Therapeutic Approaches for Advanced Non-Small Cell Lung Cancer

Summary

Advanced non-small cell lung cancer (NSCLC) encompasses a heterogeneous group of tumours characterised by diverse molecular drivers and histological subtypes. Traditional cytotoxic chemotherapy remains a backbone of treatment but has been progressively supplemented by precision therapies targeting driver mutations in epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK) and other oncogenic kinases. The advent of immune-checkpoint inhibitors directed against programmed cell death-1 (PD-1) or its ligand PD-L1 has transformed clinical outcomes, yielding durable responses in a subset of patients. Antiangiogenic agents that inhibit vascular endothelial growth factor signalling have also been integrated into combination regimens to disrupt tumour vasculature and enhance drug delivery. Despite these advances, therapeutic resistance—both primary and acquired—poses a persistent obstacle, driving exploration of sequential and combination approaches and the identification of predictive biomarkers. Precision oncology relies increasingly on molecular profiling of circulating tumour DNA and extracellular vesicles to guide selection of tyrosine kinase inhibitors, immune-checkpoint blockade and novel agents targeting emerging pathways such as MET amplification or KRAS mutations. Globally, the refinement of multimodal strategies aims to balance efficacy, tolerability and quality of life, extending survival while reducing treatment-related toxicity.

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Therapeutic Approaches for Advanced Non-Small Cell Lung Cancer publication trend

The graph below shows the total number of articles in therapeutic approaches for advanced non-small cell lung cancer across all publications each year (not limited to Nature Index journals).

Technical terms

Non-Small Cell Lung Cancer (NSCLC): A broad category of lung cancers excluding small-cell histology, including adenocarcinoma, squamous cell carcinoma and large-cell carcinoma.

Immune-Checkpoint Inhibitor: A monoclonal antibody that blocks inhibitory immune receptors (such as PD-1 or PD-L1) to enhance anti-tumour T-cell activity.

Tyrosine Kinase Inhibitor (TKI): A small molecule that inhibits phosphorylation of receptor tyrosine kinases involved in tumour proliferation and survival.

Progression-Free Survival (PFS): The length of time during and after treatment in which a patient’s disease does not worsen.

Objective Response Rate (ORR): The proportion of patients with a predefined reduction in tumour burden.

Extracellular Vesicle (EV): A membrane-bound particle released by cells that carries proteins, lipids and nucleic acids and may serve as a biomarker source.

References

  1. Efficacy and safety of immunotherapy combined with single-agent chemotherapy as second- or later-line therapy for metastatic non-small cell lung cancer. Frontiers in Immunology (2023).
  2. Efficacy of Anlotinib Plus Docetaxel in Advanced NSCLC Previously Treated with Platinum-Based Chemotherapy: A Systematic Review and Meta-Analysis. Pharmaceuticals (2025).
  3. Anti-PD-1/PD-L1 antibody therapy for pretreated advanced nonsmall-cell lung cancer. Medicine (2016).

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