Explore the Agenda
7:30 am Morning Check-In & Coffee
8:15 am Chair’s Opening Remarks
Transforming a Decade of Liquid Biopsy Progress into Routine Clinical Impact for Every Patient
8:20 am The Real-World Impact of Liquid Biopsy: The Patient Voice
As we open the 10th Liquid Biopsy for Precision Oncology Summit, we set aside the innovation & technology to begin with the perspective that matters most: the patient voice.
8:30 am 10 Years of Liquid Biopsy: Igniting a New Era in Precision Oncology
- Highlighting key scientific, technological, and regulatory milestones that have shaped the past decade of liquid biopsy innovation
- Identifying the most pressing challenges that still hinder broader adoption across trial phases, tumor types, and clinical settings
- Outlining the next strategic priorities needed to ensure liquid biopsies become a standard, validated tool for patient selection, monitoring, and treatment optimization in every clinical trial
9:00 am Supercharging Clinical Trials: Biomarkers for Smarter Enrollment & Monitoring
- Unlocking new patient populations with copy number loss detection
- Transforming drug development with machine learning-powered biomarkers
- Achieving highly sensitive MRD detection with a tissue-informed approach
9:30 am Confronting Complexity: Defining the Next Decade of Liquid Biopsy in Precision Oncology
- Confronting the translational hurdles that limit liquid biopsy adoption in drug development, from tumor heterogeneity and assay sensitivity to cost and trial feasibility
- Integrating emerging technologies such as methylation profiling and AI with the rigor required for clinical validation in oncology trials
- Defining how pharma decision-making will shape the path from exploratory assays to scalable, routine tools that deliver real patient impact
10:00 am Revolutionizing Precision Oncology Through Cutting-Edge Epigenomic Biomarkers & AI-Enabled Data Solutions
- Integrate genomic and epigenomic insights to enhance understanding of tumor behavior
- Leverage ctDNA and epigenomic biomarkers for response prediction, cancer subtyping, and detection of treatment-emergent resistance
- Explore how Guardant Infinity and InfinityAI unite innovative testing with multimodal data solutions to deliver novel epigenomics biomarkers from research to clinic
10:30 am Morning Break & Speed Networking
As the liquid biopsy community comes together for the 10th anniversary meeting, this dedicated session is designed to help you build meaningful new connections. All attendees will have the chance to meet peers across pharma, biotech, diagnostics and academia, ensuring valuable relationships that extend beyond the summit.
Standardizing Liquid Biopsies to Drive Reliable, Scalable Adoption Across Trials & Clinical Practice
11:30 am Interactive Session: Breaking Down Standardization Barriers Through Consistent Terminology & Metrics to Boost Liquid Biopsy Adoption
- What are the key roadblocks that continue to hinder standardization across liquid biopsy platforms, assays, and reporting?
