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原发性和转移性膀胱癌中 PD-L1 表达的一致性研究:四种常用抗体和 RNA 表达的比较。

Concordance study of PD-L1 expression in primary and metastatic bladder carcinomas: comparison of four commonly used antibodies and RNA expression.

机构信息

Department of Pathology, University of Washington Medical Center, Seattle, WA, USA.

PhenoPath Laboratories, Seattle, WA, USA.

出版信息

Mod Pathol. 2018 Apr;31(4):623-632. doi: 10.1038/modpathol.2017.188. Epub 2017 Dec 22.

Abstract

Therapy with anti-PD-L1 immune check-point inhibitors is approved for several cancers, including advanced urothelial carcinomas. PD-L1 prevalence estimates vary widely in bladder cancer, and lack of correlation between expression and clinical outcomes and immunotherapy response may be attributed to methodological differences of the immunohistochemical reagents and procedures. We characterized PD-L1 expression in 235 urothelial carcinomas including 79 matched pairs of primary and metastatic cancers using a panel of four PD-L1 immunoassays in comparison with RNAscope assay using PD-L1-specific probe (CD274). The antibody panel included three FDA-approved clones (22C3 for pembrolizumab, 28.8 for nivolumab, SP142 for atezolizumab), and a commonly used clone E1L3N. Manual scoring of tissue microarrays was performed in each of 235 tumors (624 tissue cores) and compared to an automated image analysis. Expression of PD-L1 in tumor cells by ≥1 marker was detected in 41/142 (28.9%) primary tumors, 13/77 (16.9%) lymph nodes, and 2/16 (12.5%) distant metastases. In positive cases, high PD-L1 expression (>50% cells) was detected in 34.1% primary and 46.7% metastases. Concordant PD-L1 expression status was present in 71/79 (89.9%) cases of matched primary and metastatic urothelial carcinomas. PD-L1 sensitivity ranked from highest to lowest as follows: RNAscope, clone 28.8, 22C3, E1L3N, and SP142. Pairwise concordance correlation coefficients between the four antibodies in 624 tissue cores ranged from 0.76 to 0.9 for tumor cells and from 0.30 to 0.85 for immune cells. RNA and protein expression levels showed moderate to high agreement (0.72-0.87). Intra-tumor expression heterogeneity was low for both protein and RNA assays (interclass correlation coefficients: 0.86-0.94). Manual scores were highly concordant with automated Aperio scores (0.94-0.97). A significant subset of 56/235 (23.8%) urothelial carcinomas stained positive for PD-L1 with high concordance between all four antibodies and RNA ISH assay. Despite some heterogeneity in staining, the overall results are highly concordant suggesting diagnostic equivalence of tested assays.

摘要

抗 PD-L1 免疫检查点抑制剂的治疗已被批准用于多种癌症,包括晚期尿路上皮癌。在膀胱癌中,PD-L1 的流行率估计差异很大,表达与临床结果和免疫治疗反应之间缺乏相关性,可能归因于免疫组织化学试剂和程序的方法学差异。我们使用四种 PD-L1 免疫测定法的面板,比较了使用 PD-L1 特异性探针 (CD274) 的 RNAscope 测定法,对 235 例尿路上皮癌包括 79 对原发性和转移性癌症进行了 PD-L1 表达特征分析。抗体面板包括三种 FDA 批准的克隆物(用于 pembrolizumab 的 22C3、用于 nivolumab 的 28.8、用于 atezolizumab 的 SP142)和一种常用的克隆物 E1L3N。对 235 个肿瘤中的每个肿瘤(624 个组织芯)进行了组织微阵列的手动评分,并与自动图像分析进行了比较。在 142 个原发性肿瘤中检测到≥1 种标记物的 PD-L1 在肿瘤细胞中的表达为 41/142(28.9%),在 77 个淋巴结中为 13/77(16.9%),在 16 个远处转移中为 2/16(12.5%)。在阳性病例中,在 34.1%的原发性肿瘤和 46.7%的转移瘤中检测到高 PD-L1 表达(>50%的细胞)。79 对匹配的原发性和转移性尿路上皮癌中,有 71/79(89.9%)存在 PD-L1 表达状态一致。PD-L1 敏感性从高到低依次为:RNAscope、克隆 28.8、22C3、E1L3N 和 SP142。四种抗体在 624 个组织芯中的两两一致性相关系数在肿瘤细胞中为 0.76-0.9,在免疫细胞中为 0.30-0.85。RNA 和蛋白质表达水平具有中度至高度一致性(0.72-0.87)。无论是蛋白质还是 RNA 检测,肿瘤内表达异质性均较低(组内相关系数:0.86-0.94)。手动评分与自动 Aperio 评分高度一致(0.94-0.97)。有 56/235(23.8%)例尿路上皮癌用四种抗体和 RNA ISH 检测均呈 PD-L1 阳性,且具有高一致性,提示检测方法具有诊断等效性。尽管存在一些染色异质性,但总体结果高度一致,表明测试的方法具有诊断等效性。

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