Department of Pathology, Medical University of Vienna, Wien, Austria.
Comprehensive Cancer Center Vienna, Upper GI Tumors Unit, Medical University of Vienna, Wien, Austria.
Pathol Oncol Res. 2020 Oct;26(4):2225-2235. doi: 10.1007/s12253-020-00814-2. Epub 2020 May 5.
Immunotherapy with check-point inhibitors serves as a promising treatment strategy in patients with upper gastrointestinal (GI) tumors. Human epidermal growth factor receptor 2 (HER2) is the only identified therapeutic target in upper GI tumors, whose potential interaction with programmed death-ligand 1 (PD-L1) is unknown. The aim of this study was the investigation of PD-L1 and HER2 in upper GI tumors. We retrospectively identified patients with HER2 positive gastroesophageal cancers and matched them with a HER2 negative group. We investigated the tumor specimens for HER2 status and PD-L1 expression, with the following assessments being performed: i) staining of tumor cells in terms of tumor proportion score (TPS), ii) staining for tumor-associated immune cells (TAIs), iii) interface pattern and iv) combined positive score (CPS). Both HER2 positive and negative group consisted of 59 patients. Expression of PD-L1 in TAIs and interface pattern were associated with a favorable outcome (p = 0.02, HR = 0.8; p = 0.04, HR = 0.39; respectively) in patients with localized disease, whereas TPS was associated with an unfavorable outcome in patients with advanced tumor (p = 0.02, HR = 1.4). These effects were HER2 independent. PD-L1 expression in its different assessment is equally observed in HER2 positive and negative patients. Future studies will show whether dual inhibition of HER2 and PD-L1 improves survival of this selected patient population.
免疫检查点抑制剂治疗在消化道(GI)肿瘤患者中具有广阔的应用前景。人表皮生长因子受体 2(HER2)是上消化道肿瘤中唯一被识别的治疗靶点,其与程序性死亡配体 1(PD-L1)的潜在相互作用尚不清楚。本研究旨在探讨 PD-L1 和 HER2 在消化道肿瘤中的表达情况。我们回顾性地确定了 HER2 阳性胃食管癌患者,并与 HER2 阴性患者进行匹配。我们对肿瘤标本进行了 HER2 状态和 PD-L1 表达的检测,包括以下评估:i)肿瘤细胞的染色程度(肿瘤比例评分,TPS),ii)肿瘤相关免疫细胞(TAIs)的染色,iii)界面模式和 iv)联合阳性评分(CPS)。HER2 阳性和阴性组各包含 59 名患者。在局部疾病患者中,TAIs 和界面模式的 PD-L1 表达与良好的预后相关(p=0.02,HR=0.8;p=0.04,HR=0.39),而晚期肿瘤患者的 TPS 与不良预后相关(p=0.02,HR=1.4)。这些影响与 HER2 无关。HER2 阳性和阴性患者的 PD-L1 表达在不同评估中具有相似的表现。未来的研究将表明 HER2 和 PD-L1 的双重抑制是否能改善这一特定患者群体的生存。