- Establishing shared definitions, thresholds, and response criteria to align a fragmented field
- Building a practical roadmap for standardization, including actionable milestones and measurable impact to track progress and build confidence
12:00 pm Building the Ecosystem to Change Care: From Ultrasensitive MRD to Clinical Impact
- Earlier Intervention in High Risk Populations: With >250,000 patients tested in 2025, Natera has established access to a previously under-characterized but clinically meaningful population—enabling development in earlier disease settings where relapse risk is high and therapeutic impact may be greatest
- The Integration of Sensitivity and Scale: With the integration of Foresight’s phased-variant technology into the Signatera™ platform, Natera combines ultrasensitive detection capabilities below 0.1ppm with an expansive commercial and operational infrastructure to support MRD-guided studies at scale
- De-risking MRD-guided Development: Natera’s ecosystem of trial-enablement tools, including site selection support, real-world insights, and commercial-to-trial enrollment pathways, enables more efficient, lower-risk development
12:30 pm Enhancing Liquid Biopsy Toolkit with Epigenomics: From Cancer Detection to Treatment Response
- Non-invasive profiling of gene activity with epigenomics
- Holistic tumor-naïve biological insights
- Dynamic monitoring of therapy response and resistance
1:00 pm Panel Discussion: Bridging the Gap from Innovation to Access by Aligning Standardization, Policy & Reimbursement for Liquid Biopsy
- Uncovering how inconsistent definitions, metrics, and data standards are hindering payer confidence and policy support for liquid biopsy
- Exploring the role of pre-competitive collaboration in driving standardization to unlock broader reimbursement and clinical adoption
- Identifying immediate policy actions and evidence needs to align stakeholders and accelerate access to serial testing and early detection
1:30 pm Lunch Break & Networking
Track A: Preclinical Development & Early Translational
Embedding Robust Analytical Validation into Translational Studies to Drive Clinical Success – Chaired by
2:20 pm Underpinning the Value of Urine for Predictive & Monitoring Biomarkers in Bladder Cancer
- Urine-based LBx for patient selection in bladder cancer
- Implementation of urine-based LBx in clinical practice as a non-invasive testing option
- Future applications of urine-based LBx, including MRD and patient monitoring
2:45 pm Optimizing Pre-Analytical Variables for ctDNA, cfRNA/miRNA, EVs & Proteins: Practical Guidance for Trial-Ready Liquid Biopsy
- Key pre-analytical factors that influence sensitivity and reliability across ctDNA, cfRNA/miRNA, EVs, and protein biomarkers
- Practical guidance on tube selection, centrifugation workflows, and processing timelines
- How to navigate tradeoffs when designing multi-analyte liquid biopsy protocols
- Essential QC considerations to ensure trial-ready, reproducible liquid biopsy samples
3:15 pm Panel Discussion: Overcoming Sensitivity & Specificity Challenges to Deliver Reliable Liquid Biopsy Results at Scale
- Defining and achieving the optimal analytical thresholds for sensitivity and specificity in line with intended clinical use – how sensitive is too sensitive?
- Discussing strategies to minimize CHIP related false positives and false negatives without compromising turnaround time or trial feasibility
- Refining analytical validation data strategies to support regulatory submissions, companion diagnostic partnerships, and confident clinical decision-making
3:45 pm A Multicenter European Laboratory Evaluation of a Rapid End-to-End Liquid Biopsy NGS Solution for Genomic Testing in Advanced NSCLC
- Timely and comprehensive molecular profiling is essential for guiding treatment decisions in advanced non–small cell lung cancer (NSCLC). Liquid biopsy–based NGS approaches offer a minimally invasive means to support biomarker testing, particularly where tissue is limited or unavailable
- End-to-end liquid biopsy NGS solutions designed for decentralized implementation may help expand access to molecular testing by enabling use in smaller laboratories equipped with low- to medium-throughput sequencing platforms, while supporting clinically relevant turnaround times
- Current kitted liquid biopsy assays generally fall into amplicon-based targeted panels or hybrid capture–based comprehensive genomic profiling approaches, each associated with distinct workflow requirements, sequencing demands, and genomic coverage
- In this multicenter European evaluation, we present a rapid, targeted liquid biopsy NGS solution for advanced NSCLC. We assess workflow feasibility, sequencing requirements, and turnaround time, and discuss the potential role of such approaches in supporting decentralized molecular testing for lung cancer patients
Track B: Clinical Development & Commercialization
Driving Clinical Validation to Enhance Decision-Making & Accelerate Diagnostic Approval – Chaired by
2:20 pm Utility of ctDNA for Response Assessment of Solid Tumors Treated with Personalized Cancer Immunotherapy
- Demonstrating how ctDNA identifies molecular response and tracks response duration where MRI-based RECIST lacks clarity
- Leveraging ctDNA alongside imaging to enable earlier and more accurate detection of therapeutic benefit in second-line advanced HCC
- Using ctDNA-guided monitoring as an exploratory endpoint to inform trial design, optimize treatment strategies, and lay the groundwork for broader regulatory acceptance
2:45 pm Redefining the Limits: How Tumor-Informed Ultrasensitivity is Transforming the Landscape of Liquid Biopsy & Cancer Monitoring
- Detection at 1-3 PPM: Leveraging tumor-informed ultrasensitivity to detect trace molecular signals previously beyond the reach of standard liquid biopsy
- Enhanced Clinical Endpoints: Identifying therapy responders faster than traditional imaging through validated MRD monitoring across multiple cancer indications
- Accelerated Drug Development: Streamlining trial enrichment to facilitate the use of MRD as a surrogate endpoint
3:15 pm Panel Discussion: Clinically Validating Liquid Biopsies for Early Clinical Endpoints in Solid Tumor to Enhance Patient Selection & Monitoring
- What evidence and study designs are most critical to clinically validate liquid biopsies as early endpoints in trials, and how do these differ across indications?
