
Dr. Yuan discusses the ASCENT-03 trial's efficacy, crossover implications, and safety data for sacituzumab govitecan in cancer treatment.

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Jason Mouabbi, MD, is an assistant professor in the Department of Breast Medical Oncology in the Division of Cancer Medicine at The University of Texas MD Anderson Cancer Center in Houston.

Dr. Yuan discusses the ASCENT-03 trial's efficacy, crossover implications, and safety data for sacituzumab govitecan in cancer treatment.

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Jason Aboudi Mouabbi, MD, discussed the importance of using ctDNA testing to inform treatment decision-making across breast cancer populations.

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Panelists note that detecting low-level circulating tumor DNA (ctDNA) despite normal imaging presents a clinical challenge, requiring personalized management that balances early intervention with patient-centered communication, as this molecular signal offers a valuable window to detect and treat microscopic disease before overt recurrence.

Panelists highlight that advances in circulating tumor DNA (ctDNA) testing now enable detection of cancer at ultralow levels far earlier than traditional methods, offering new opportunities for timely intervention while emphasizing that negative results, though increasingly reliable, still require cautious interpretation to guide personalized treatment decisions.

Panelists emphasize that as circulating tumor DNA (ctDNA) testing becomes more integrated into clinical practice, careful interpretation, tailored testing schedules, and ongoing provider education are key to its effective use in personalized breast cancer care.

Panelists discuss the real-world challenges of managing patients with positive circulating tumor DNA (ctDNA) but no radiographic evidence of disease, emphasizing treatment intensification, genomic profiling for resistance mutations, dynamic monitoring, and the integration of ctDNA with imaging and biopsy to guide personalized breast cancer care.

Panelists discuss ongoing studies exploring circulating tumor DNA (ctDNA) use in the adjuvant breast cancer setting to detect recurrence earlier and guide therapy, highlighting advances in assay sensitivity, the choice between tumor-informed and tumor-agnostic tests, and the challenge of turning ctDNA’s strong prognostic value into actionable, outcome-improving interventions.

Panelists discuss how circulating tumor DNA (ctDNA) serves as a highly predictive prognostic biomarker in breast cancer, guiding personalized treatment intensification and informing important patient decisions while enhancing risk stratification and motivating proactive care despite ongoing research into its impact on long-term outcomes.

Panelists discuss how circulating tumor DNA (ctDNA) is becoming a vital biomarker in breast cancer, with its dynamic changes guiding personalized treatment decisions, serving as a surrogate end point in trials, enabling earlier detection of progression, and offering a less-invasive monitoring tool that complements imaging—especially benefiting patients with hard-to-monitor disease or those who are frail.

A panelist discusses how clinicians should exhaust all endocrine therapies plus targeted therapies before moving to chemotherapy or antibody-drug conjugates, while noting that different oral SERDs have varying adverse effect profiles that patients should be counseled about.

A panelist discusses how the EMBER-3 study results cannot be directly compared to those from EMERALD because of different patient populations, with EMBER-3 having fewer heavily pretreated patients and different baseline characteristics.

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