Association of early dynamic changes in peripheral blood immune-inflammatory indices with subsequent acquired resistance to immune checkpoint inhibitors in advanced non-small cell lung cancer: a landmark analysis.
Oct 2026· Immunotherapy· Vol 18, pp.
1-11
· 0 citations· 26 references
Medicine
TL;DR
Early dynamic changes in SII, PNI, and dNLR are associated with subsequent acquired resistance after initial disease control in advanced NSCLC receiving ICI-containing therapy and may support early risk stratification.
Abstract
Background
Acquired resistance to immune checkpoint inhibitors (ICIs) remains a major challenge in advanced non-small cell lung cancer (NSCLC). This study evaluated whether early dynamic changes in peripheral inflammatory and nutritional indices predict subsequent acquired resistance.
Methods
This retrospective landmark cohort included 138 patients with advanced NSCLC who achieved disease control after ICI-containing therapy. Systemic immune-inflammation index (SII), derived neutrophil-to-lymphocyte ratio (dNLR), platelet-to-lymphocyte ratio, prognostic nutritional index (PNI), and lactate dehydrogenase were assessed at baseline and after two ICI cycles. Landmark and time-dependent Cox regression analyses evaluated associations with subsequent progression-free survival (PFS).
Results
During follow-up, 68 patients developed acquired resistance. After adjustment, increased ΔSII (HR = 2.05, 95% CI 1.32-3.18, p = 0.001), decreased ΔPNI (HR = 1.76, 95% CI 1.14-2.71, p = 0.010), and increased ΔdNLR (HR = 1.69, 95% CI 1.10-2.60, p = 0.016) were independently associated with shorter PFS. Time-dependent analyses further confirmed associations of longitudinal SII, PNI, and dNLR trajectories with disease progression.
Conclusions
Early dynamic changes in SII, PNI, and dNLR are associated with subsequent acquired resistance after initial disease control in advanced NSCLC receiving ICI-containing therapy and may support early risk stratification.
Objectives The pan-immune-inflammation value (PIV), calculated from neutrophil, platelet, monocyte, and lymphocyte counts, is a peripheral blood biomarker of systemic immune-inflammatory status. We evaluated the prognostic value of baseline PIV and its trajectory over the first six months of treatment for overall survi...
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Serial flow-cytometric monitoring of CD8⁺ CD28⁺ T cells may represent a promising candidate peripheral biomarker and warrants further investigation in larger cohorts.
A. Garev, N. Gesheva, E. Naumova et al.· Folia Medica· 0 citations
Background Reliable biomarkers for characterization of the risk of severe immune-related adverse events (irAEs) during immune checkpoint inhibition remain lacking. We hypothesized that early dynamics of complementary complete blood count (CBC)-based immune biomarkers may be associated with severe immune toxicity. We th...
O. Fiala, J. Králíček, J. Kopecký et al.· Frontiers in Immunology· 0 citations
Background Immune checkpoint inhibitors (ICIs) have transformed the management of advanced non-small cell lung cancer (NSCLC), but their use is associated with potentially serious immune-related cardiotoxicity, often reflected by elevations in N-terminal pro-B-type natriuretic peptide (NT-proBNP). Identifying patients...
Joanna Ziemska-Legięcka, N. Żeber-Lubecka, Magdalena Borucka et al.· Frontiers in Immunology· 0 citations
Higher IChIS was independently associated with shorter PFS in patients with advanced NSCLC receiving ICIs, supporting its potential role as a simple and readily available prognostic biomarker.
Ismail Dilli, E. E. Kavak, M. Atak et al.· Journal of Clinical Medicine· 0 citations
Background Inflammatory markers have been reported to be associated with outcomes in non-small cell lung cancer (NSCLC). However, whether early treatment-related changes in these markers provide additional prognostic information remains unclear. This study evaluated the association between dynamic changes in peripheral...
Ting-Shan Xu, Zi-Han Wu, Jing-Shan Li et al.· Frontiers in Oncology· 0 citations
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