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Brunsing et al. Hepatoma Res 2020;6:59  I  http://dx.doi.org/10.20517/2394-5079.2020.50                                      Page 13 of 16

               KEY POINTS
               There are three variations of AMRI for HCC surveillance (non-contrast, dynamic, and hepatobiliary), each
               offering unique advantages.


               There is a growing body of literature suggesting the sensitivity of AMRI may be higher than US, however
               existing data does not yet support widespread adoption of AMRI-based HCC surveillance by international
               guidelines.


               Current utilization of AMRI should focus on patients in whom US-based HCC surveillance is compromised.

               Clinical trials directly comparing AMRI to US for HCC surveillance in high-risk populations are underway.

               Continued evolution of MRI technology is expected to increase the robustness of AMRI for HCC detection.


               RECOMMENDATION
               We cautiously recommend AMRI in situations where US is compromised. With regard to the exact
               approach - NC-AMRI, Dynamic-AMRI, or HBP-AMRI - all are reasonable. There is not yet sufficient
               evidence to recommend one approach over another. Hence, we leave protocol selection to the individual
               radiologist, referrer, and institution, considering patient preferences.


               DECLARATIONS
               Authors’ contributions
               Made substantial contributions to structure and content of the text and figures: Brunsing RL, Fowler KJ,
               Yokoo T, Cunha GM, Sirlin CB, Marks RM
               Made substantial contributions to synthesizing edits from all authors: Brunsing RL

               Availability of the data and materials
               Not applicable.

               Financial support and sponsorship
               Dr. Sirlin's research is supported in part by NIH (1R01CA249765-01). The content is solely the responsibility of
               the authors and does not necessarily represent the official views of the National Institutes of Health.

               Conflicts of interest
               Brunsing RL reports a grant from GE. Fowler KJ reports grant support from GE and Bayer; personal
               consultation fees from 12 Sigma, Innovis, and Bayer. Yokoo T reports no conflict of interest. Cunha GM
               reports no conflict of interest. Sirlin CB reports grants from GE, Siemens, Philips, Bayer, Foundation of
               NIH, Gilead; personal consultation fees from Blade, Boehringer, and Epigenomics; consultation under
               the auspices of the University to AMRA, BMS, Exact Sciences, GE Digital, and IBM-Watson; lab service
               agreements from Enanta, Gilead, ICON, Intercept, Nusirt, Shire, Synageva, Takeda; royalties from Wolters
               Kluwer for educational material outside the submitted work. Marks RM reports no conflicts of interest. The
               views expressed in this article are those of the authors and do not necessarily reflect the official policy or
               position of the Department of the Navy, Department of Defense, or the U.S. Government.

               Ethical approval and consent to participate
               Not applicable.


               Consent for publication
               Not applicable.
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