Abstract

The immune checkpoint inhibitors against programmed death 1 (PD1) or its ligand (PD-L1) has demonstrated significant efficacy in multiple cancer types. Thus, selecting patients most likely to respond to these therapies is necessary. PD-L1 expression by immunohistochemistry has been proposed as a potential predictive biomarker of response. A statistically significant difference in Overall Response Rate (ORR) between PD-L1 positive and PD-L1 negative tumors has been reported. However, there is not a common reference standard for PD-L1 quantification.

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