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The Pathologist / Issues / 2026 / October / The Fluid Future of Liquid Biopsy
Oncology Liquid biopsy Omics Precision medicine Technology and innovation Molecular Pathology

The Fluid Future of Liquid Biopsy

Clinical lab scientists will help expand ctDNA applications from what can be measured to what should be measured, and why

By Patrick Hurban 10/14/2026 Discussion 5 min read
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Clinical Scorecard: The Fluid Future of Liquid Biopsy

At a Glance

CategoryDetail
ConditionLiquid biopsy in precision oncology
Key MechanismsAnalysis of circulating tumor DNA (ctDNA), including tumor-specific mutations, cancer-associated methylation patterns, and DNA fragment characteristics, for molecular assessment and longitudinal monitoring.
Target PopulationPeople with cancer, including patients undergoing curative-intent treatment and those with metastatic disease; the article discusses studies across multiple cancer types.
Care SettingOncology care and clinical laboratory settings, where liquid biopsy is discussed as a complement to tissue testing for treatment assessment and disease monitoring.

Key Highlights

  • Liquid biopsy can provide molecular information without repeated tumor-tissue sampling and supports serial assessment during treatment.
  • Across studies presented at ASCO 2026, post-treatment ctDNA positivity was associated with worse disease-free survival or distant recurrence risk.
  • In early triple-negative breast cancer, a study reported that ctDNA surveillance detected MRD before clinical or radiographic evidence of relapse.
  • Researchers are evaluating mutation, methylation, and fragmentomic signals together to improve sensitivity and add biological context.
  • Results described for daraxonrasib in previously treated metastatic pancreatic cancer showed activity in KRAS-mutant and non-mutant populations.

Guideline-Based Recommendations

Diagnosis

  • The article describes liquid biopsy as complementary to tissue sampling and does not recommend replacing tissue testing.
  • The article describes MRD approaches that identify tumor-specific mutations and search for them in circulating free DNA.

Management

  • The article states that serial liquid-biopsy assessments may inform decisions about continuing or modifying treatment.
  • The article reports prognostic and surveillance findings but does not establish a treatment algorithm based on ctDNA results.

Monitoring & Follow-up

  • The article describes liquid biopsy as enabling longitudinal assessment of tumor evolution, treatment response, and recurrence risk.
  • In a Phase 2 study of early triple-negative breast cancer, ctDNA surveillance detected MRD before clinical or radiographic evidence of relapse.

Risks

  • The article identifies sensitivity in distinguishing rare tumor-derived DNA from normal circulating DNA as a challenge.
  • The article raises questions about the added predictive value, complexity, cost, and laboratory consistency of multimodal testing.

Patient & Prescribing Data

The article discusses patients with cancer across tumor types, including patients after curative-intent treatment, patients with early triple-negative breast cancer, and patients with previously treated metastatic pancreatic cancer.

The article describes ctDNA as a potential source of prognostic and monitoring information. It reports daraxonrasib activity across KRAS-mutant and non-mutant populations in the RASolute 302 Phase III study; it provides no prescribing instructions or dosing information.

Clinical Best Practices

  • The article frames liquid biopsy as complementary to tissue sampling, not as a universal replacement.
  • The article reports prognostic associations and early MRD detection but does not specify a treatment response to a positive ctDNA result.
  • The article describes mutation, methylation, and fragmentomic approaches as under evaluation and raises questions about predictive value, cost, and consistent laboratory implementation.

Related Resources & Content

This content is an AI-generated, fully rewritten summary based on a published scholarly article. It does not reproduce the original text and is not a substitute for the original publication. Readers are encouraged to consult the source for full context, data, and methodology.

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About the Author(s)

Patrick Hurban

Patrick Hurban, PhD, is a seasoned scientific leader at IQVIA Laboratories, currently serving as Chief Scientific Officer for Laboratories and Design and Delivery Innovation. In this role, he drives global scientific strategy and innovation across laboratory services supporting clinical development. Patrick previously led genomics and translational science operations worldwide and spent over a decade heading translational genomics. Over more than 25 years in molecular genetics and RandD, Patrick has built high-performing teams that advance precision medicine and clinical research.

More Articles by Patrick Hurban

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