Association of post-operative ctDNA detection with outcomes of patients with early breast cancers
- R Cutts 1, L Ulrich 2, M Beaney 1, M Robert 3, M Coakley 1, C Bunce 4, G W Crestani 1, S Hrebien 1, E Kalashnikova 5, H-T Wu 5, S Dashner 5, H Sethi 5, A Aleshin 5, M Liu 5, A Ring 2, A Okines 2, I E Smith 2, P Barry 2, N C Turner 6, I Garcia-Murillas 1
- 1The Breast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London.
- 2Breast Unit, Royal Marsden Hospital, London, UK.
- 3Department of Breast Medical Oncology and Neuro-Oncology, Early Therapeutic Unit, Institute of Oncology de l'Ouest, St Herblain, France.
- 4Clinical Trials Unit, Royal Marsden Hospital, London, UK.
- 5Natera, Inc., Austin, USA.
- 6The Breast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London; Breast Unit, Royal Marsden Hospital, London, UK; The Ralph Lauren Centre for Breast Cancer Research, Royal Marsden Hospital, London, UK.
- 0The Breast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London.
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View abstract on PubMed
Summary
This summary is machine-generated.Circulating tumor DNA (ctDNA) analysis in early breast cancer patients after surgery can detect residual disease. Absence of ctDNA post-surgery is linked to better distant recurrence-free survival, suggesting potential for treatment de-escalation.
Area Of Science
- Oncology
- Molecular Diagnostics
- Genomics
Background
- Early breast cancer (EBC) management requires accurate prognostication.
- Assessing molecular residual disease (MRD) post-surgery is crucial for treatment decisions.
- Circulating tumor DNA (ctDNA) is a promising biomarker for MRD detection.
Purpose Of The Study
- To evaluate ctDNA detection after primary surgery in EBC patients.
- To determine if post-surgical ctDNA identifies MRD and predicts relapse.
- To associate ctDNA status with relapse-free survival (RFS) and distant recurrence-free survival (DRFS).
Main Methods
- Retrospective analysis of plasma samples from 48 EBC patients.
- Samples collected pre-surgery, post-surgery, and pre-adjuvant therapy.
- Personalized, tumor-informed ctDNA analysis using next-generation sequencing (Signatera™).
Main Results
- ctDNA was detected in 64.5% of patients pre-surgery and 35.4% post-surgery.
- Post-surgical ctDNA detection was associated with worse DRFS (HR=5.5, P=0.04).
- ctDNA detection anticipated clinical relapse by a median of 16 months.
Conclusions
- ctDNA is detectable in treatment-naive EBC patients after surgery.
- Absence of post-surgical ctDNA correlates with improved DRFS.
- These findings support trials investigating de-escalation of systemic therapy based on ctDNA status.
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