The Diagnostic Value Of Serum Glypican-3 In The Diagnosis Of Hepatocellular Carcinoma: A Systematic Review And Meta-Analysis

Arinze I. Aninworie, MD, MSc
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Abstract

Background and aim: Hepatocellular carcinoma (HCC) is the second leading cause of cancer-related deaths worldwide. It is curable in the early stages but has a poor prognosis when advanced. Current diagnostic protocols for the early stages of HCC are inefficient. Serum Glypican-3 (GPC-3) is a promising serum tumour marker in diagnosing HCC, and its diagnostic value has been explored in various studies. The outcomes, however, continue to be inconsistent and controversial. This systematic review and meta-analysis aimed to investigate the diagnostic accuracy of serum GPC-3 in hepatocellular carcinoma. This study included recent papers not captured in previous meta-analyses. Method: PUBMED, MEDLINE, Cochrane Library, and CINAHL databases were systematically searched according to preferred reporting items for a systematic review and meta-analysis of diagnostic test accuracy studies guidelines. Studies on the diagnostic accuracy of serum GPC-3 in HCC were selected. The Quality assessment of diagnostic accuracy studies 2 (QUADAS-2) tools were used to assess the quality of selected studies. Sensitivity, specificity, and other diagnostic parameters were pooled using the random effect model. The Summary receiver operating characteristic (sROC) was used to summarise the diagnostic accuracy of Serum GPC-3. Results: Eleven studies were included in this systematic review. The pooled sensitivity, specificity, and 95% confidence intervals (CIs) were 0.60 (0.57-0.62) and 0.67(0.64-0.70), respectively. The pooled positive and negative likelihood ratios and 95% CIs were 2.11 (1.51-2.93) and 0.59 (0.51-0.68), respectively; the pooled diagnostic odds ratio and the 95% CI were 4.07 (2.37-6.98), the area under the sROC curve was 0.7194. Conclusion: This meta-analysis has shown that Serum GPC-3 has an acceptable diagnostic value in diagnosing HCC compared to benign chronic liver diseases. A higher-quality study with a larger sample size is necessary to thoroughly assess the diagnostic utility of serum GPC-3.
血清Glypican-3在肝细胞癌诊断中的诊断价值:系统回顾和荟萃分析
背景和目的:肝细胞癌(HCC)是全球癌症相关死亡的第二大原因。它在早期是可以治愈的,但在晚期预后很差。目前HCC早期诊断方案效率低下。血清Glypican-3 (GPC-3)是一种很有希望诊断HCC的血清肿瘤标志物,其诊断价值已在各种研究中得到探讨。然而,结果仍然是不一致和有争议的。本系统综述和荟萃分析旨在探讨血清GPC-3在肝细胞癌诊断中的准确性。这项研究包括了在以前的荟萃分析中没有收录的最新论文。方法:系统检索PUBMED、MEDLINE、Cochrane Library和CINAHL数据库,根据首选报告项目对诊断测试准确性研究指南进行系统评价和荟萃分析。选择血清GPC-3对HCC诊断准确性的研究。使用诊断准确性研究质量评估2 (QUADAS-2)工具评估所选研究的质量。使用随机效应模型对敏感性、特异性和其他诊断参数进行汇总。采用综合受试者工作特征(sROC)评价血清GPC-3的诊断准确性。结果:本系统综述纳入了11项研究。合并敏感性、特异性和95%置信区间(ci)分别为0.60(0.57-0.62)和0.67(0.64-0.70)。合并阳性、阴性似然比和95% ci分别为2.11(1.51 ~ 2.93)和0.59 (0.51 ~ 0.68);合并诊断优势比和95% CI为4.07 (2.37 ~ 6.98),sROC曲线下面积为0.7194。结论:本荟萃分析显示,与良性慢性肝病相比,血清GPC-3在诊断HCC方面具有可接受的诊断价值。为了彻底评估血清GPC-3的诊断效用,有必要进行更高质量、更大样本量的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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