Wang Hui-Ching, Chan Leong-Perng, Wu Chun-Chieh, Hsiao Hui-Hua, Liu Yi-Chang, Cho Shih-Feng, Du Jeng-Shiun, Liu Ta-Chih, Yang Cheng-Hong, Pan Mei-Ren, Moi Sin-Hua
Graduate Institute of Clinical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Department of Internal Medicine, Division of Hematology and Oncology, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
J Pers Med. 2021 Sep 13;11(9):908. doi: 10.3390/jpm11090908.
This study aimed to investigate whether the progression risk score (PRS) developed from cytoplasmic immunohistochemistry (IHC) biomarkers is available and applicable for assessing risk and prognosis in oral cancer patients. Participants in this retrospective case-control study were diagnosed between 2012 and 2014 and subsequently underwent surgical intervention. The specimens from surgery were stained by IHC for 16 cytoplasmic target markers. We evaluated the results of IHC staining, clinical and pathological features, progression-free survival (PFS), and overall survival (OS) of 102 oral cancer patients using a novel estimation approach with unsupervised hierarchical clustering analysis. Patients were stratified into high-risk (52) and low-risk (50) groups, according to their PRS; a metric consisting of cytoplasmic PLK1, PhosphoMet, SGK2, and SHC1 expression. Moreover, PRS could be extended for use in the Cox proportional hazard regression model to estimate survival outcomes with associated clinical parameters. Our study findings revealed that the high-risk patients had a significantly increased risk in cancer progression compared with low-risk patients (hazard ratio (HR) = 2.20, 95% confidence interval (CI) = 1.10-2.42, = 0.026). After considering the influences of demographics, risk behaviors, and tumor characteristics, risk estimation with PRS provided distinct PFS groups for patients with oral cancer ( = 0.017, = 0.019, and = 0.020). Our findings support that PRS could serve as an ideal biomarker for clinical use in risk stratification and progression assessment in oral cancer.
本研究旨在调查从细胞质免疫组织化学(IHC)生物标志物得出的进展风险评分(PRS)是否可用于评估口腔癌患者的风险和预后。这项回顾性病例对照研究的参与者在2012年至2014年期间被诊断出患有疾病,随后接受了手术干预。手术标本通过免疫组织化学法对16种细胞质靶标标志物进行染色。我们使用无监督层次聚类分析的新型估计方法评估了102例口腔癌患者的免疫组织化学染色结果、临床和病理特征、无进展生存期(PFS)和总生存期(OS)。根据患者的PRS,将其分为高风险组(52例)和低风险组(50例);PRS是一种由细胞质PLK1、磷酸化Met、SGK2和SHC1表达组成的指标。此外,PRS可扩展用于Cox比例风险回归模型,以估计生存结果及相关临床参数。我们的研究结果显示,与低风险患者相比,高风险患者癌症进展风险显著增加(风险比(HR)=2.20,95%置信区间(CI)=1.10 - 2.42,P = 0.026)。在考虑人口统计学、风险行为和肿瘤特征的影响后,PRS风险估计为口腔癌患者提供了不同的无进展生存期组(P = 0.017,P = 0.019,P = 0.020)。我们的研究结果支持PRS可作为口腔癌风险分层和进展评估临床应用的理想生物标志物。