An IHC-derived TLS–CD8–macrophage immune niche score predicts major pathological response to neoadjuvant chemoimmunotherapy in resectable NSCLC - Report - MDSpire
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An IHC-derived TLS–CD8–macrophage immune niche score predicts major pathological response to neoadjuvant chemoimmunotherapy in resectable NSCLC
Clinical Report: Immune Niche Score Predicts Response to Chemoimmunotherapy in NSCLC
Overview
An immune niche score based on immunohistochemistry metrics was developed to predict major pathological response (MPR) in patients with resectable non-small cell lung cancer (NSCLC) undergoing neoadjuvant chemoimmunotherapy. The score demonstrated moderate predictive performance.
Background
Neoadjuvant chemoimmunotherapy has shown promise in improving outcomes for patients with resectable NSCLC, yet responses vary widely among individuals. Current biomarkers, particularly PD-L1 TPS, do not fully capture the complexity of the tumor immune microenvironment.
Data Highlights
Metric
Major Pathological Response (MPR)
Patients Achieving MPR
146 (44.8%)
Patients Achieving Pathological Complete Response
42 (12.9%)
External Validation AUC
0.732 (95% CI, 0.648–0.816)
Key Findings
Higher immune niche scores were associated with MPR in NSCLC patients.
MPR tumors exhibited greater TLS maturity and CD8+ cell proximity to TLS.
Independent predictors of MPR included CD8–TLS proximity (OR 1.68) and CD163/CD68 ratio (OR 0.66).
The composite immune niche score had an OR of 2.72 per 1 SD increase for predicting MPR.
Clinical Implications
Incorporating this score alongside PD-L1 TPS could enhance patient stratification.
Conclusion
The IHC-derived immune niche score predicts MPR in resectable NSCLC and warrants further validation in larger, multicenter studies.