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Interview with Pioneer Honoree: Dennis J. Slamon, UCLA

Interview with Pioneer Honoree: Dennis J. Slamon, UCLA

Keynote in Track 3 Day 2: Molecular Diversity of Human Malignacies: Diagnostic and Therapeutic Implications

PMWC 2026 Pioneer Honoree Track 3 Day 2 Keynote

1

The Future of Therapeutic Target Discovery

Dr. Slamon’s work on HER2 was a groundbreaking translation of a molecular target into a life-saving therapy. The next stage of liquid biopsy (ctDNA, fragmentomics, etc.) allows us to monitor minimal residual disease (MRD) and treatment resistance in real-time.

Question "Looking ahead, how will the real-time, non-invasive molecular intelligence provided by next-generation liquid biopsies transform not just how we monitor patients, but fundamentally change the way we discover and validate the next generation of therapeutic targets, moving beyond simple gene mutations to complex signatures like fragmentomics or methylation?"
A: The future of this emerging technology is extremely promising for changing the way we not only diagnose new cases, but how we manage active treatment cases. The fact that we may now be able to determine disease response and/or recurrence earlier than currently possible with anatomic imaging technologies will significantly enhance the way we manage our patients. It will allow for earlier intervention with potentially more effective alternative therapies when we know a patient is not responding to what is being used.

2

Overcoming Therapy Resistance

Dr. Slamon's pioneering work in the HR+/HER2- space, notably with CDK4/6 inhibitors (like Kisqali), has significantly improved outcomes for the largest population of breast cancer patients. However, resistance remains the biggest hurdle in extending curative outcomes.

Question "Your work was foundational in identifying the HER2 subtype, and now you are a leader in optimizing therapy for the HR+/HER2- subtype, which is seeing remarkable success with CDK4/6 inhibitors. As we push to eliminate relapse in this population, what specific molecular pathways or emerging resistance mechanisms—perhaps detectable only by new multi-omic liquid biopsy methods—do you believe offer the most urgent and actionable new targets for combination strategies?"
A: We have utilized next generation genomic and proteomic sequencing technologies to identify those molecular alterations and/or pathways associated with resistance mechanisms to targeted therapies. As stated above, these type of data could lead to even earlier alternative interventions when our initial therapies have fail to achieve the desired clinical outcomes.

3

Global Implementation and Access

Breakthroughs like Herceptin and ctDNA-based tools have the greatest impact when they reach patients everywhere. This question related to the final panel of Day 2 addresses "From Validation to Payment: Coverage Pathways."

Question "Given the proven ability of tumor-informed ctDNA tests to detect cancer’s return months before scans and guide therapy, what is the single biggest policy or infrastructure hurdle we must overcome in the next five years to ensure these advanced, personalized medicine tools are accessible and affordable for patients globally—not just at elite cancer centers?"
A: The validation that these newer technologies can give accurate information much earlier than the older anatomic-based methods of evaluating disease status could bring significant improvements in how we manage cancer. It would be very useful, indeed critical, to know when cessation of an approved but possibly ineffective therapeutic approach for an individual patient is failing to achieve the desired clinical effect. The sooner we have these type of data, the better for our patients and our ability to optimally manage their disease. That alone could result in significant savings to a health system where cancer drug costs are so high. In addition, the cost of deploying ct-effective and accurate genomic tests for screening, diagnostic and response assessment activity should make such an approach even more cost-effective than our many of our current anatomic-based methods for these decisions.
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