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LI-RADS 版本 2018 钆塞酸增强 MRI 上的靶样外观:鉴别 HCC 和非 HCC 恶性肿瘤的观察者间协议和诊断性能。

LI-RADS Version 2018 Targetoid Appearances on Gadoxetic Acid-Enhanced MRI: Interobserver Agreement and Diagnostic Performance for the Differentiation of HCC and Non-HCC Malignancy.

机构信息

Department of Radiology and Center for Imaging Science, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro Gangnam-gu, Seoul 06351, Republic of Korea.

Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul, Republic of Korea.

出版信息

AJR Am J Roentgenol. 2022 Sep;219(3):421-432. doi: 10.2214/AJR.22.27380. Epub 2022 Mar 23.

Abstract

In LI-RADS version 2018, observations showing at least one of five targetoid appearances in different sequences or postcontrast phases are categorized LR-M, indicating likely non-hepatocellular carcinoma (HCC) malignancy. The purpose of this study was to evaluate interobserver agreement for LI-RADS targetoid appearances among a large number of radiologists of varying experience and the diagnostic performance of targetoid appearances for differentiating HCC from non-HCC malignancy. This retrospective study included 100 patients (76 men, 24 women; mean age, 58 ± 9 [SD] years) at high risk of HCC who underwent gadoxetic acid-enhanced MRI within 30 days before hepatic tumor resection (25 randomly included patients with non-HCC malignancy [13, intrahepatic cholangiocarcinoma; 12, combined HCC-cholangiocarcinoma]; 75 matched patients with HCC). Eight radiologists (four more experienced [8-15 years]; four less experienced [1-5 years]) from seven institutions independently assessed observations for the five targetoid appearances and LI-RADS categorization. Interobserver agreement and diagnostic performance for non-HCC malignancy were evaluated. Interobserver agreement was poor for peripheral washout (κ = 0.20); moderate for targetoid transitional phase or hepatobiliary phase appearance (κ = 0.33), delayed central enhancement (κ = 0.37), and targetoid restriction (κ = 0.43); and substantial for rim arterial phase hyperenhancement (κ = 0.61). Agreement was fair for at least one targetoid appearance (κ = 0.36) and moderate for at least two, three, or four targetoid appearances (κ = 0.43-0.51). Agreement for individual targetoid appearances was not significantly different between more experienced and less experienced readers other than for targetoid restriction (κ = 0.63 vs 0.43; = .001). Agreement for at least one targetoid appearance was fair among more experienced (κ = 0.29) and less experienced (κ = 0.37) reviewers. Agreement for at least two, three, or four targetoid appearances was moderate to substantial among more experienced reviewers (κ = 0.45-0.63) and moderate among less experienced reviewers (κ = 0.42-0.56). Existing LR-M criteria of at least one targetoid appearance had median accuracy for non-HCC malignancy of 62%, sensitivity of 84%, and specificity of 54%. For all reviewers, accuracy was highest when at least three (median accuracy, 79%; sensitivity, 68%; specificity, 82%) or four (median accuracy, 80%; sensitivity, 54%; specificity, 88%) targetoid appearances were required. Targetoid appearances and LR-M categorization exhibited considerable interobserver variation among both more and less experienced reviewers. Requiring multiple targetoid appearances for LR-M categorization improved interobserver agreement and diagnostic accuracy for non-HCC malignancy.

摘要

在 LI-RADS 版本 2018 中,如果在不同序列或对比后相中观察到至少有五种靶样外观中的一种,则将其归类为 LR-M,表示可能是非肝细胞癌 (HCC) 恶性肿瘤。本研究的目的是评估不同经验水平的大量放射科医生对 LI-RADS 靶样外观的观察者间一致性,以及靶样外观在区分 HCC 与非 HCC 恶性肿瘤方面的诊断性能。这项回顾性研究纳入了 100 名(76 名男性,24 名女性;平均年龄 58 ± 9[SD]岁) HCC 高危患者,他们在肝肿瘤切除前 30 天内接受了钆塞酸增强 MRI(25 名随机纳入的非 HCC 恶性肿瘤患者[13 名肝内胆管癌;12 名 HCC-胆管癌];75 名匹配的 HCC 患者)。来自七个机构的八位放射科医生(四位经验更丰富[8-15 年];四位经验较少[1-5 年])独立评估了五种靶样外观和 LI-RADS 分类的观察结果。评估了观察者间一致性和对非 HCC 恶性肿瘤的诊断性能。对周围洗脱的观察者间一致性较差(κ=0.20);靶样过渡相或肝胆相期外观(κ=0.33)、延迟中央增强(κ=0.37)和靶样限制(κ=0.43)的观察者间一致性为中度;边缘动脉期高增强(κ=0.61)的观察者间一致性为显著。至少有一个靶样外观的观察者间一致性为适度(κ=0.36),至少有两个、三个或四个靶样外观的观察者间一致性为中度至高度(κ=0.43-0.51)。除靶样限制外(κ=0.63 对 0.43;=0.001),经验丰富的读者与经验较少的读者之间在单个靶样外观的观察者间一致性上无显著差异。经验丰富的读者(κ=0.29)和经验较少的读者(κ=0.37)的至少一个靶样外观的观察者间一致性为适度。经验丰富的读者中,至少有两个、三个或四个靶样外观的观察者间一致性为中度至高度(κ=0.45-0.63),经验较少的读者中为中度(κ=0.42-0.56)。现有的 LR-M 标准对非 HCC 恶性肿瘤的准确性中位数为 62%,敏感性为 84%,特异性为 54%。对于所有审查员,当至少有三个(中位数准确性为 79%;敏感性为 68%;特异性为 82%)或四个(中位数准确性为 80%;敏感性为 54%;特异性为 88%)靶样外观时,准确性最高。靶样外观和 LR-M 分类在经验丰富和经验较少的审查员中均表现出相当大的观察者间差异。对 LR-M 分类的多个靶样外观要求提高了非 HCC 恶性肿瘤的观察者间一致性和诊断准确性。

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