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Comparable immunoreactivity rates of PD‐L1 in archival and recent specimens from non‐small cell lung cancer

机译:非小细胞肺癌档案和近期样本中PD-L1的免疫反应率相当

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Background Molecular targeted therapy including the use of monoclonal antibodies directed against the immune checkpoints PD‐L1 and PD‐1 receptor have remarkably improved the therapeutic response and survival of cancer patients. The tumor expression level of PD‐L1 can predict the response rate to checkpoint inhibitors. We evaluated whether the time interval between tumor tissue sampling/paraffinization and immunohistochemistry affects the staining level of PD‐L1 in non‐small cell lung cancer (NSCLC). Methods This study comprised 137 patients with NSCLC. Tumors were stained with 22C3 or 28‐8 antibodies. Results There was a significant correlation between the immunoreactivity rate of tumor tissues obtained using 22C3 and 28‐8 clones. No statistical difference in immunoreactivity between archival and recent samples stained either with 22C3 or 28‐8 antibodies was observed. The immunoreactivity rate achieved with 22C3 or 28‐8 antibodies significantly correlated with tumor histological type and size, but not with specimen storage time, age, gender, smoking history, clinical stage, or lymph node metastasis. Conclusion In brief, the results of this study show that the time interval between tissue sampling/paraffinization and immunohistochemical analysis has no influence on the immunoreactivity rate of PD‐L1 in NSCLC.
机译:背景技术分子靶向疗法包括使用针对免疫检查点PD-1和PD-1受体的单克隆抗体,显着改善了癌症患者的治疗反应和生存率。 PD-L1的肿瘤表达水平可以预测对检查点抑制剂的反应率。我们评估了肿瘤组织采样/石蜡化与免疫组织化学之间的时间间隔是否会影响非小细胞肺癌(NSCLC)中PD-L1的染色水平。方法这项研究包括137例NSCLC患者。肿瘤用22C3或28-8抗体染色。结果使用22C3和28-8克隆获得的肿瘤组织的免疫反应率之间存在显着相关性。档案和最近用22C3或28-8抗体染色的样本之间的免疫反应性均无统计学差异。使用22C3或28-8抗体获得的免疫反应率与肿瘤的组织学类型和大小显着相关,但与标本的存储时间,年龄,性别,吸烟史,临床分期或淋巴结转移无关。结论简而言之,这项研究的结果表明,组织取样/石蜡化与免疫组织化学分析之间的时间间隔对NSCLC中PD-L1的免疫反应率没有影响。

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