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Establishing the Economic Value of Carbon-Minimal Inhalers
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Next-generation sequencing (NGS) generates comprehensive and actionable information on molecular tumour profiles. But despite recommendations for the use of NGS in lung cancer, and support for its clinical value, access is variable across Europe.
This report explores the status of access and uptake for NGS testing for lung cancer in Europe. We develop the health economic case for NGS testing and identify barriers and opportunities for widespread access to NGS testing for patients with lung cancer in Europe.
We found a wealth of evidence supporting the clinical value of NGS testing in lung cancer, with broad agreement on the mechanisms by which it can improve patient outcomes. Evidence also demonstrates the potential for efficiency and cost savings arising from the use of NGS testing. In addition to clinical and economic benefits, genomic testing is associated with broader elements of value, especially the ‘value of knowing’.
Whilst the prevailing barriers and opportunities differ across countries, we have specified three generalisable objectives and policy initiatives that can facilitate progress and increase uptake:
We elaborate these in a set of six actionable recommendations for decision-makers which are detailed in the full report and summarised in Figure 1 below.
Figure 1: The pathway to improved uptake of NGS for lung cancer in Europe
The Case for Expanding Uptake of Next-Generation Sequencing for Lung Cancer in Europe