Delu Gan, Yali Wang, Xin Yang, Juan Huang, Lijun Zhang, Bianqin Guo, Pu Li, Dan Gou
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引用次数: 0
摘要
目的:肝细胞癌(HCC)的诊断和预后在临床实践中提出了重大挑战。本研究旨在评估肿瘤异常蛋白(TAP)、维生素K缺失致凝血酶原- ii (PIVKA-II)和甲胎蛋白(AFP)在HCC诊断中的临床应用,并探讨其在HCC经动脉化疗栓塞患者中的预后意义。方法:共纳入93例HCC患者,101名健康人作为对照。采集新鲜静脉血,化学发光免疫法检测TAP、PIVKA-II、AFP水平。结果:HCC患者与健康人在TAP、PIVKA-II和AFP水平上存在显著差异。TAP、AFP和PIVKA-II联合检测对HCC的诊断效果较好。经动脉化疗栓塞并达到完全缓解(CR)的患者化疗前血清TAP、AFP和PIVKA-II水平较低。在CR与部分缓解(PR)、CR与稳定(SD)、CR与进展性疾病(PD)之间,TAP、AFP、PIVKA-II水平存在显著差异。结论:TAP、PIVKA-II、AFP联合检测对HCC有较好的诊断价值。化疗前血清TAP、AFP和PIVKA-II水平升高与不良的临床化疗反应显著相关。
Diagnostic value of TAP, PIVKA-II, and AFP in hepatocellular carcinoma and their prognostic value for patients treated with transarterial chemoembolization.
Objective: The diagnosis and prognosis of hepatocellular carcinoma (HCC) present significant challenges in clinical practice. This study aimed to evaluate the clinical utility of tumor abnormal protein (TAP), Prothrombin induced by vitamin K absence-II (PIVKA-II), and alpha-fetoprotein (AFP) in diagnosing HCC as well as to investigate their prognostic significance in patients with HCC undergoing transarterial chemoembolization.
Methods: A total of 93 HCC patients were enrolled and 101 healthy individuals served as controls. Fresh venous blood samples were collected, and TAP, PIVKA-II, and AFP levels were measured by chemiluminescence immunoassay.
Results: Significant differences in TAP, PIVKA-II, and AFP levels were found between HCC patients and healthy individuals. The combined assay of TAP, AFP, and PIVKA-II showed better diagnostic performance for HCC. Patients who underwent transarterial chemoembolization and achieved complete response (CR) had lower levels of prechemotherapy serum TAP, AFP, and PIVKA-II. There are significant differences in levels of TAP, AFP, and PIVKA-II between CR and partial response (PR), CR and stable disease (SD), and CR and progressive disease (PD).
Conclusion: Combined detection of TAP, PIVKA-II, and AFP has better diagnostic performance for HCC. Higher levels of prechemotherapy serum TAP, AFP, and PIVKA-II are significantly associated with poor clinical chemoresponse.