| Literature DB >> 35480538 |
Liping Lu1, Xuming Pan2.
Abstract
Non-contrast MRI is used for identifying patients with hepatocellular carcinoma (HCC), especially among high-risk patients with cirrhosis or chronic viral hepatitis. The accuracy of non-contrast MRI has been investigated with varying results. We performed this meta-analysis to consolidate the evidence on the accuracy of non-contrast MRI for the detection of HCC. We conducted a systematic search in the databases of PubMed Central, SCOPUS, MEDLINE, EMBASE and Cochrane from inception till November 2020. We used the STATA software "Midas" package for meta-analysis. We included 15 studies with 3,756 patients. The pooled sensitivity and specificity of non-contrast MRI for HCC detection were 84% (95%CI, 78%-88%) and 94% (95%CI, 91%-97%). The positive likelihood ratio was 14.9 (95% CI, 9.0-24.7) and the negative one 0.17 (0.12-0.23). The overall quality of the studies was high. We found significant heterogeneity based on chi-square test results and I2 statistic > 75%. Deek's test showed the absence of publication bias. We found that non-contrast MRI has high sensitivity and specificity as a tool for detecting HCC. Studies exploring its accuracy in different ethnic populations are required to strengthen the evidence. Copyright: © Pakistan Journal of Medical Sciences.Entities:
Keywords: Hepatocellular Carcinoma; Magnetic Resonance Imaging; Meta-analysis; Validation studies
Year: 2022 PMID: 35480538 PMCID: PMC9002405 DOI: 10.12669/pjms.38.3.5142
Source DB: PubMed Journal: Pak J Med Sci ISSN: 1681-715X Impact factor: 1.088
Fig.1Search strategy.
Characteristics of the included studies (n=15)
| Author, year, Country | Study design | Study participants | MRI Procedure and Intent | Reference standard | Mean age (in years) |
|---|---|---|---|---|---|
| Chan et al 2019 | Retrospective | 564 patients at high risk of HCC (cirrhosis, HBV/ hepatitis C virus/other risk factors) for HCC diagnosis | Non-contrast MRI study created by selecting axial T2- weighted sequence with 160-ms echo time, all four axial T1-weighted Dixon sequences | cMRI | 63 |
| Chung et al 2011 | Retrospective | 46 patients who underwent hepatic MRI for HCC surveillance | DWI on a single-shot spin-echo Echo Planar Imaging sequence that combined the two diffusion gradients before & after 180° pulse | Histopathology | 59.6 |
| Han et al 2018 | Retrospective | 247 patients with initial diagnosed HCC & no previous treatment history, within Milan criteria for HCC diagnosis | Liver MRIs on a 3T system with an 8-channel phased array torso coil. Respiratory triggered fast spin echo T2WI with fat suppression & dual gradient echo T1WI using in-phase and opposed-phase | Histopathology/ cMRI/FU | 59.6 |
| Hardie et al 2011 | Retrospective | 37 patients who had undergone liver transplantation for HCC diagnosis | DWI on a single-shot echo-planar imaging with repetition time/echo time 4800/94; matrix 192¥100; parallel imaging factor 2; gradients with b-value 50, 500, 1000 s/mm2 | Histopathology | 56.6 |
| Jalli et al 2015 | Prospective | 96 cirrhosis patients referred to gastroenterology follow-up for HCC diagnosis | Respiratory triggered single-shot fat-suppressed echo-planar DWI sequence in axial plane with acquisition correction on TR/TE, 2100/85 ms; 6mm slice thickness; with b value 50, 400, 800 s/mm2 | Histopathology | NA |
| Kim et al 2014 | Retrospective | 182 patients with chronic hepatitis or liver cirrhosis for HCC diagnosis | DW-MRI single-shot echo planar imaging and simultaneous respiratory triggering on TR/TE 1600/70. b-value of 0, 100, 800 s/mm2; SENSE acceleration factor, 4.0; field-of-view, 35×35 cm; | Histopathology | 57 |
| Kim et al 2020 | Retrospective | 226 patients with a history of cirrhosis or chronic liver disease who underwent MRI of the liver for HCC surveillance | Liver MRI scans on a 3T system with a16-channel phased-array torso coil. Respiratory-triggered fast-spin echo T2WI with fat suppression and dual-gradient echo T1WI. DWI with echo planar imaging using b values of 0, 50, 400, 800 s/mm2 | Histopathology | 60.1 |
| Min et al 2018 | Retrospective | 483 patients who underwent surveillance after hepatectomy | MR images on a 3.0 T whole-body MR system with a 16-channel phased-array coil as the receiver coil. | Histopathology | 58 |
| Park et al 2012 | Retrospective | 52 patients who underwent liver transplantation for HCC surveillance | Liver MRI on different state-of-the-art 1.5-T systems and torso phased-array coils. Parallel imaging and field of view of 300-400 mm | Histopathology | 56 |
| Park et al 2020 | Retrospective | 1057 patients > 20 years diagnosed histologically/ radiologically as having cirrhosis with HCC surveillance | MRI on a 1.5-T scanner. Breath-hold dual gradient-echo T1-weighted images, DWI with a respiratory triggered turbo spin echo, single-shot echo planar sequence images with b-values of 0, 50, 500 s/mm2 | Histopathology and radiologic hallmark | 56.4 |
| Shankar et al 2016 | Prospective | 20 patients presenting to hepatology clinic with chronic liver disease for HCC diagnosis | Abdominal MR on 3T imaging system using a body coil. The protocol included T1, T2 weighted axial imaging including both non-fat and fat-suppressed sequence, axial DWI | Cytological grading | NA |
| Sutherland et al 2016 | Prospective | 192 patients > 18 years referred by gastroenterology with chronic liver disease for HCC surveillance | MRI scan sequence comprised respiratory-gated DWI with TR 2500; TE 80; slice thickness 8 mm; distance factor 30%, FOV read 400 mm, and b values of 100, 400, 800 | Histopathology | 58 |
| Violi et al 2020 | Retrospective | 237 patients (≥ 18 years) with cirrhosis, chronic hepatitis B for HCC surveillance | Non-contrast MRI, including axial non-fat-suppressed T2WI single-shot echo-planar imaging + axial fat suppressed DWI single-shot echo-planar imaging | Histopathology | 58 |
| Whang et al 2020 | Retrospective | 263 patients with liver cirrhosis or other risk factors without prior history of HCC treatment | All MR images were acquired using 3.0-T MR system. Respiratory-triggered fast spin echo T2WI with fat suppression, 3D dual gradient echo T1WI using in- and opposed-phase. DWI with echo planar imaging using b values of 0, 50, 500, 800 s/mm2 | Histopathology | 64 |
| Xu et al 2010 | Retrospective | 54 patients who had undergone routine c-MRI & DWI before surgery for HCC diagnosis | All MR examinations were performed on a 1.5-T superconducting scanner with combination of a 6-channel phased-array body coil & spine array coil | Histopathology | 66.2 |
Fig.2Forest plot showing pooled sensitivity and specificity for non-contrast MRI.
Fig.3Likelihood scatter gram.
Fig.4Fagan nomogram