Abstract

Immunotherapy has been focused on by many oncologists and researchers. While, due to technical biases of absolute quantification, few traditional biomarkers for anti-PD-1 immunotherapy have been applied in regular clinical practice of non-small cell lung cancer (NSCLC). Therefore, there is an urgent and unmet need for a feasible tool—immune to data source bias—for identifying patients who might benefit from ICIs in clinical practice. Using the strategy based on the relative ranking of gene expression levels, we herein proposed the novel BRGP index (BRGPI): four BRGPs significantly related with progression-free survival of NSCLC patients treated with anti-PD-1 immunotherapy in the multicohort analysis. Moreover, stratification and multivariate Cox regression analyses demonstrated that BRGPI was an independent prognostic factor. Notably, compared to PD-L1, BRGPI exerted the best predictive ability. Further analysis showed that the patients in the BRGPI-low and PD-L1-high subgroup derived more clinical benefits from anti-PD-1 immunotherapy. In conclusion, the prospect of applying the BRGPI to real clinical practice is promising owing to its powerful and reliable predictive value.

Highlights

  • Non-small cell lung cancer (NSCLC) is related with the highest cancer-related mortality worldwide

  • The objective of this study was to construct a predictive signature based on benefit-related gene pairs (BRGPs)—represented by four BRGPs significantly related with progression-free survival (PFS)—

  • Via the multivariate Cox regression, the BRGP index (BRGPI) for each patient was scored based on the following formula [33]: BRGPI score= 1.521 × value of CCL2| vascular endothelial growth factor A (VEGFA) +1.257 × value of cyclin dependent kinase 1 (CDK1)|CXCL9 −1.495 × value of HLADOB|LCK +1.812 × value of interleukin 12A (IL-12A)|T-box 21 (TBX21)

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Summary

Introduction

Non-small cell lung cancer (NSCLC) is related with the highest cancer-related mortality worldwide. It features a high mortality rate and only 19% of those diagnosed with NSCLC will be alive 5 years later [1, 2]. The application of molecular targeted therapy and immunotherapy has allowed many patients to survive longer [3]. Some patients can benefit from targeted molecular therapy, rapid. A Prognostic Signature of Anti-PD-1 Immunotherapy in NSCLC resistance limits its effectiveness in lung cancer treatment [4]. Immune-checkpoint inhibitors (ICIs)—such as pembrolizumab and nivolumab targeting PD-1—have revolutionarily improved the prognosis of patients with NSCLC. Only a small number of patients can derive benefit from ICIs; reliable biomarkers are needed to identify these candidate patients [13]

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