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Using 22C3 Anti-PD-L1 Antibody Concentrate on Biopsy and Cytology Samples from Non-small Cell Lung Cancer Patients
Published on: September 25, 2018
PD-L1 in Cytological Samples: A Review and a Practical Approach
Eva Tejerina1, Laura Garca Tobar2, Jos I Echeveste2
1Department of Pathology, Hospital Universitario Puerta de Hierro, Madrid, Spain.
Immunohistochemistry (IHC) is crucial for predicting immunotherapy response in non-small cell lung cancer (NSCLC). Research is exploring PD-L1 testing feasibility on cytological samples, addressing key challenges for broader application.
Area of Science:
- Oncology
- Pathology
- Biomarker Analysis
Background:
- Non-small cell lung cancer (NSCLC) management increasingly relies on predictive biomarkers.
- Immunohistochemistry (IHC) is a cost-effective method for biomarker testing, particularly for programmed death ligand-1 (PD-L1) in immunotherapy.
- Formalin-fixed paraffin-embedded (FFPE) specimens are standard for PD-L1 assays, but research is expanding to cytological samples.
Purpose of the Study:
- To review the role of cytopathology in analyzing PD-L1 expression for immunotherapy.
- To discuss the feasibility and challenges of using cytological samples for PD-L1 testing.
- To outline future directions for cytopathology in the context of cancer immunotherapy.
Main Methods:
- Literature review summarizing current knowledge on PD-L1 testing in cytopathology.
- Analysis of existing research on immunocytochemistry (ICC) for PD-L1 in NSCLC.
- Identification of key issues in applying PD-L1 assays to cytological specimens.
Main Results:
- IHC is the primary method for PD-L1 assessment in NSCLC, guiding immunotherapy decisions.
- Promising results exist for PD-L1 testing on cytological samples, but standardization is needed.
- Challenges include sample type, pre-analytical variables, cyto-histological correlation, and inter-observer agreement.
Conclusions:
- Cytopathology shows potential for PD-L1 analysis in NSCLC patients undergoing immunotherapy.
- Addressing pre-analytical factors and ensuring reliable cyto-histological correlation are critical for clinical implementation.
- Further research is needed to optimize ICC methods and establish inter-observer agreement for cytological PD-L1 testing.
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