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Updated: Feb 6, 2026

Identifying PD-1/PD-L1 Inhibitors with Surface Plasmon Resonance Technology
Published on: May 2, 2025
Targeting the PD-1/PD-L1 axis for the treatment of non-small-cell lung cancer
D E Meyers1,2, P M Bryan1, S Banerji3,4
1Department of Oncology, University of Calgary, and.
Abstract:
Lung cancer is the leading cause of cancer-specific death among Canadians, with non-small-cell lung cancer (nsclc) being the most common histologic variant. Despite advances in the understanding of the molecular biology of nsclc, the survival rate for this malignancy is still poor. It is now understood that, to evade detection and immune clearance, nsclc tumours overexpress the immunosuppressive checkpoint protein programmed death ligand 1 (PD-L1). Inhibiting the PD-1/PD-L1 axis with monoclonal antibodies has significantly changed the treatment landscape in nsclc during the last 5 years. Despite evidence of clinical response in some patients, only approximately 20% of patients obtain any durable benefit, and many of the patients who do respond ultimately relapse with drug-resistant disease. The identification of patients who are most likely to benefit from such therapy is therefore important. In the present review, we cover the basics of the PD-1/PD-L1 axis and its clinical significance in nsclc, biomarkers that are predictive of treatment response, relevant clinical trials of PD-1/PD-L1 blockade completed to date, and proposed mechanisms of acquired therapeutic resistance.
Insights
Non-small-cell lung cancer (NSCLC) treatments targeting the PD-1/PD-L1 axis show limited durable benefit. Identifying predictive biomarkers is crucial for selecting patients likely to respond to immunotherapy and overcome resistance.
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- Non-small-cell lung cancer (NSCLC) is a leading cause of cancer death.
- Despite advances, NSCLC survival rates remain poor.
- NSCLC tumors overexpress PD-L1 to evade immune detection.
Purpose of the Study:
- Review the PD-1/PD-L1 axis in NSCLC.
- Discuss biomarkers for predicting treatment response.
- Explore mechanisms of acquired resistance to PD-1/PD-L1 blockade.
Main Methods:
- Literature review of PD-1/PD-L1 axis in NSCLC.
- Analysis of clinical trials involving PD-1/PD-L1 inhibitors.
- Synthesis of data on predictive biomarkers and resistance mechanisms.
Main Results:
- PD-1/PD-L1 blockade has changed NSCLC treatment but benefits only ~20% of patients.
- Durable responses are limited, with many patients relapsing due to resistance.
- Biomarker identification is critical for patient selection.
Conclusions:
- Targeting the PD-1/PD-L1 axis offers therapeutic potential in NSCLC.
- Predictive biomarkers are essential for optimizing immunotherapy efficacy.
- Understanding resistance mechanisms is key to improving patient outcomes.
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