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Validation of the QR1 Antibody for the Evaluation of PD-L1 Expression in Non-Small Cell Lung Adenocarcinomas

机译:验证非小细胞肺腺癌中PD-L1表达的QR1抗体

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The evaluation of Programmed cell Death Ligand 1 (PD-Ll) expression in the tumor cells with immunohistochemistry is a mandatory diagnostic step in the treatment of lung cancer. It is important to utilize validated antibodies that can reliably detect PD-Ll positive cells. Different antibodies have already been studied. In this present study, we compared a new clone (QR1, Quartett) with reference clones to determine if it can be used in place of previously identified reference clones. We built a tissue micro array (TMA) from 110 lung adenocarcinomas and compared it using im-munohistodetection of four different clones: QR1, 22c3, Sp263, and E1L3N. We analyzed the correlation between the sample duplicates for each clone and then a correlation and the concordance between the clones were calculated. A total of 101 patients were exploitable; the duplicates for each clone had a strong correlation. The correlation was the strongest (r=0.82) between QR1 and 22c3 and less strong with the other clones. Totals of 78%, 79%, and 97% of the QR1 cases were concordant with 22c3 for the thresholds of <1%, 1% to 49%, and > 50%, respectively. The sensitivities and specificities of QR1, compared with 22c3, were > 75% and 81%, respectively. PD-Ll expression, analyzed in lung adenocarcinomas with QR1, is highly correlated and concordant with the main reference clone used in most laboratories (22c3). It can be used to replace the latter in clinical routine.
机译:具有免疫组织化学的肿瘤细胞中程序化细胞死亡配体1(PD-L1)表达的评价是治疗肺癌的强制性诊断步骤。使用可可靠地检测PD-L1阳性细胞的验证抗体是重要的。已经研究了不同的抗体。在本研究中,我们将新的克隆(QR1,Quartett)与参考克隆进行了比较以确定它是否可以用于代替先前识别的参考克隆。我们构建了来自110个肺腺癌的组织微阵列(TMA),并使用四种不同克隆的IM-Munohistodectented进行比较:QR1,22C3,SP263和E1L3N。我们分析了每个克隆的样品复制品之间的相关性,然后计算克隆之间的相关性和克隆之间的一致性。共有101名患者可利用;每个克隆的复制品具有很强的相关性。相关性是QR1和22C3之间的最强(R = 0.82),并且与其他克隆不太强烈。 QR1病例的78%,79%和97%的总体均为22C3,分别为<1%,1%至49%和> 50%的阈值。 QR1的敏感性和特异性分别与22C3相比分别为75%和81%。在具有QR1的肺腺癌中分析的PD-L1表达是高度相关的,并且在大多数实验室(22C3)中使用的主要参考克隆相应。它可用于取代临床常规中的后者。

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