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Review
. 2024 Nov;313(2):e232408.
doi: 10.1148/radiol.232408.

CT/MRI LI-RADS 2024 Update: Treatment Response Assessment

Affiliations
Review

CT/MRI LI-RADS 2024 Update: Treatment Response Assessment

Anum Aslam et al. Radiology. 2024 Nov.

Erratum in

  • Erratum for: CT/MRI LI-RADS 2024 Update: Treatment Response Assessment.
    Aslam A, Chernyak V, Tang A, Miller FH, Bashir M, Do R, Sirlin C, Lewandowski RJ, Kim CY, Kielar AZ, Kambadakone AR, Yarmohammadi H, Kim E, Owen D, Charalel RA, Shenoy-Bhangle A, Burke LM, Mendiratta-Lala M. Aslam A, et al. Radiology. 2025 Feb;314(2):e259002. doi: 10.1148/radiol.259002. Radiology. 2025. PMID: 39998379 Free PMC article. No abstract available.

Abstract

With the rising incidence of hepatocellular carcinoma, there has been increasing use of local-regional therapy (LRT) to downstage or bridge to transplant, for definitive treatment, and for palliation. The CT/MRI Liver Imaging Reporting and Data System (LI-RADS) Treatment Response Assessment (TRA) algorithm provides guidance for step-by-step tumor assessment after LRT and standardized reporting. Current evidence suggests that the algorithm performs well in the assessment of tumor response to arterial embolic and loco-ablative therapies and fair when assessing response to radiation-based therapies, with limited data to validate the latter. Both evidence-based and expert-based refinements of the algorithm are needed to improve its diagnostic accuracy after varying types of LRT. This review provides an overview of the challenges and limitations of the LI-RADS TRA algorithm version 2017 and discusses the refinements introduced in the updated 2024 LI-RADS algorithm for CT/MRI.

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Conflict of interest statement

Disclosures of conflicts of interest: A.A. No relevant relationships. V.C. Consulting fees from Bayer and Gilead. F.H.M. Consulting fees from Bayer; medical advisory board member for Guerbet. M.B. Grants from Siemens Healthineers, Madrigal Pharmaceuticals, Carmot Therapeutics, Corcept Therapeutics, and NGM Bio; editorial board member for the Journal of Magnetic Resonance Imaging. R.D. Grant to institution from the National Institutes of Health/National Cancer Institute; royalties from Elsevier; consulting fees from Ascelia Pharma. C.S. Grants to institution from the American College of Radiology, Bayer, GE HealthCare, Pfizer, Gilead, Philips, and Siemens; laboratory service agreements with OrsoBio, Enanta, Gilead, ICON, Intercept, NuSirt, Shire, Synageva, and Takeda; royalties from Medscape and Wolters Kluwer; consulting fees from Altimmune, Ascelia Pharma, Blade, Boehringer, Epigenomics, and Guerbet; consulting fees to institution from AMRA, BMS, Exact Sciences, IBM-Watson, and Pfizer; payment for educational symposia; travel support from Fundación Santa Fe, CADI, Stanford, Jornada Paulista de Radiologia, and Ascelia Pharma; participation on a data safety monitoring board or advisory board for Quantix Bio (unpaid); former chief medical officer for Livivos and former member of the Society of Abdominal Radiology board of directors; stock and stock options in Livivos; equipment loan to institution from GE HealthCare; member of the LI-RADS Steering Committee and LI-RADS working groups (unpaid). R.J.L. Grant to institution from the National Institutes of Health; consulting fees from Boston Scientific, BD, Varian, and AstraZeneca; payment for lectures from Boston Scientific; president elect of the Society of Interventional Radiology (SIR). C.Y.K. Consulting fees from Boston Scientific, ACI/Humacyte, and Baylis Medical. A.Z.K. Travel support from the Canadian Association of Radiologists; president of the Canadian Association of Radiologists. A.R.K. Grants from GE HealthCare, Pancreatic Cancer Action Network, Philips, and Bayer; royalties from Elsevier; consulting fees from Bayer; travel support from International Diagnostic Course Davos. H.Y. Research grants from Guerbet and Thompson Family Foundation; advisory board member for AstraZeneca and Guerbet; patent planned, issued, or pending with the Yarmohammadi Foundation. E.K. Advisory board member for AstraZeneca, Roche/Genentech, Boston Scientific, Eisai, and Varian Interventional Solutions. D.O. Research funding from AstraZeneca and Varian; honorarium from UpToDate. R.A.C. Grants from GERRAF (via the Association of Academic Radiology [AUR], funded by GE HealthCare), SIR Foundation, Instylla, and Food and Drug Administration; consulting fees from TriSalus Life Sciences and Embolx; payment for lectures from the Cleveland Clinic, Sirtex Medical, American College of Surgery, and TriSalus Life Sciences; support for travel from Digestive Disease Interventions, SIR, TriSalus Life Sciences, and AUR; participation on a data safety monitoring board or advisory board for Embolx; chair of the SIR Quality Data Analytics Committee; stock or stock options in Embolx. A.S.B. No relevant relationships. L.M.B. No relevant relationships. M.M.L. No relevant relationships.

