# Lung cancer immunotherapy in 2025: where we stand and what comes next?

**Authors:** Jie Han, Zhibo Yang, Hai Zhao

PMC · DOI: 10.3389/fimmu.2025.1728163 · 2026-01-16

## TL;DR

This review discusses the progress and future directions of immunotherapy for lung cancer, focusing on improving patient outcomes through new strategies and biomarkers.

## Contribution

The paper provides a comprehensive overview of current and emerging immunotherapies for lung cancer, emphasizing stage-specific and biomarker-driven approaches.

## Key findings

- Immune checkpoint inhibitors have improved outcomes in various stages of lung cancer.
- Only a fraction of patients benefit from immunotherapy due to resistance and other challenges.
- Emerging therapies like CAR-T and vaccines are being explored to enhance treatment effectiveness.

## Abstract

Lung cancer continues to be the leading cause of cancer-related mortality worldwide, accounting for more deaths than breast, colorectal, and prostate cancers combined. Over the past decade, the introduction of immunotherapy has reshaped treatment paradigms, offering hope for long-term survival in a disease historically associated with dismal outcomes. The incorporation of immune checkpoint inhibitors (ICIs) into the treatment of non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) has improved outcomes across early-stage, locally advanced, and metastatic settings. However, only a fraction of patients derive durable benefit, and challenges remain in overcoming resistance, predicting response, managing toxicity, and ensuring equitable access. This review provides a comprehensive overview of current progress in lung cancer immunotherapy. It discusses the immunobiology of lung tumors, the role of checkpoint blockade across disease stages, mechanisms of resistance, biomarker development, and combination strategies. Emerging modalities, including bispecific antibodies, CAR- and TCR-based cellular therapies, natural killer (NK) cell platforms, cytokine agonists, oncolytic viruses, and vaccines, are explored in depth. We also evaluate the translational significance of preclinical models, toxicity management, and issues of equity and accessibility. Finally, we outline key future directions that may redefine lung cancer immunotherapy in the coming years. Collectively, these advances highlight a transition from broad applications of checkpoint inhibition toward stage-specific, biomarker-driven, and multimodal immunotherapy approaches designed to convert temporary responses into durable remissions and, ultimately, cures.

## Linked entities

- **Diseases:** lung cancer (MONDO:0005138), non-small cell lung cancer (MONDO:0005233), small cell lung cancer (MONDO:0008433)

## Full-text entities

- **Genes:** CXADRP1 (CXADR pseudogene 1) [NCBI Gene 653108] {aka CAR, CXADRP}, TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}
- **Diseases:** breast, colorectal, and prostate cancers (MESH:D001943), SCLC (MESH:D055752), NSCLC (MESH:D002289), Lung cancer (MESH:D008175), cancer (MESH:D009369), toxicity (MESH:D064420)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12855455/full.md

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Source: https://tomesphere.com/paper/PMC12855455