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首页> 外文期刊>The British journal of cancer >Clinical implications of heterogeneity in PD-L1 immunohistochemical detection in hepatocellular carcinoma: the Blueprint-HCC study
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Clinical implications of heterogeneity in PD-L1 immunohistochemical detection in hepatocellular carcinoma: the Blueprint-HCC study

机译:异质性在PD-L1免疫组织化学检测中的临床意义:肝细胞癌:蓝图-HCC研究

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摘要

Programmed cell death ligand-1 immunohistochemical detection (PD-L1 IHC) is a putative predictor of response to PD-1/PD-L1targeted checkpoint inhibitors. However, there is no gold standard assay in hepatocellular carcinoma (HCC). We evaluated 5 PD-L1 IHC assay platforms (E1LN3, 28-8, 22c3, SP263 and SP142) in 100 HCCs reporting PD-L1 expression in malignant (M) and tumourinfiltrating immune cells (TICs) and non-tumorous cirrhotic tissues (NTICs). We found substantial inter-assay heterogeneity in detecting PD-L1 expression in M (R-2 = 0.080-0.921), TICs (Cohen's kappa = 0.175-0.396) and NTICs (kappa = 0.004-0.505). Such diversity may impact on the reliability and reproducibility of PD-L1 IHC assays as a predictor of response to immune checkpoint inhibitors.
机译:程序性细胞死亡配体1免疫组织化学检测(PD-L1 IHC)是对PD-1/PD-L1TARGETED检查点抑制剂的反应的假定预测指标。 但是,肝细胞癌(HCC)中没有黄金标准测定法。 我们在100个HCC中评估了5个PD-L1 IHC测定平台(E1LN3、28-8、22C3,SP263和SP142),在100个HCCS中报告了恶性(M)和肿瘤氟免疫细胞(TICS)和非肿瘤性CirrHotic Tiscues(NTICS)中PD-L1的表达(NTICS)(NTICS) )。 我们发现在M(R-2 = 0.080-0.921)中检测PD-L1表达时,发现了实质性的异质性。 这种多样性可能会影响PD-L1 IHC分析的可靠性和可重复性,以预测对免疫检查点抑制剂的反应。

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