Figures

None
Graphical abstract
CT/MRI Liver Imaging Reporting and Data System (LI-RADS) Treatment
Response Assessment (TRA) algorithm, version 2024 (v2024), for (A) nonradiation
treatment and (B) radiation-based treatment. LRT = local-regional therapy, LR-TR
= LI-RADS treatment response. * = Examples include complete lesion
disappearance, no lesional enhancement, smooth perilesional enhancement, or
parenchymal perfusional changes without masslike enhancement.
Figure 1:
CT/MRI Liver Imaging Reporting and Data System (LI-RADS) Treatment Response Assessment (TRA) algorithm, version 2024 (v2024), for (A) nonradiation treatment and (B) radiation-based treatment. LRT = local-regional therapy, LR-TR = LI-RADS treatment response. * = Examples include complete lesion disappearance, no lesional enhancement, smooth perilesional enhancement, or parenchymal perfusional changes without masslike enhancement.
Liver Imaging Reporting and Data System (LI-RADS) treatment response
(LR-TR) Nonviable after microwave ablation (MWA). MRI scans in a 62-year-old
male patient with cirrhosis who presented with a 2.4-cm LI-RADS 5
observation in segment V show (A) arterial phase hyperenhancement (arrow)
and (B) portal venous phase washout with capsule (arrow). (C) Patient
underwent microwave ablation, and MRI scan 3 months later shows a 3.2-cm
treatment cavity demonstrating intrinsic T1 precontrast hyperintense signal
secondary to coagulation necrosis (red arrow). Note the treatment cavity is
8–10 mm larger than the tumor itself to ensure adequate treatment of
microscopic disease surrounding the tumor. (D) Arterial phase MRI scan shows
no intralesional masslike enhancement and smooth perilesional enhancement,
categorized as LR-TR Nonviable (arrow). Note the surrounding perfusional
changes.
Figure 2:
Liver Imaging Reporting and Data System (LI-RADS) treatment response (LR-TR) Nonviable after microwave ablation (MWA). MRI scans in a 62-year-old male patient with cirrhosis who presented with a 2.4-cm LI-RADS 5 observation in segment V show (A) arterial phase hyperenhancement (arrow) and (B) portal venous phase washout with capsule (arrow). (C) Patient underwent microwave ablation, and MRI scan 3 months later shows a 3.2-cm treatment cavity demonstrating intrinsic T1 precontrast hyperintense signal secondary to coagulation necrosis (red arrow). Note the treatment cavity is 8–10 mm larger than the tumor itself to ensure adequate treatment of microscopic disease surrounding the tumor. (D) Arterial phase MRI scan shows no intralesional masslike enhancement and smooth perilesional enhancement, categorized as LR-TR Nonviable (arrow). Note the surrounding perfusional changes.
Liver Imaging Reporting and Data System (LI-RADS) treatment response
(LR-TR) Viable after transarterial chemoembolization. MRI scans in a
75-year-old male patient with hepatitis C–related cirrhosis show (A)
a 3.3-cm observation in segment II of the liver that demonstrates arterial
phase hyperenhancement (arrow), plus washout and capsule (not shown),
categorized as LI-RADS 5. (B) Arterial phase MRI scan 1 month after
transarterial chemoembolization shows no residual intralesional enhancement
(arrow), and (C) there is smooth perilesional enhancement without masslike
areas of enhancement (arrow), yielding LR-TR Nonviable. One year following
transarterial chemoembolization, (D) noncontrast MRI scan shows a new 4.5
× 1.0-cm area of irregular T1 hypointense signal (arrows) with (E)
masslike enhancement (arrows) and (F) washout and capsule (arrows) along the
margin of the previous transarterial chemoembolization–treated
hepatocellular carcinoma, yielding LR-TR Viable.
Figure 3:
Liver Imaging Reporting and Data System (LI-RADS) treatment response (LR-TR) Viable after transarterial chemoembolization. MRI scans in a 75-year-old male patient with hepatitis C–related cirrhosis show (A) a 3.3-cm observation in segment II of the liver that demonstrates arterial phase hyperenhancement (arrow), plus washout and capsule (not shown), categorized as LI-RADS 5. (B) Arterial phase MRI scan 1 month after transarterial chemoembolization shows no residual intralesional enhancement (arrow), and (C) there is smooth perilesional enhancement without masslike areas of enhancement (arrow), yielding LR-TR Nonviable. One year following transarterial chemoembolization, (D) noncontrast MRI scan shows a new 4.5 × 1.0-cm area of irregular T1 hypointense signal (arrows) with (E) masslike enhancement (arrows) and (F) washout and capsule (arrows) along the margin of the previous transarterial chemoembolization–treated hepatocellular carcinoma, yielding LR-TR Viable.
