Biasiolo Alessandra, Trotta Elisa, Fasolato Silvano, Ruvoletto Mariagrazia, Martini Andrea, Gallotta Andrea, Fassina Giorgio, Angeli Paolo, Gatta Angelo, Pontisso Patrizia
Department of Medicine, University of Padua, Italy.
Xeptagen SpA, Marghera (VE), Italy.
Dig Liver Dis. 2016 Feb;48(2):197-202. doi: 10.1016/j.dld.2015.10.022. Epub 2015 Oct 31.
Squamous cell carcinoma antigen (SCCA)-IgM complex has been described as a promising tool to identify patients with progressive liver disease at higher risk of hepatocellular carcinoma (HCC) development in retrospective studies.
To assess the clinical value of this biomarker in patients with cirrhosis in a prospective study.
Patients with overt cirrhosis were prospectively evaluated at 6-month intervals for HCC development and decompensation with clinical examination, liver ultrasound, α-fetoprotein measurement. SCCA-IgM was measured in serum by immunoenzymatic assay. Median follow-up duration was 52 months (range 12-68 months).
70 patients (26% male; mean age 56±10 years) were enrolled. The main aetiological factors were alcohol (44%) and hepatitis C (34%). Baseline values of SCCA-IgM were significantly higher in patients who developed HCC. Positivity of the biomarker at baseline was associated with a significantly shorter HCC-free survival, while α-fetoprotein (cut off >20 ng/ml) was not significant. SCCA-IgM positivity and hepatitis C were significant prognostic factors for HCC development. The biomarker was not associated with the development of clinical complications of cirrhosis.
This prospective study demonstrates that in patients with cirrhosis SCCA-IgM is associated with HCC development and may be useful for clinical management of cirrhotic patients at higher risk of HCC development.
在回顾性研究中,鳞状细胞癌抗原(SCCA)-IgM复合物已被描述为一种有前景的工具,用于识别进展性肝病患者发生肝细胞癌(HCC)风险较高的患者。
在前瞻性研究中评估这种生物标志物在肝硬化患者中的临床价值。
对显性肝硬化患者每隔6个月进行前瞻性评估,以观察HCC的发生和失代偿情况,评估方法包括临床检查、肝脏超声、甲胎蛋白测量。通过免疫酶测定法检测血清中的SCCA-IgM。中位随访时间为52个月(范围12 - 68个月)。
共纳入70例患者(男性占26%;平均年龄56±10岁)。主要病因是酒精(44%)和丙型肝炎(34%)。发生HCC的患者SCCA-IgM的基线值显著更高。基线时该生物标志物呈阳性与无HCC生存期显著缩短相关,而甲胎蛋白(临界值>20 ng/ml)则无显著相关性。SCCA-IgM阳性和丙型肝炎是HCC发生的显著预后因素。该生物标志物与肝硬化临床并发症的发生无关。
这项前瞻性研究表明,在肝硬化患者中,SCCA-IgM与HCC发生相关,可能有助于对发生HCC风险较高的肝硬化患者进行临床管理。