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Updated: Jan 19, 2026

Identifying PD-1/PD-L1 Inhibitors with Surface Plasmon Resonance Technology
Published on: May 2, 2025
[Predictive diagnostics of the programmed cell death receptor 1 (PD-1) - programmed cell death ligand 1 (PD-L1)
Gábor Lotz1, Gábor Smuk2, Éva Kocsmár1
1II. Sz. Patológiai Intézet, Semmelweis Egyetem, Budapest, Hungary. lotz.gabor@med.semmelweis-univ.hu.
Abstract:
In the past years, immunotherapy emerged as a novel modality of clinical oncology. The development and introduction of immune checkpoint inhibitors required the development of companion diagnostics, the PD-L1 protein immunohistochemical tests. Unfortunately, almost all checkpoint inhibitors were exclusively validated by a specific PD-L1 in vitro diagnostic test with its own evaluation protocol. These tests have different diagnostic sensitivity for PD-L1 protein and the evaluation protocols differ in many respects, as cancer and immune cell positivities are considered variously in the immunotherapy-specific evaluation schemes. Accordingly, in the routine PD-L1 diagnostics, it is crucial to follow the individual therapy-specific technical and evaluation protocols since these are not interchangeable and non-adherence may affect therapeutic efficacy.
Insights
Immuno-oncology uses companion diagnostics like PD-L1 tests. Adhering to specific test protocols is crucial for effective immunotherapy treatment, as these tests are not interchangeable.
Area of Science:
- Oncology
- Immunology
- Diagnostics
Background:
- Immunotherapy has revolutionized cancer treatment.
- Immune checkpoint inhibitors (ICIs) require companion diagnostics.
- PD-L1 protein immunohistochemical tests are key companion diagnostics for ICIs.
Purpose of the Study:
- To highlight the importance of specific PD-L1 testing protocols.
- To emphasize the non-interchangeability of different PD-L1 assays.
- To underscore the impact of protocol adherence on immunotherapy efficacy.
Main Methods:
- Review of PD-L1 testing validation for immune checkpoint inhibitors.
- Analysis of variations in PD-L1 diagnostic sensitivity and evaluation protocols.
- Comparison of cancer and immune cell positivity assessments across different schemes.
Main Results:
- Most ICIs are validated with specific, non-interchangeable PD-L1 tests.
- PD-L1 tests exhibit varying diagnostic sensitivity.
- Evaluation protocols differ significantly in assessing PD-L1 expression.
Conclusions:
- Routine PD-L1 diagnostics demand strict adherence to therapy-specific protocols.
- Non-adherence to individual test protocols can compromise therapeutic efficacy.
- Standardization and careful protocol selection are vital for successful immunotherapy.
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