Related Experiment Video
Updated: Nov 2, 2025

Author Spotlight: Advancements in Molecular Biomarker Testing for Non-Squamous Non-Small Cell Lung Cancer
Published on: September 8, 2023
Cost-effectiveness of precision diagnostic testing for precision medicine approaches against non-small-cell lung
Raymond Henderson1, Peter Keeling1, Declan French2
1Diaceutics PLC, Belfast, UK.
Abstract:
Precision diagnostic testing (PDT) employs appropriate biomarkers to identify cancer patients that may optimally respond to precision medicine (PM) approaches, such as treatments with targeted agents and immuno-oncology drugs. To date, there are no published systematic appraisals evaluating the cost-effectiveness of PDT in non-small-cell lung cancer (NSCLC). To address this gap, we conducted Preferred Reporting Items for Systematic Reviews and Meta-Analyses searches for the years 2009-2019. Consolidated Health Economic Evaluation Reporting Standards were employed to screen, assess and extract data. Employing base costs, life years gained or quality-adjusted life years, as well as willingness-to-pay (WTP) threshold for each country, net monetary benefit was calculated to determine cost-effectiveness of each intervention. Thirty-seven studies (50%) were included for analysis; a further 37 (50%) were excluded, having failed population-, intervention-, comparator-, outcomes- and study-design criteria. Within the 37 studies included, we defined 64 scenarios. Eleven scenarios compared PDT-guided PM with non-guided therapy [epidermal growth factor receptor (EGFR), n = 5; programmed death-ligand 1 (PD-L1), n = 6]. Twenty-eight scenarios compared PDT-guided PM with chemotherapy alone (anaplastic lymphoma kinase, n = 3; EGFR, n = 17; PD-L1, n = 8). Twenty-five scenarios compared PDT-guided PM with chemotherapy alone, while varying the PDT approach. Thirty-four scenarios (53%) were cost-effective, 28 (44%) were not cost-effective, and two were marginal, dependent on their country's WTP threshold. When PDT-guided therapy was compared with a therapy-for-all patients approach, all scenarios (100%) proved cost-effective. Seven of 37 studies had been structured appropriately to assess PDT-PM cost-effectiveness. Within these seven studies, all evaluated scenarios were cost-effective. However, 81% of studies had been poorly designed. Our systematic analysis implies that more robust health economic evaluation could help identify additional approaches towards PDT cost-effectiveness, underpinning value-based care and enhanced outcomes for patients with NSCLC.
Insights
Precision diagnostic testing (PDT) for non-small-cell lung cancer (NSCLC) is cost-effective when guiding precision medicine (PM) compared to a one-size-fits-all approach. However, many studies had poor design, limiting robust economic evaluation.
Area of Science:
- Oncology
- Health Economics
- Biomarker Discovery
Background:
- Precision diagnostic testing (PDT) identifies patients likely to benefit from precision medicine (PM) in non-small-cell lung cancer (NSCLC).
- Cost-effectiveness evaluations of PDT in NSCLC are lacking.
- Systematic reviews and meta-analyses are crucial for assessing healthcare interventions.
Purpose of the Study:
- To systematically evaluate the cost-effectiveness of precision diagnostic testing (PDT) in non-small-cell lung cancer (NSCLC).
- To identify factors influencing the cost-effectiveness of PDT-guided precision medicine (PM).
- To address the gap in published economic appraisals for PDT in NSCLC.
Main Methods:
- Conducted systematic searches (2009-2019) using Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines.
- Applied Consolidated Health Economic Evaluation Reporting Standards (CHEERS) for data screening and extraction.
- Calculated net monetary benefit using cost, quality-adjusted life years, and country-specific willingness-to-pay thresholds.
Main Results:
- 37 studies were included, defining 64 cost-effectiveness scenarios.
- 53% of scenarios were cost-effective, 44% were not, and 2% were marginal.
- PDT-guided therapy compared to a universal approach was 100% cost-effective.
- Only 7 of 37 studies were appropriately designed for cost-effectiveness assessment; all their scenarios were cost-effective.
- 81% of studies exhibited poor design, impacting the reliability of their economic evaluations.
Conclusions:
- PDT-guided precision medicine (PM) demonstrates cost-effectiveness in NSCLC, particularly when compared to non-selective treatment strategies.
- Robust health economic evaluations are essential for optimizing PDT cost-effectiveness and supporting value-based care in NSCLC.
- Improving study design in health economic evaluations is critical for reliable assessment of PDT-PM interventions.
More Related Videos
13:24Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies
Published on: April 11, 2016
08:14MicroRNA Based Liquid Biopsy: The Experience of the Plasma miRNA Signature Classifier MSC for Lung Cancer Screening
Published on: October 26, 2017