Overview
OPTN 2014
OPTN policy for liver transplant
candidates with HCC (in USA).
LI-RADS 2014
Comprehensive imaging diagnosis
system for HCC.
Target population
Intended users
All radiologists.
Categorization of
observations
HCC
Indeterminate
Benign
Untreated observations
LR-1: definitely benign
LR-2: probably benign
LR-3: intermediate probability
LR-4: probably HCC
LR-5: definitely HCC
LR-5V: tumor in vein
LR-M: probably malignant, not
specific for HCC
Treated observations
LR-Treated
Imaging methods
addressed
Imaging features
addressed
No
No
Yes
No
No
Yes
Reporting templates
No
Yes
Yes
LI-RADS
Intro
v2014
LR-Treated
My edits to the
diagonal boxes.
Untreated observation
Treated observation
Definitely
benign
Probably
benign
LR-1
LR-2
LR-M
Tumor in vein
LR-5V
Arterial phase
hypo- or isoenhancement
Arterial phase
hyperenhancement
Diameter (mm):
< 20
20
< 10
10-19
20
Washout
None:
LR-3
LR-3
LR-3
LR-3
LR-4
Capsule
One:
LR-3
LR-4
LR-4
LR-4
LR-5
LR-5
Two:
LR-4
LR-4
LR-4
LR-5
LR-5
Threshold growth
LR-4
LR-5
LI-RADS Category
LR-1
Definitely
Benign
LR-2
Probably
Benign
Intermediate
probability
for HCC
LR-3
Probably
HCC
Concept: High probability observation is HCC but there is not 100% certainty.
LR-4
LR-5
Definitely
HCC
LR-5V
LR-M
Probable
malignancy, not
specific for HCC
LR-Treated
Treated
Observation
Definition: Observation with imaging features suggestive but not diagnostic of a benign
entity.
Definition: Observation that does not meet criteria for other LI-RADS categories.
Definition: Observation with imaging features suggestive but not diagnostic of HCC.
LI-RADS Features
Major
Arterial phase features
Arterial phase hypo- or isoenhancement
Arterial phase hyperenhancement
Diameter
For arterial phase hypo- or
iso-enhancing masses:
Diameter < 20mm
Diameter 20 mm
For arterial phase hyperenhancing masses:
Diameter < 10mm
Diameter 10-19mm
Diameter 20 mm
Washout appearance
Capsule appearance
Threshold growth
Mild-moderate T2 hyperintensity
Restricted diffusion
Corona enhancement*
Mosaic architecture*
Nodule-in-nodule architecture*
Intra-lesional fat*
Lesional iron sparing
Lesional fat sparing
Blood products
Diameter increase less than
threshold growth
Hepatobiliary phase hypointensity
Distinctive rim*
Homogeneous marked T2
hyper-intensity
Homogeneous marked T2 or
T2* hypo-intensity
Undistorted vessels traversing
observation
Parallels blood pool
enhancement
Diameter reduction
Diameter stability 2 years
Hepatobiliary-phase
isointensity
LI-RADS
v2014
LR-1
versus
LR-2
LR-2
LR-2
versus
LR-3
LR-3
LR-3
versus
LR-4
LR-3
LR-4
versus
LR-5
LR-4
LR-3
versus
LR-M
LR-3
LR-4
versus
LR-M
LR-M
LR-5
versus
LR-M
LR-M
Tie-breaking rules: Schematic diagram illustrates application of tie-breaking rules to adjust category. If, after application of ancillary
features, a radiologist is still unsure about the final category for an observation, tie-breaking rules should be applied. The tie-breaking rules
move observations to a category with a lower degree of certainty.
Introduction
What is LI-RADS (Liver Imaging Reporting And Data System)?
A system of standardized terminology and criteria to interpret and report imaging examinations of the liver.
Supported and endorsed by the American College of Radiology (ACR).
LI-RADS is a dynamic document: it will be expanded and refined as knowledge accrues and in response to
user feedback.
Who is developing LI-RADS?
LI-RADS is being developed by an ACR-supported committee of diagnostic radiologists with expertise in liver
imaging.
The committee receives input from hepatobiliary surgeons, hepatologists, hepatopathologists, and
interventionalists.
In what patient population does LI-RADS apply?
LI-RADS currently applies to patients with cirrhosis or at risk for HCC.
What imaging modalities are addressed by LI-RADS?
LI-RADS currently applies to CT and MRI performed with extracellular and hepatobiliary contrast agents.
Surveillance ultrasound findings as incorporated into AASLD guidelines for diagnosis of HCC
Who can use LI-RADS?
LI-RADS may be used by community and academic radiologists.
How does LI-RADS work?
LI-RADS categorizes observations from LR-1 to LR-5, reflecting probability of benignity or HCC in at-risk
patients.