Department of Radiology, Clinical Hospital Centre Rijeka, Rijeka, Croatia.
Department of Transfusion Medicine and Haematology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy.
Cochrane Database Syst Rev. 2022 May 6;5(5):CD014798. doi: 10.1002/14651858.CD014798.pub2.
Hepatocellular carcinoma occurs mostly in people with chronic liver disease and ranks sixth in terms of global incidence of cancer, and third in terms of cancer deaths. In clinical practice, magnetic resonance imaging (MRI) is used as a second-line diagnostic imaging modality to confirm the presence of focal liver lesions suspected as hepatocellular carcinoma on prior diagnostic test such as abdominal ultrasound or alpha-fetoprotein, or both, either in surveillance programmes or in clinical settings. According to current guidelines, a single contrast-enhanced imaging study (computed tomography (CT) or MRI) showing typical hallmarks of hepatocellular carcinoma in people with cirrhosis is considered valid to diagnose hepatocellular carcinoma. The detection of hepatocellular carcinoma amenable to surgical resection could improve the prognosis. However, a significant number of hepatocellular carcinomas do not show typical hallmarks on imaging modalities, and hepatocellular carcinoma may, therefore, be missed. There is no clear evidence of the benefit of surveillance programmes in terms of overall survival: the conflicting results can be a consequence of inaccurate detection, ineffective treatment, or both. Assessing the diagnostic accuracy of MRI may clarify whether the absence of benefit could be related to underdiagnosis. Furthermore, an assessment of the accuracy of MRI in people with chronic liver disease who are not included in surveillance programmes is needed for either ruling out or diagnosing hepatocellular carcinoma.
Primary: to assess the diagnostic accuracy of MRI for the diagnosis of hepatocellular carcinoma of any size and at any stage in adults with chronic liver disease. Secondary: to assess the diagnostic accuracy of MRI for the diagnosis of resectable hepatocellular carcinoma in adults with chronic liver disease, and to identify potential sources of heterogeneity in the results.
We searched the Cochrane Hepato-Biliary Group Controlled Trials Register, the Cochrane Hepato-Biliary Group Diagnostic Test of Accuracy Studies Register, the Cochrane Library, MEDLINE, Embase, and three other databases to 9 November 2021. We manually searched articles retrieved, contacted experts, handsearched abstract books from meetings held during the last 10 years, and searched for literature in OpenGrey (9 November 2021). Further information was requested by e-mails, but no additional information was provided. No data was obtained through correspondence with investigators. We applied no language or document-type restrictions.
Studies assessing the diagnostic accuracy of MRI for the diagnosis of hepatocellular carcinoma in adults with chronic liver disease, with cross-sectional designs, using one of the acceptable reference standards, such as pathology of the explanted liver and histology of resected or biopsied focal liver lesion with at least a six-month follow-up.
At least two review authors independently screened studies, extracted data, and assessed the risk of bias and applicability concerns, using the QUADAS-2 checklist. We presented the results of sensitivity and specificity, using paired forest plots, and we tabulated the results. We used a hierarchical meta-analysis model where appropriate. We presented uncertainty of the accuracy estimates using 95% confidence intervals (CIs). We double-checked all data extractions and analyses.
We included 34 studies, with 4841 participants. We judged all studies to be at high risk of bias in at least one domain because most studies used different reference standards, often inappropriate to exclude the presence of the target condition, and the time interval between the index test and the reference standard was rarely defined. Regarding applicability, we judged 15% (5/34) of studies to be at low concern and 85% (29/34) of studies to be at high concern mostly owing to characteristics of the participants, most of whom were on waiting lists for orthotopic liver transplantation, and due to pathology of the explanted liver being the only reference standard. MRI for hepatocellular carcinoma of any size and stage: sensitivity 84.4% (95% CI 80.1% to 87.9%) and specificity 93.8% (95% CI 90.1% to 96.1%) (34 studies, 4841 participants; low-certainty evidence). MRI for resectable hepatocellular carcinoma: sensitivity 84.3% (95% CI 77.6% to 89.3%) and specificity 92.9% (95% CI 88.3% to 95.9%) (16 studies, 2150 participants; low-certainty evidence). The observed heterogeneity in the results remains mostly unexplained. The sensitivity analyses, which included only studies with clearly prespecified positivity criteria and only studies in which the reference standard results were interpreted without knowledge of the results of the index test, showed no variation in the results.
