Røge Rasmus, Vyberg Mogens, Nielsen Søren
*Institute of Pathology, Aalborg University Hospital †Department of Clinical Medicine, Aalborg University, Aalborg Denmark.
Appl Immunohistochem Mol Morphol. 2017 Jul;25(6):381-385. doi: 10.1097/PAI.0000000000000534.
Treatment using immunotherapy against PD-L1 or PD-1 has become one of the hottest topics in Pathology and Oncology. Correct selection of patients eligible for treatment requires optimal immunohistochemical staining protocols. Treatment with pembrolizumab requires diagnostic examination of the patient's tumour using the companion diagnostic Ready-To-Use pharmDx kit from Dako Agilent based on the mAb 22C3 clone on the Autostainer platform. However, not all diagnostic pathology labs have access to this staining platform. This purpose of this study was to develop and validate protocols for PD-L1 detection for all major staining platforms using the concentrated format of 22C3 that would give similar staining result (equal Tumour Proportion Scores) to the pharmDx kit.
使用针对PD-L1或PD-1的免疫疗法进行治疗已成为病理学和肿瘤学领域最热门的话题之一。正确选择适合治疗的患者需要优化的免疫组织化学染色方案。使用派姆单抗进行治疗需要使用达科安捷伦公司基于单克隆抗体22C3克隆的即用型伴随诊断试剂pharmDx试剂盒,在自动染色平台上对患者的肿瘤进行诊断检查。然而,并非所有诊断病理实验室都能使用这种染色平台。本研究的目的是开发并验证使用浓缩型22C3针对所有主要染色平台进行PD-L1检测的方案,该方案将产生与pharmDx试剂盒相似的染色结果(相同的肿瘤比例评分)。