- How can validated liquid biopsy endpoints improve patient selection and ongoing monitoring to accelerate therapeutic development and decision-making?
- Considerations into choosing the right test for the right applications.
3:45 pm Leveraging Ultrasensitive Liquid Biopsy Solutions for Longitudinal Monitoring & Treatment Response in Global Testing
- Learn about clinically validated liquid biopsy CGP and MRD solutions developed to support global patient management clinical trials
- Explore the latest data demonstrating how parallel sequencing of plasma and buffy coat can filter CH variants for more accurate variant detection to enable monitoring and treatment response
- Review early updates on improved sensitivity of MRD applications for earlier detection of relapse, novel endpoints and precise treatment decision
4:15 pm Afternoon Poster Session
Join the liquid biopsy community for an interactive poster session showcasing pioneering ctDNA research, breakthrough LBx technologies & assays, and real world solutions to accelerate clinical adoption. The session is open for all registered stakeholders to attend, learn, ask questions & build new connections. See full T&Cs online for eligibility.
Harnessing Novel AI, Methylation & Cutting-Edge Technology to Unlock Unprecedented Liquid Biopsy Insights
4:45 pm Leveraging Mutation & Methylation-Based ctDNA Profiling to Capture Tumor Heterogeneity & Enhance Clinical Readouts
- Demonstrating how broader ctDNA panels extend beyond single-gene tracking in advanced cancer, as a surrogate readout of clinical efficacy and to reveal tumor heterogeneity and evolving drivers of resistance
- Lessons from applying methylation-based sequencing approaches in oncology trials, including challenges in data interpretation and reporting
- Opportunities and limitations of integrating fragmentomics insights derived from methylation data to complement response monitoring in advanced disease
5:10 pm Liquid Biopsy Across the Drug Lifecycle: Discovery, Differentiation & Adoption
- Showing how Amgen leverages ctDNA and other modalities across discovery, clinical development, and commercialization to accelerate differentiation, regulatory approvals, and market adoption
- Highlighting case studies where ctDNA and liquid biopsy analyses informed dose selection, early efficacy readouts, and patient stratification, directly supporting faster decisionmaking and clinical success
- Discussing how Amgen generates the biomarker evidence base needed for regulators, payers, and clinicians to embrace liquid biopsy as a standard tool in advancing precision medicine
5:40 pm Advancing Precision Oncology through ctDNA Dynamics
- Exploring how ctDNA dynamics, including methylation patterns, can be leveraged to evaluate therapeutic response and inform treatment decisions
- Discussing the translational value of ctDNA analyses in uncovering mechanisms of resistance and guiding precisionoriented therapies
- Highlighting opportunities to integrate ctDNA into routine clinical workflows to better monitor tumor evolution and improve outcomes for patients with hard-to-treat cancer
6:05 pm Drinks Reception, Hosted by Foundation Medicine
7:05 pm Evening Engager, Hosted by Foundation Medicine
This session will bring together precision medicine experts to discuss how the latest generation of biomarkers are driving smarter trial enrollment and monitoring.
Enjoy dinner, networking, and a panel discussion on opportunities for emerging biomarkers to impact clinical trial design.