High-Quality Samples for Next-Generation Sequencing and PD-L1 Assessment in Non-Small Cell Lung Cancer: The Role of

Marta Rodríguez González1, Juan Carlos Montero González1,2, José María Sayagués Manzano1,2

  • 1Department of Pathology, Biomedical Research Institute of Salamanca (IBSAL), University Hospital of Salamanca, 37007 Salamanca, Spain.

Insights

Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) effectively diagnoses non-small cell lung cancer (NSCLC), enabling staging and molecular analysis. This approach optimizes personalized treatment strategies for NSCLC patients.

Area of Science:

  • Pulmonology
  • Oncology
  • Molecular Diagnostics

Background:

  • Advances in non-small cell lung cancer (NSCLC) treatment favor targeted therapies over conventional chemotherapy.
  • Access to targeted therapies is limited by diagnostic challenges in advanced NSCLC, including low cellularity in small biopsies.
  • The growing number of genetic alterations necessitates complex molecular testing.

Purpose of the Study:

  • To evaluate the combined utility of endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) with next-generation sequencing (NGS) and PD-L1 immunohistochemistry.
  • To assess the feasibility of achieving diagnosis, staging, and molecular analysis in a single EBUS-TBNA procedure for NSCLC.

Main Methods:

  • A prospective study involving 120 EBUS-TBNA samples collected over one year.
  • NGS analysis was performed on 67 samples, and PD-L1 determination on 116 samples.
  • Integration of EBUS-TBNA with NGS and PD-L1 testing at a reference hospital.

Main Results:

  • The EBUS-TBNA procedure successfully met the National Comprehensive Cancer Network (NCCN) triple objective (diagnosis, staging, molecular analysis) in 97% of cases.
  • High-quality samples suitable for NGS and PD-L1 testing were consistently obtained.
  • The diagnostic approach demonstrated high effectiveness with minimal complications.

Conclusions:

  • EBUS-TBNA is a comprehensive, cost-effective, and safe diagnostic tool for NSCLC.
  • The procedure reliably facilitates diagnosis, staging, and molecular profiling in a single intervention.
  • This integrated approach optimizes personalized treatment strategies for NSCLC patients.