Analysis of blood-derived ctDNA identifies genomic markers in advanced NSCLC, suggesting improved immunotherapy outcomes.
Predictive biomarkers for immune checkpoint inhibitors (ICIs) in advanced NSCLC remain imperfect. While blood-based tumour mutational burden (bTMB) is attractive, its performance is inconsistent. Whole-exome sequencing (WES) of plasma-derived ctDNA, analysed through an automated, AI-enabled platform (AIRGenomics), may reveal broader genomic patterns associated with response or resistance to immunotherapy.
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Posado-Domínguez et al. (2026) studied this question.
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