AI Article Synopsis

  • This review focuses on the use of circulating tumor DNA (ctDNA) as a biomarker to select breast cancer patients for treatment, examining current evidence and active trials in both early and metastatic stages.* -
  • In metastatic breast cancer, ctDNA analysis can reveal specific genetic changes that allow for targeted therapies; approved tests already exist for mutations like PIK3CA and ESR1 which guide treatment decisions.* -
  • In the early stages, ctDNA may help detect relapses up to 10 months earlier than traditional imaging, potentially leading to better treatment planning, although further validation through trials is necessary.*

Article Abstract

Purpose Of Review: This review aims to explore the role of circulating tumor DNA (ctDNA) as a biomarker for patient selection in breast cancer. We describe the current evidence and the main ongoing trials both in the early and metastatic setting.

Recent Findings: In the metastatic setting, the analysis of ctDNA can identify specific genetic alterations amenable of molecularly targeted treatments. Several assays are now approved for the detection of genetic alterations in plasma cell-free DNA to guide treatment decision (e.g., PIK3CA mutations for PI3K inhibitors, and ESR1 mutations for the selective estrogen receptor degrader elacestrant). In the early setting, emerging evidence is demonstrating that ctDNA can identify a disease relapse with a lead-time of approximately 10 months before imaging. This could help select patients who may benefit from escalation treatment strategy, although this hypothesis needs to be first prospectively validated.

Summary: Liquid biopsy for ctDNA detection represents an exciting new field in rapid evolution. Several trials are ongoing to validate the clinical utility of ctDNA in daily practice in the early setting and to expand its current indications in the metastatic one.

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Source
http://dx.doi.org/10.1097/CCO.0000000000000964DOI Listing

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