Chan Anthony W H, Tong Joanna H M, Chan Stephen L, Lai Paul B S, To Ka-Fai
Department of Anatomical and Cellular Pathology, State Key Laboratory in Oncology in South China, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Histopathology. 2014 Jun;64(7):935-50. doi: 10.1111/his.12342. Epub 2014 Feb 7.
The expression of stemness markers in hepatocellular carcinoma (HCC) is suggested to be associated with poor clinical outcome after surgical resection. There are few data on their independent prognostic role in addition to the existing AJCC TNM staging system.
The immunohistochemical expression of CD133, EpCAM, CK19 and CD56 was studied in a cohort of 282 surgical specimens collected from patients undergoing resection of primary HCC. CD133-positive HCCs were usually smaller in size (P = 0.002) and arose more frequently in cirrhotic liver (P = 0.002). CD133 expression was an independent prognostic factor for overall survival (hazard ratio 2.30, P < 0.001), and a highly potent prognostic factor in patients with stage I disease (hazard ratio 3.91, P = 0.001). EpCAM expression was associated with younger age (P < 0.001), smaller tumour size (P = 0.018) and poorer histological differentiation (P = 0.042). EpCAM immunoreactivity was an independent factor for disease-free survival in HCCs at all stages (hazard ratio 2.05, P = 0.001), stage II (hazard ratio 3.66, P = 0.010) and stages III/IV (hazard ratio 3.22, P = 0.001). Neither CK19 nor CD56 offered any independent prognostic value.
The prognostic role of CD133 was most significant in TNM stage I disease, while the prognostic role of EpCAM was more apparent in more advanced TNM stages.
肝细胞癌(HCC)中干性标志物的表达被认为与手术切除后的不良临床结局相关。除了现有的美国癌症联合委员会(AJCC)TNM分期系统外,关于它们独立的预后作用的数据很少。
对282例接受原发性肝癌切除术患者的手术标本进行队列研究,检测CD133、上皮细胞黏附分子(EpCAM)、细胞角蛋白19(CK19)和CD56的免疫组化表达。CD133阳性的肝癌通常体积较小(P = 0.002),且更常见于肝硬化肝脏(P = 0.002)。CD133表达是总生存的独立预后因素(风险比2.30,P < 0.001),并且在I期疾病患者中是一个高效的预后因素(风险比3.91,P = 0.001)。EpCAM表达与较年轻的年龄(P < 0.001)、较小的肿瘤大小(P = 0.018)和较差的组织学分化相关(P = 0.042)。EpCAM免疫反应性是所有阶段HCC无病生存的独立因素(风险比2.05,P = 0.001)、II期(风险比3.66,P = 0.010)和III/IV期(风险比3.22,P = 0.001)。CK19和CD56均未提供任何独立的预后价值。
CD133的预后作用在TNM I期疾病中最为显著,而EpCAM的预后作用在更晚期的TNM阶段更为明显。