE Here, we report the sensitivity of a personalized, tumor-informed circulating tumor DNA (ctDNA) assay (Signatera) for detection of molecular relapse during long-term follow-up of patients with breast cancer. METHODS A total of 156 patients with primary breast cancer were monitored clinically for up to 12 years after surgery and adjuvant chemotherapy. Semiannual blood samples were prospectively collected, and analyzed retrospectively to detect residual disease by ultradeep sequencing using ctDNA assays, developed from primary tumor whole-exome sequencing data. RESULTS Personalized Signatera assays detected ctDNA ahead of clinical or radiologic relapse in 30 of the 34 patients who relapsed (patient-level sensitivity of 88.2%). Relapse was predicted with a lead interval of up to 38 months (median, 10.5 months; range, 0-38 months), and ctDNA positivity was associated with shorter relapse-free survival ( P < .0001) and overall survival ( P < .0001). All relapsing triple-negative patients (n = 7/23) had a ctDNA-positive test within a median of 8 months (range, 0-19 months), while the 16 nonrelapsed patients with triple-negative breast cancer remained ctDNA-negative during a median follow-up of 58 months (range, 8-99 months). The four patients who had negative tests before relapse all had hormone receptor–positive (HR+) disease and conversely, five of the 122 nonrelapsed patients (all HR+) had an occasional positive test. CONCLUSION Serial postoperative ctDNA assessment has strong prognostic value, provides a potential window for earlier therapeutic intervention, and may enable more effective monitoring than current clinical tests such as cancer antigen 15-3. Our study provides evidence that those with serially negative ctDNA tests have superior clinical outcomes, providing reassurance to patients with breast cancer. For select cases with HR+ disease, decisions about treatment management might require serial monitoring despite the ctDNA-positive result.<p></p>

Funding

Cancer Research UK Imperial Centre, the Leicester and Imperial Experimental Cancer Medicine Centers (ECMC) and NIHR BRCs

History

Author affiliation

University of Leicester Archive/Legacy Records College of Life Sciences Genetics, Genome Biology & Cancer Sciences Medical Sciences

Version

  • VoR (Version of Record)

Published in

JCO Precision Oncology

Volume

8

Issue

8

Pagination

e2300456

Publisher

American Society of Clinical Oncology (ASCO)

issn

2473-4284

eissn

2473-4284

Copyright date

2024

Available date

2025-12-01

Notes

Erratum https://ascopubs.org/doi/10.1200/PO.24.00310

Spatial coverage

United States

Language

en

Deposited by

Dr Karen Page

Deposit date

2025-11-21

Data Access Statement

Will individual participant data be available: yes. What participant data will be available: individual participant data that underlie the results reported in this article after deidentification (text, table figures, and supplemental data files). What other documents will be available: study protocol. When will data be available: immediately after publication. With whom: researchers providing a methodologically sound proposal. For what type of analyses: to achieve the aims of the proposal. By what mechanism will data be made available: to gain access data requestors will need to sign a data access agreement.

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