期刊文献+

血清异常凝血酶原和甲胎蛋白联合检测对原发性肝癌的临床价值 被引量:51

The clinical value of serum PIVKA- II and AFP detection for hepatocellular carcinoma
原文传递
导出
摘要 目的探讨血清异常凝血酶原(PIVKA-Ⅱ)和甲胎蛋白(AFP)在原发性肝癌(HCC)诊断和疗效监测中的价值。方法病例对照研究。用化学发光法和电化学发光法检测2013年8月至2014年3月期间青岛大学附属医院148例肝细胞癌、37例肝内胆管细胞癌、44例胃、结直肠癌、63例肝硬化、38例慢性乙型肝炎、57例体检健康者血清PIVKA—Ⅱ和AFP水平,分别分析两者单独及联合检测诊断HCC的受试者工作曲线下面积(ROC—AUC)、敏感度和特异性;分析血清PIVKA—Ⅱ和AFP水平与肿瘤直径大小及TNM分期的相关性;比较HCC患者治疗前后两指标血清水平的变化。结果肝细胞癌组血清PIVKA一1I和AFP水平均高于肝内胆管细胞癌组、胃结直肠癌组、肝硬化组、慢性乙型肝炎组和健康对照组(PIVKA—Ⅱ:U值分别为866.50、424.00、958.00、292.00和448.00;AFP:U值分别为713.00、440.50、1182.00、614.00和399.00,P均〈0.001)。两指标单独检测和联合检测对HCC组患者的ROC—AUC均差异无统计学意义(P〉0.05)。PIVKA-Ⅱ诊断HCC的敏感度(87.16%)高于AFP(68.92%,=4.73,P〈0.05),PIVKA—Ⅱ和AFP联合检测诊断HCC的敏感度(93.24%)高于PIVKA—Ⅱ单项检测(87.16%,校正x^2=64.70,P〈0.01),但特异度之间比较差异均无统计学意义(P〉0.05)。Spearman秩相关分析显示,血清PIVKA-Ⅱ和AFP水平与肿瘤大小均呈正相关(相关系数分别为0.716和0.475,P均〈0.001)。随肿瘤直径增大,HCC患者PIVKA—Ⅱ和AFP水平逐渐升高(日值分别为72.70、37.02,P均〈0.001);阳性率也逐渐提高(x^2值分别为26.74、21.62,P均〈0.001)。按国际肿瘤TNM分期,Ⅰ~Ⅳ期血清PIVKA-Ⅱ和AFP水平(H值分别为46.63、21.38,P均〈0.001)与阳性率(PIVKA—Ⅱ:X2=20.40,P〈0.01;AFP:X2=8.33,P〈0.05)也随TNM肿瘤� Objective To discuss the clinical value of Protein induced by Vitamin K Antagonist-Ⅱ (PIVKA-lI ) and alpha-Fetoproteins (AFP) in diagnosing hepatocellular carcinoma (HCC) and monitoring the treatment effects. Methods Patients were recruited by the Affiliated Hospital of Qingdao University, from August 2013 to March 2014. Serum levels of PIVKA-Ⅱ and AFP were measured by both chemiluminescence assay (CLIA) and electrochemiluminescencc assay (ECLA) in patients with HCC (n = 148 ), intrahepatic cholangioceUular carcinoma ( n = 37 ), gastric cancer and colorectal cancer ( n = 44), cirrhosis ( n = 63 ), chronic hepatitis B (n = 38) and healthy subjects (n = 57). To analyze the areas under the receiver operating characteristic curves (ROC-AUC) and to compare the sensitivity and specificity ofsingle PIVKA- U or AFP assay, and the combined detection. To analyze the correlation of PIVKA- Ⅱand both tumor size and TNM staging, so do AFP, respectively. To compare the serum level changes of the two indicators in HCC patients before and after treatment. Results The serum levels of both PIYKA-Ⅱ and AFP in HCC group were higher than that in intrahepatic cholangiocellular carcinoma, gastric cancer and colorectal cancer, cirrhosis, chronic hepatitis B and healthy subjects groups ( PIVKA- Ⅱ : U = 866. 50, 424. 00, 958.00, 292.00 and 448.00 ; AFP:U=713.00, 440.50, 1 182.00, 614.00 and 399.00, P〈0. 001) . The ROC-AUCs of the single PIVKA- II or AFP assay and the combined detection in HCC group were not statistically different ( P 〉 0. 05 ) . The sensitivity of PIVKA- Ⅱ ( 87. 16% ) was higher than that of AFP (68.92% ,X2 =4. 73 ,P 〈 0. 05)in diagnosing HCC; the sensitivity of the combined detection of PIVKA-I1 and AFP (93.24%) was higher than that of PIVKA- Ⅱ itself ( 87.16%, adjusted X2 = 64. 70, P 〈 0. 01 ) ; while the specificities among them did not show statistical significance (P 〉 0. 05). Tested by Spearman rank correlation, t
出处 《中华检验医学杂志》 CAS CSCD 北大核心 2014年第12期928-932,共5页 Chinese Journal of Laboratory Medicine
关键词 肝细胞 蛋白质前体 凝血酶原 生物学标记 甲胎蛋白类 Carcinoma, hepatocellular Protein precursors Prothrombin Biologicalmarkers Alpha-Fetoproteins
  • 相关文献