AUTHORS' CONCLUSIONS: We found that using MRI as a second-line imaging modality to diagnose hepatocellular carcinoma of any size and stage, 16% of people with hepatocellular carcinoma would be missed, and 6% of people without hepatocellular carcinoma would be unnecessarily treated. For resectable hepatocellular carcinoma, we found that 16% of people with resectable hepatocellular carcinoma would improperly not be resected, while 7% of people without hepatocellular carcinoma would undergo inappropriate surgery. The uncertainty resulting from the high risk of bias in the included studies and concerns regarding their applicability limit our ability to confidently draw conclusions based on our results.
肝细胞癌主要发生在患有慢性肝脏疾病的人群中,其全球癌症发病率排名第六,癌症死亡率排名第三。在临床实践中,磁共振成像(MRI)被用作二线诊断成像方式,以确认先前诊断性检查(如腹部超声或甲胎蛋白,或两者都有)中疑似为肝细胞癌的局灶性肝脏病变的存在,无论是在监测计划中还是在临床环境中。根据现行指南,在肝硬化患者中,单次对比增强成像研究(计算机断层扫描(CT)或 MRI)显示出典型的肝细胞癌特征,即可被认为有效诊断肝细胞癌。检测到适合手术切除的肝细胞癌可以改善预后。然而,大量的肝细胞癌在影像学上没有显示出典型的特征,因此可能会漏诊。目前没有明确的证据表明监测计划在总体生存方面有获益:相互矛盾的结果可能是由于检测不准确、治疗无效或两者兼而有之。评估 MRI 的诊断准确性可以明确是否因诊断不足而导致获益减少。此外,还需要评估 MRI 在未纳入监测计划的慢性肝脏疾病患者中的准确性,以排除或诊断肝细胞癌。
主要目的:评估 MRI 对慢性肝脏疾病成人中任何大小和任何阶段肝细胞癌的诊断准确性。次要目的:评估 MRI 对慢性肝脏疾病成人中可切除肝细胞癌的诊断准确性,并确定结果中潜在的异质性来源。
我们检索了 Cochrane 肝胆疾病组对照试验注册库、Cochrane 肝胆疾病组诊断准确性研究注册库、Cochrane 图书馆、MEDLINE、Embase 和另外三个数据库,检索日期截至 2021 年 11 月 9 日。我们手动检索了检索到的文章,联系了专家,手检了过去 10 年会议的摘要集,并在 OpenGrey(2021 年 11 月 9 日)中搜索了文献。通过电子邮件请求了更多信息,但没有提供更多信息。没有通过与研究者通信获取数据。我们没有对语言或文件类型施加任何限制。
研究评估 MRI 对慢性肝脏疾病成人中肝细胞癌的诊断准确性,采用横断面设计,使用一种可接受的参考标准,如肝切除术的病理和经皮活检或切除的局灶性肝脏病变的组织学,且具有至少 6 个月的随访。
至少两名综述作者独立筛选研究、提取数据,并使用 QUADAS-2 清单评估偏倚风险和适用性问题。我们使用配对森林图展示了敏感性和特异性的结果,并列出了结果。在适当的情况下,我们使用了分层荟萃分析模型。我们使用 95%置信区间(CI)表示准确性估计的不确定性。我们对所有数据提取和分析进行了双重核对。
我们纳入了 34 项研究,共 4841 名参与者。我们判断所有研究在至少一个领域都存在高偏倚风险,因为大多数研究使用了不同的参考标准,这些标准往往不排除目标疾病的存在,并且指数试验和参考标准之间的时间间隔很少被定义。关于适用性,我们判断 15%(5/34)的研究为低关注,85%(29/34)的研究为高关注,主要原因是参与者的特征,其中大多数是等待肝移植的患者,以及肝切除术的病理是唯一的参考标准。MRI 对任何大小和阶段的肝细胞癌的诊断:敏感性 84.4%(95%CI 80.1%至 87.9%),特异性 93.8%(95%CI 90.1%至 96.1%)(34 项研究,4841 名参与者;低质量证据)。MRI 对可切除肝细胞癌的诊断:敏感性 84.3%(95%CI 77.6%至 89.3%),特异性 92.9%(95%CI 88.3%至 95.9%)(16 项研究,2150 名参与者;低质量证据)。结果中的观察到的异质性在很大程度上仍未得到解释。包括仅具有明确阳性标准的研究和仅对指数试验结果不知情的情况下解释参考标准结果的研究的敏感性分析显示,结果没有变化。
我们发现,使用 MRI 作为二线成像方式来诊断任何大小和阶段的肝细胞癌,将有 16%的肝细胞癌患者会被漏诊,6%的非肝细胞癌患者将接受不必要的治疗。对于可切除的肝细胞癌,我们发现将有 16%的可切除肝细胞癌患者不能得到适当的切除,而 7%的非肝细胞癌患者将接受不适当的手术。纳入研究的高偏倚风险以及对其适用性的关注限制了我们根据研究结果得出结论的能力。