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Background <p>The efficacy of single-agent immune checkpoint inhibitors as a first-line treatment for advanced non-small cell lung cancer (aNSCLC) patients with PD-L1 Tumor Proportion Score (TPS) &lt; 50% remains variable. Network analysis is promising in addressing tumor biology and behavior, potentially predicting therapeutic response.</p> Methods <p>This study, based on the PEOPLE trial (NCT03447678) data, explores network analysis for predictive biomarker discovery in immunotherapy response. Utilizing circulating immune profiling (CIP) and gene expression profiling (GEP), key immune cells and gene interactions were identified.</p> Results <p>Our findings confirm the central role of natural killer (NK) cells, with elevated baseline levels associated with a favorable response. Differential co-expression network (DCN) analysis of GEP identified 23 hub genes, with enrichment analysis linking CD48 to immune-related processes. Patient similarity network (PSN) analysis identified two patient clusters with significantly different survival outcomes. The integrated model outperformed single-layer approaches, supporting the added value of combining GEP and CIP data.</p> Conclusions <p>Despite limitations such as a non-randomized design and small sample size, the study’s innovative network approach provides valuable insights. The results suggest that baseline NK cell subsets and specific gene evaluations could guide personalized treatment strategies, optimizing the use of pembrolizumab in aNSCLC patients with PD-L1 TPS &lt; 50%.</p>

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Network analysis predicts pembrolizumab response in advanced NSCLC with PD-L1 < 50%

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年3月26日

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  • Mario Occhipinti,
  • Antonella Cruoglio,
  • Silvia Marchesi,
  • Arsela Prelaj,
  • Marco Petrilli,
  • Aurelia Rughetti,
  • Paolo Ambrosini,
  • Elisabetta Ferretti,
  • Claudia Proto,
  • Monica Ganzinelli,
  • Marta Brambilla,
  • Laura Mazzeo,
  • Teresa Beninato,
  • Filippo de Braud,
  • Marina Chiara Garassino,
  • Lorenzo Farina,
  • Giuseppe Lo Russo,
  • Manuela Petti

摘要

Background

The efficacy of single-agent immune checkpoint inhibitors as a first-line treatment for advanced non-small cell lung cancer (aNSCLC) patients with PD-L1 Tumor Proportion Score (TPS) < 50% remains variable. Network analysis is promising in addressing tumor biology and behavior, potentially predicting therapeutic response.

Methods

This study, based on the PEOPLE trial (NCT03447678) data, explores network analysis for predictive biomarker discovery in immunotherapy response. Utilizing circulating immune profiling (CIP) and gene expression profiling (GEP), key immune cells and gene interactions were identified.

Results

Our findings confirm the central role of natural killer (NK) cells, with elevated baseline levels associated with a favorable response. Differential co-expression network (DCN) analysis of GEP identified 23 hub genes, with enrichment analysis linking CD48 to immune-related processes. Patient similarity network (PSN) analysis identified two patient clusters with significantly different survival outcomes. The integrated model outperformed single-layer approaches, supporting the added value of combining GEP and CIP data.

Conclusions

Despite limitations such as a non-randomized design and small sample size, the study’s innovative network approach provides valuable insights. The results suggest that baseline NK cell subsets and specific gene evaluations could guide personalized treatment strategies, optimizing the use of pembrolizumab in aNSCLC patients with PD-L1 TPS < 50%.