参考文献1

二级参考文献33

  • 1[1]Bosch FX,Ribes J,Diaz M,Cleries R.Primary liver cancer:worldwide incidence and trends.Gastroenterology 2004; 127:S5-16 被引量:1
  • 2[2]Bosch FX,Ribes J,Borras J.Epidemiology of primary liver cancer.Semin Liver Dis 1999; 19:271-285 被引量:1
  • 3[3]Zaman SN,Melia WM,Johnson RD,Portmann BC,Johnson PJ,Williams R.Risk factors in development of hepatocellular carcinoma in cirrhosis:prospective study of 613 patients.Lancet 1985; 1:1357-1360 被引量:1
  • 4[4]Benvegnu L,Gios M,Boccato S,Alberti A.Natural history of compensated viral cirrhosis:a prospective study on the incidence and hierarchy of major complications.Gut 2004; 53:744-749 被引量:1
  • 5[5]Liaw YF,Tai DI,Chu CM,Lin DY,Sheen IS,Chen TJ,Pao CC.Early detection of hepatocellular carcinoma in patients with chronic type B hepatitis.A prospective study.Gastroenterology 1986; 90:263-267 被引量:1
  • 6[6]Zhang BH,Yang BH,Tang ZY.Randomized controlled trial of screening for hepatocellular carcinoma.J Cancer Res Clin Oncol 2004; 130:417-421 被引量:1
  • 7[7]E1-Serag HB,Mason AC,Key C.Trends in survival of patients with hepatocellular carcinoma between 1977 and 1996in the United States.Hepatology 2001; 33:62-65 被引量:1
  • 8[8]Bruix J,Sherman M,Llovet JM,Beaugrand M,Lencioni R,Burroughs AK,Christensen E,Pagliaro L,Colombo M,Rodes J.EASL panel of rxperts on HCC.Clinical management of hepatocellular carcinoma.Conclusions of the barcelona-2000EASL conference.European sssociation for the dtudy of the liver.J Hepatol 2001; 35:421-430 被引量:1
  • 9[9]Liebman HA,Furie BC,Tong MJ,Blanchard RA,Lo KJ,Lee SD,Coleman MS,Furie B.Des-gamma-carboxy (abnormal)prothrombin as a serum marker of primary hepatocellular carcinoma.N Engl J Med 1984; 310:1427-1431 被引量:1
  • 10[10]Soulier JP,Gozin D,Lefrere JJ.A new method to assay desgamma-carboxyprothrombin.Results obtained in 75 cases of hepatocellular carcinoma.Gastroenterology 1986; 91:1258-1262 被引量:1

共引文献18

同被引文献282

引证文献51

二级引证文献360

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部