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Biomarkers for Predicting Efficacies of Anti-PD1 Antibodies
Yumi Kambayashi1, Taku Fujimura1, Takanori Hidaka1
1Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Abstract:
Therapeutic options for treating advanced melanoma are progressing rapidly. Although anti-programmed cell death 1 (PD1) antibodies (e.g., nivolumab, pembrolizumab) have been approved as first-line and anchor drugs, respectively, for treating advanced melanoma, the efficacy appears limited as we expected, especially in Asian populations. Biomarkers to predict or evaluate the efficacy of anti-PD1 antibodies are needed to avoid subjecting patients to potentially severe adverse events associated with switching to other anti-melanoma drugs. This review focuses on the recent development of biomarkers for assessing the efficacy of anti-PD1 antibodies using routine blood tests such as the neutrophil-to-lymphocyte ratio, eosinophil ratio, serum markers such as lactate dehydrogenase, programmed cell death ligand 1 (PD-L1) expression on melanoma cells, microsatellite instability and mismatch repair deficiency assays, as well as soluble CD163, and tumor-associated macrophage-related chemokines (e.g., CXCL5, CXCL10).
Insights
Predicting advanced melanoma treatment response is crucial. This review explores biomarkers, including blood tests and PD-L1 expression, to assess anti-programmed cell death 1 (PD1) antibody efficacy, aiding treatment decisions.
Area of Science:
- Oncology
- Immunotherapy
- Biomarker Discovery
Background:
- Advanced melanoma treatment is rapidly evolving with anti-programmed cell death 1 (PD1) antibodies.
- Current therapies show limited efficacy, particularly in Asian populations.
- Predictive biomarkers are essential to guide treatment and mitigate adverse events.
Purpose of the Study:
- To review recent developments in biomarkers for assessing anti-PD1 antibody efficacy in advanced melanoma.
- To identify potential biomarkers detectable through routine blood tests and tumor analysis.
Main Methods:
- Literature review of studies on biomarkers for anti-PD1 therapy response.
- Analysis of various biomarkers including neutrophil-to-lymphocyte ratio, eosinophil ratio, lactate dehydrogenase, PD-L1 expression, microsatellite instability, mismatch repair deficiency, soluble CD163, and chemokines (CXCL5, CXCL10).
Main Results:
- Several biomarkers show promise in predicting or evaluating anti-PD1 antibody efficacy.
- Routine blood tests and PD-L1 expression are key areas of investigation.
- Tumor-based assays like MSI and dMMR also play a role.
Conclusions:
- Developing reliable biomarkers is critical for optimizing advanced melanoma treatment with anti-PD1 antibodies.
- Further research is needed to validate these biomarkers for clinical application.
- Biomarker-guided therapy can improve patient outcomes and reduce unnecessary toxicity.
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