Yoon Young Joon, Han Kwang-Hyub, Kim Do Young
Department of Internal Medicine, Yonsei University College of Medicine, 250 Seongsanno, Seodaemun-gu, Seoul, Korea.
Scand J Gastroenterol. 2009;44(7):861-6. doi: 10.1080/00365520902903034.
The role of serum prothrombin induced by vitamin K absence or antagonist-II (PIVKA-II) in the early detection of hepatocellular carcinoma (HCC) in patients with chronic hepatitis B virus (HBV) infection has not yet been clearly identified. The purpose of the study was to evaluate the sensitivity and specificity of PIVKA-II, alone or in combination with alpha-fetoprotein (AFP), for the detection of HCC during surveillance, and to determine whether PIVKA-II was a significant risk factor for patient survival.
During surveillance, 106 HCC cases and 100 non-HCC cases of chronic HBV infection were included. Sensitivity and specificity of AFP and PIVKA-II were obtained through cut-off values of 20 ng/ml and 40 mAU/ml, respectively. The Cox proportional hazards model was used to determine whether PIVKA-II would be a significant risk factor for patient survival.
The sensitivity rates of AFP and PIVKA-II were 57.5% (61/106) and 51.9% (55/106), respectively. Of 45 patients negative for AFP, 22 were positive for PIVKA-II. A combination of AFP and PIVKA-II increased the sensitivity to 78.3% (83/106). The specificities of AFP and PIVKA-II were 88.0% and 97.0%, respectively. PIVKA-II was not a significant risk factor for patient survival after multivariate analysis.
PIVKA-II can be used as a tumor marker for the early detection of HCC in patients with chronic HBV infection, especially in combination with AFP.
维生素K缺乏或拮抗剂-II诱导的血清凝血酶原(PIVKA-II)在慢性乙型肝炎病毒(HBV)感染患者肝细胞癌(HCC)早期检测中的作用尚未明确。本研究的目的是评估PIVKA-II单独或与甲胎蛋白(AFP)联合用于监测期间HCC检测的敏感性和特异性,并确定PIVKA-II是否为患者生存的显著危险因素。
在监测期间,纳入106例HCC病例和100例慢性HBV感染的非HCC病例。AFP和PIVKA-II的敏感性和特异性分别通过20 ng/ml和40 mAU/ml的临界值获得。采用Cox比例风险模型确定PIVKA-II是否为患者生存的显著危险因素。
AFP和PIVKA-II的敏感率分别为57.5%(61/106)和51.9%(55/106)。在45例AFP阴性的患者中,22例PIVKA-II阳性。AFP和PIVKA-II联合使用可将敏感性提高到78.3%(83/106)。AFP和PIVKA-II的特异性分别为88.0%和97.0%。多因素分析后,PIVKA-II不是患者生存的显著危险因素。
PIVKA-II可作为慢性HBV感染患者HCC早期检测的肿瘤标志物,尤其是与AFP联合使用时。