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Author Spotlight: Advancements in Molecular Biomarker Testing for Non-Squamous Non-Small Cell Lung Cancer
Published on: September 8, 2023
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.
Abstract:
Targeted therapy against actionable variants has revolutionised the treatment landscape for non-small cell lung cancer (NSCLC). Approximately half of NSCLC adenocarcinomas have an actionable variant, making molecular testing a critical component of the diagnostic process to personalise therapeutic options, optimise clinical outcomes and minimise toxicity. Recently, genomic testing in England has undergone major changes with the introduction of Genomic Laboratory Hubs, designed to consolidate and enhance existing laboratory provision and deliver genomic testing as outlined in the National Genomic Test Directory. Similar changes are ongoing in Scotland, Wales and Northern Ireland. However, multiple challenges exist with current tissue acquisition procedures and the molecular testing pathway in the UK, including quantity and quality of available tissue, adequacy rates, test availability among genomic laboratories, turnaround times, multidisciplinary team communication, and limited guidance and standardisation. The COVID-19 pandemic has added an extra layer of complexity. Herein, we summarise best practice recommendations, based on expert opinion, to overcome existing challenges in the UK. The least invasive biopsy technique should be undertaken with the aim of acquiring the greatest quality and quantity of tissue. Use of sedation should be considered to improve patient experience. Rapid on-site evaluation may also be useful to help guide adequate sampling, and liquid biopsy may be beneficial in some instances. Sample processing should be appropriate to facilitate biomarker testing, in particular, next-generation sequencing for comprehensive genomic information. Steps to optimise tissue utilisation and turnaround times, such as planning of tissue usage, limiting immunohistochemistry, tumour enrichment, and reflex testing at diagnosis, should be implemented. Guidelines for tissue acquisition and sample processing may help to improve sample adequacy to perform downstream testing. Communication among genomic laboratories will help to standardise test availability across England and local auditing could identify further areas for optimisation, including ways to improve turnaround times and adequacy rates.
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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