Optimising tissue acquisition and the molecular testing pathway for patients with non-small cell lung cancer: A UK

Neal Navani1, Rachel Butler2, Salma Ibrahimo3

  • 1Lungs for Living Research Centre, UCL Respiratory, University College London, London, United Kingdom; University College London Hospitals NHS Foundation Trust, London, United Kingdom.

Insights

Optimizing molecular testing for non-small cell lung cancer (NSCLC) is crucial for targeted therapies. This study offers best practice recommendations to address challenges in tissue acquisition and genomic testing pathways in the UK.

Area of Science:

  • Oncology
  • Genomics
  • Diagnostic Pathology

Background:

  • Targeted therapies for non-small cell lung cancer (NSCLC) rely on identifying actionable variants.
  • Molecular testing is essential for personalized treatment, improved outcomes, and reduced toxicity in NSCLC patients.
  • Recent reforms in UK genomic testing aim to standardize provision but face challenges.

Purpose of the Study:

  • To summarize expert-opinion-based best practice recommendations for UK molecular testing in NSCLC.
  • To address challenges in tissue acquisition and genomic testing pathways.
  • To optimize the use of genomic information for personalized cancer care.

Main Methods:

  • Review of current UK molecular testing pathways for NSCLC.
  • Expert opinion synthesis on best practices for tissue acquisition and sample processing.
  • Identification of challenges including tissue quality, adequacy, turnaround times, and standardization.

Main Results:

  • Recommends least invasive biopsy techniques for optimal tissue yield and quality.
  • Suggests considering sedation for patient comfort and rapid on-site evaluation for adequate sampling.
  • Highlights the benefit of liquid biopsy in select cases and appropriate sample processing for next-generation sequencing.

Conclusions:

  • Implementing best practices in tissue acquisition and processing is vital for improving sample adequacy for NSCLC biomarker testing.
  • Standardizing test availability through improved communication among genomic laboratories and local auditing can further optimize the NSCLC testing pathway.
  • Addressing challenges in the molecular testing pathway will enhance the delivery of personalized medicine for NSCLC patients in the UK.

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