CEUS LI-RADS 联合甲胎蛋白在低危和高危患者肝细胞癌早期诊断中的价值。

Yafei Wu, Yuanyuan Chen, Lili Wei, Zhanling Ding, Shengfa Zhao, Shengxian Bao, Jiali Tang, Hang Li, Junjie Liu, Shangyong Zhu
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引用次数: 0

摘要

背景:我们发现,肝细胞癌(HCC)在非肝硬化患者中的发生率显著增加,而 HCC 经常被忽视或误诊。众所周知,对比增强超声(CEUS)肝脏成像报告和数据系统(LI-RADS)对高危 HCC 患者具有较高的诊断质量。因此,我们旨在比较 CEUS LI-RADS 对低危和高危人群的 HCC 检测准确性,以确认其在 HCC 风险增加但尚未被纳入 LI-RADS 高危人群的低危患者中的价值。此外,由于 CEUS LR-4 和 LR-M 类别中 HCC 的比例相对较高,而血清甲胎蛋白(AFP)是 HCC 最常用的生物标记物,且在临床上有效,因此我们尝试将 CEUS LR-4 和 LR-M 类别与甲胎蛋白相结合,进一步提高 CEUS LI-RADS 对低危和高危患者 HCC 的早期诊断能力:我们定义了高危组(HR)--包括在LI-RADS的高危患者中,低危组(LR)--不包括在LI-RADS的高危患者中,并在一项回顾性研究中纳入了189例LR和HR设置的HCC患者。所有病变均经组织病理学证实。比较了 CEUS LI-RADS 检测这两种患者 HCC 的准确性。此外,我们还提出了研究中的诊断算法(针对AFP>20 ng/ml的CEUS LR-4和LR-M患者)。我们分析了CEUS LI-RADS作为一种有效的方法,通过将LR-4和LR-M类别与AFP相结合,对LR和HR患者的HCC进行早期诊断的能力:结果:通过对比分析,CEUS LR-5类别对HR组HCC的特异性为78.4%,而对LR组的特异性为94.2%。同时,灵敏度(63.2% 对 63.0%)和阳性预测值(PPV)(75.0% 对 88.7%)在 LR 组和 HR 组之间没有差异(P = 0.990,P = 0.299)。值得注意的是,在我们的病例中,CEUS LR-4 和 LR-M 类别中的 HCC 比例较高,当我们将 CEUS LR-4 和 LR-M 类别与 AFP 结合时,LR 组的灵敏度显著提高了 21.0%(84.2%),HR 组提高了 16.0%(79.0%),HR 组的灵敏度在结合后有统计学差异(P = 0.014):结论:CEUS LR-5 分类在 LR 和 HR 患者的 HCC 诊断中具有实际意义。当 CEUS LR-4 和 LR-M 类别与 AFP 升高相结合时,CEUS LI-RADS 类别对 HCC 患者的早期检测能力进一步提高。
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The Value of CEUS LI-RADS combined with AFP in early diagnosis of hepatocellular carcinoma in low- and high-risk patients.

Background: We found that the occurrence of hepatocellular carcinoma (HCC) has increased significantly in non-cirrhotic individuals, with HCC being frequently overlooked or misdiagnosed. Contrast-enhanced ultrasound (CEUS) Liver Imaging Reporting and Data System (LI-RADS) is known to have a high diagnostic quality in high-risk HCC patients. Therefore, we aimed to compare the detection accuracy of CEUS LI-RADS for HCC between low- and high-risk individuals, to confirm its value in low-risk patients at increased risk of HCC, but not yet included in the high-risk groups of LI-RADS. In addition, since CEUS LR-4 and LR-M categories contain a relatively high proportion of HCC, and serum alpha-fetoprotein (AFP) is the most commonly used biomarker for HCC, and the clinically valid, we attempted to further improve the early diagnostic capability of CEUS LI-RADS for HCC in the low-risk and high-risk patients by combining CEUS LR-4 and LR-M categories with AFP.

Methods: We defined high-risk groups (HR)-included in the high-risk patients of LI-RADS, low-risk groups (LR)-not included in the high-risk patients of LI-RADS and enrolled 189 HCC patients with LR and HR settings in a retrospective study. All lesions were confirmed histopathologically. The CEUS LI-RADS accuracy for detecting HCC in these two patients was compared. In addition, the diagnostic algorithm in our study was proposed (for CEUS LR-4 and LR-M patients with AFP>20 ng/ml). we analyzed the ability of CEUS LI-RADS as a valid method of establishing the early diagnosis of HCC in LR and HR patients by combining LR-4 and LR-M categories with AFP.

Results: Through comparative analysis, the specificity of the CEUS LR-5 category for HCC in the HR group was 78.4%, whereas in the LR group, it was 94.2%. Meanwhile, the sensitivity (63.2% vs. 63.0%) and positive predictive value (PPV) (75.0% vs. 88.7%) did not differ between the LR and HR groups ( P = 0.990, P = 0.299). It is noteworthy that there were the high proportion of HCC in CEUS LR-4 and LR-M categories in our cases and when we combined CEUS LR-4 and LR-M categories with AFP significantly improved the sensitivity by 21.0% (84.2%) in the LR group, and by 16.0% (79.0%) in the HR group, with statistically difference in sensitivity after combination in the HR group ( P = 0.014).

Conclusions: The CEUS LR-5 category has real meaningful utility in the diagnosis of HCC in both LR and HR patients. The early detection power of the CEUS LI-RADS category for HCC patients was further increased when the CEUS LR-4 and LR-M categories were combined with elevated AFP.

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