Aug 2026· Cancer Treatment and Research Communications· Vol 49, pp.
101399
· 0 citations· 13 references
Medicine
TL;DR
Laboratory workflow optimization, particularly the adoption of hybrid-capture methodology, significantly improved NGS success rates in a nationwide nsNSCLC testing program, highlighting the need for targeted education and infrastructural investment to broaden equitable access to precision oncology in Brazil.
Abstract
Background
Broad molecular profiling via next-generation sequencing (NGS) is essential for guiding targeted therapy in advanced non-squamous non-small cell lung cancer (nsNSCLC). However, real-world implementation in low- and middle-income countries remains limited by operational challenges.
Methods
We retrospectively analyzed data on nsNSCLC samples tested at a centralized Brazilian genomics laboratory between 2021 and 2025, evaluating NGS performance over time, causes of failure, and the impact of workflow improvements.
Results
A total of 2522 nsNSCLC samples were analyzed between 2021 and 2025. Overall NGS success increased from 64.2% to 85.7% (p < 0.0001) following workflow optimization and the adoption of a hybrid-capture platform with lower DNA input requirement. Insufficient tissue and suboptimal nucleic acid quality were the main causes of failure throughout the study period. Failure rates decreased across all Brazilian regions, although referring laboratories of low volume continued to underperform due to persistent pre-analytical factors.
Conclusion
Laboratory workflow optimization, particularly the adoption of hybrid-capture methodology, significantly improved NGS success rates in a nationwide nsNSCLC testing program. Persistent high failure rates in low-volume centers underscores the need for targeted education and infrastructural investment to broaden equitable access to precision oncology in Brazil.
PURPOSE
Clinical guidelines recommend next-generation sequencing (NGS) before initiation of first-line (1L) therapy as the standard of care for patients with advanced non-small cell lung cancer (aNSCLC). This study examined the impact of timing of molecular testing in relation to treatment initiation on overall surviva...
S. Scott, Danny Nguyen, B. Cai et al.· JCO Precision Oncology· 0 citations
Background: Multigene next-generation sequencing (NGS) has transformed molecular diagnostics in oncology over the past decade, increasingly replaced single-gene approaches such as Sanger sequencing. Although NGS is now integral to precision oncology, differences in laboratory infrastructure, workflow standardization, a...
F. Milanezi, A. Aristizábal, Ariane Falconi et al.· Journal of Experimental and...· 0 citations
INTRODUCTION
For patients with advanced/metastatic non-small cell lung cancer (aNSCLC) without actionable genomic alterations (AGAs) and with programmed death-ligand 1 (PD-L1) ≥ 50%, first-line (1L) treatment options include immunotherapy (IO) monotherapy or IO with chemotherapy. However, real-world data describing tre...
D. Owen, Martin Sebastian, H. Kenmotsu et al.· Oncology and Therapy· 0 citations
The transition from single-gene testing to comprehensive genomic profiling (CGP) is essential for precision oncology. The next generation sequence platform, enables the simultaneous detection of diverse variants and complex immuno-oncology biomarkers, providing a holistic view of the tumor genomic landscape....
Chung-Gue Huang, Shu-Li Yang, Chang-Fu Kuo et al.· Clinical Chemistry· 0 citations
The increasing use of next-generation sequencing (NGS) has revealed substantial molecular heterogeneity in advanced non-small cell lung cancer (NSCLC), yet real-world co-mutation patterns remain incompletely characterized. We aimed to investigate the genomic landscape and clinically relevant co-alteration pattern...
Aysu Sadioğlu, O. Ekinci, Nalan Akyurek· BMC Cancer· 0 citations
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