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对比增强超声联合全氟丁烷在肝细胞癌诊断中的应用:成像相和诊断标准的比较。

Contrast-Enhanced Ultrasound With Perfluorobutane for Hepatocellular Carcinoma Diagnosis: Comparison of Imaging Phases and Diagnostic Criteria.

机构信息

Department of Radiology, Seoul National University Hospital, Seoul, Korea.

Department of Radiology, Seoul National University College of Medicine, 101 Daehangno, Jongno-gu, Seoul, 03080, Korea.

出版信息

AJR Am J Roentgenol. 2024 Feb;222(2):e2330156. doi: 10.2214/AJR.23.30156. Epub 2023 Nov 22.

DOI:10.2214/AJR.23.30156
PMID:37991335
Abstract

Contrast-enhanced ultrasound (CEUS) with perfluorobutane has used varying protocols and diagnostic criteria for hepatocellular carcinoma (HCC). The purpose of this article was to assess diagnostic performance for HCC of CEUS with perfluorobutane in high-risk patients using various criteria. This retrospective post hoc study evaluating individual patient data from three earlier prospective studies from one hospital included 204 patients (136 men, 68 women; mean age, 63 ± 11 [SD] years) at high risk of HCC with 213 liver observations. Patients underwent CEUS using perfluorobutane from March 2019 to June 2022. Three radiologists (the examination's operator and two subsequent reviewers) independently interpreted examinations, assessing arterial, portal venous (arterial phase completion through 2 minutes), transitional (2-5 minutes after injection), and Kupffer (≥ 10 minutes after injection) phase findings. Six criteria for HCC were tested: 1, any arterial phase hyperenhancement (APHE) with Kupffer phase hypoenhancement; 2, nonrim APHE with Kupffer phase hypoenhancement; 3, nonrim APHE with portal venous washout; 4, nonrim APHE with portal venous washout and/or Kupffer phase hypoenhancement; 5, nonrim APHE with portal venous and/or transitional washout; 6, nonrim APHE with any of portal venous washout, transitional washout, or Kupffer phase hypoenhancement. Depending on the criteria, observations were instead deemed to be a non-HCC malignancy if showing rim APHE, early washout (at < 1 minute), or marked washout (at 2 minutes). Reference was pathology for malignant observations and pathology or imaging follow-up for benign observations. Diagnostic performance was assessed, pooling readers' data. Criterion 1 (no recognized features of non-HCC malignancy) had highest sensitivity (86.9%) but lowest specificity (43.2%) for HCC. Compared with nonrim APHE and portal venous washout (criterion 3), the addition of Kupffer phase hypoenhancement (criterion 4), transitional washout (criterion 5), or either feature (criterion 6) significantly increased sensitivity (34.4% vs 62.6-64.2%) and accuracy (61.8% vs 75.1-76.5%), but significantly decreased specificity (98.5% vs 91.9-94.1%). Criteria 2, 4, 5, and 6 (all incorporating transitional washout and/or Kupffer phase hypoenhancement) showed no significant differences in sensitivity (62.6-64.2%), specificity (91.9-94.1%), or accuracy (75.1-76.5%). Recognition of features of non-HCC malignancy improved specificity for HCC. Incorporation of the findings of transitional washout and/or Kupffer phase hypoenhancement improved sensitivity and accuracy, albeit lowered specificity, versus arterial and portal venous findings alone, without further performance variation among criteria incorporating those two findings. Kupffer phase acquisition may be optional for observations classified as HCC or non-HCC malignancy by arterial, portal venous, and transitional phases.

摘要

对比增强超声(CEUS)使用全氟丁烷已用于肝细胞癌(HCC)的不同方案和诊断标准。本文旨在使用各种标准评估高危患者使用全氟丁烷的 CEUS 对 HCC 的诊断性能。本回顾性事后研究评估了来自一家医院的三个先前前瞻性研究的个体患者数据,包括 204 名(136 名男性,68 名女性;平均年龄 63 ± 11 [SD] 岁)高危 HCC 患者的 213 个肝脏观察结果。患者于 2019 年 3 月至 2022 年 6 月接受了使用全氟丁烷的 CEUS。三位放射科医生(检查操作员和两位后续审阅者)独立解读了动脉、门静脉(注射后 2 分钟内的动脉期完成)、过渡(注射后 2-5 分钟)和库普弗(注射后≥10 分钟)期发现。测试了 6 项 HCC 标准:1. 任何动脉期高增强(APHE)伴库普弗期低增强;2. 无边缘 APHE 伴库普弗期低增强;3. 无边缘 APHE 伴门静脉洗脱;4. 无边缘 APHE 伴门静脉洗脱和/或库普弗期低增强;5. 无边缘 APHE 伴门静脉和/或过渡洗脱;6. 无边缘 APHE 伴门静脉洗脱、过渡洗脱或库普弗期低增强中的任何一种。根据标准,如果观察结果显示边缘 APHE、早期洗脱(<1 分钟)或明显洗脱(2 分钟),则将其视为非 HCC 恶性肿瘤。恶性观察结果以病理学为参考,良性观察结果以病理学或影像学随访为参考。汇集了读者的数据来评估诊断性能。标准 1(无非 HCC 恶性肿瘤的公认特征)对 HCC 的敏感性(86.9%)最高,但特异性(43.2%)最低。与无边缘 APHE 和门静脉洗脱(标准 3)相比,添加库普弗期低增强(标准 4)、过渡洗脱(标准 5)或两者(标准 6)显著提高了敏感性(34.4%对 62.6-64.2%)和准确性(61.8%对 75.1-76.5%),但特异性显著降低(98.5%对 91.9-94.1%)。标准 2、4、5 和 6(均包含过渡洗脱和/或库普弗期低增强)在敏感性(62.6-64.2%)、特异性(91.9-94.1%)或准确性(75.1-76.5%)方面无显著差异。对非 HCC 恶性肿瘤特征的认识提高了 HCC 的特异性。与仅基于动脉和门静脉发现相比,结合过渡洗脱和/或库普弗期低增强可提高敏感性和准确性,尽管特异性降低,而不同标准之间的性能变化无差异,这些标准均包含这些发现。对于通过动脉、门静脉和过渡期分类为 HCC 或非 HCC 恶性肿瘤的观察结果,库普弗期采集可能是可选的。

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