Liver Imaging Reporting and Data System (LI-RADS) treatment response
(LR-TR) Equivocal after microwave ablation. MRI scans in a 76-year-old
female patient with alcohol-related cirrhosis show a 1.7-cm segment VI
observation demonstrating (A) arterial phase hyperenhancement (arrow), (B)
washout and capsule (arrow), (C) mild T2 hyperintense signal (arrow), and
(D) restricted diffusion (arrow), categorized as LI-RADS 5. (E) MRI scan 3
months after microwave ablation shows irregular perilesional rim enhancement
on arterial phase (arrow), while the (F) corresponding portal venous phase
image shows no finding (arrow). (G) T2-weighted image shows subtle
corresponding mild hyperintense signal (arrow) with (H) restricted diffusion
(arrow). In Treatment Response Assessment version 2017, this would be LR-TR
Equivocal; however, in version 2023, this can be upgraded to LR-TR Viable
based on the presence of ancillary features. (I) Precontrast T1-weighted MRI
scan 6 months after microwave ablation shows central coagulation necrosis
(arrow), with (J) increasing nodular masslike enhancement along the margin
(arrow), which demonstrates (K) corresponding mild T2 hyperintense signal
(arrow) and (L) restricted diffusion (arrow), yielding LR-TR Viable. The
patient was re-treated with microwave ablation.
Figure 4:
Liver Imaging Reporting and Data System (LI-RADS) treatment response (LR-TR) Equivocal after microwave ablation. MRI scans in a 76-year-old female patient with alcohol-related cirrhosis show a 1.7-cm segment VI observation demonstrating (A) arterial phase hyperenhancement (arrow), (B) washout and capsule (arrow), (C) mild T2 hyperintense signal (arrow), and (D) restricted diffusion (arrow), categorized as LI-RADS 5. (E) MRI scan 3 months after microwave ablation shows irregular perilesional rim enhancement on arterial phase (arrow), while the (F) corresponding portal venous phase image shows no finding (arrow). (G) T2-weighted image shows subtle corresponding mild hyperintense signal (arrow) with (H) restricted diffusion (arrow). In Treatment Response Assessment version 2017, this would be LR-TR Equivocal; however, in version 2023, this can be upgraded to LR-TR Viable based on the presence of ancillary features. (I) Precontrast T1-weighted MRI scan 6 months after microwave ablation shows central coagulation necrosis (arrow), with (J) increasing nodular masslike enhancement along the margin (arrow), which demonstrates (K) corresponding mild T2 hyperintense signal (arrow) and (L) restricted diffusion (arrow), yielding LR-TR Viable. The patient was re-treated with microwave ablation.
Liver Imaging Reporting and Data System (LI-RADS) treatment response
(LR-TR) Nonviable after transarterial radioembolization. Arterial phase MRI
scans in a 48-year-old female patient show a LI-RADS 5 observation (circle)
in segment VII/VI of the liver ([A] arterial phase hyperenhancement and [B]
washout and capsule). Arterial phase MRI scans (C) 3 months, (D) 9 months,
and (E) 15 months after transarterial radioembolization show no masslike
intralesional enhancement and smooth perilesional rim enhancement (arrow),
yielding LR-TR Nonviable at all time points. Note the surrounding
wedge-shaped parenchymal perfusional changes corresponding to the vascular
distribution, compatible with radiation fibrosis and the slowly developing
parenchymal atrophy from fibrosis.
Figure 5:
Liver Imaging Reporting and Data System (LI-RADS) treatment response (LR-TR) Nonviable after transarterial radioembolization. Arterial phase MRI scans in a 48-year-old female patient show a LI-RADS 5 observation (circle) in segment VII/VI of the liver ([A] arterial phase hyperenhancement and [B] washout and capsule). Arterial phase MRI scans (C) 3 months, (D) 9 months, and (E) 15 months after transarterial radioembolization show no masslike intralesional enhancement and smooth perilesional rim enhancement (arrow), yielding LR-TR Nonviable at all time points. Note the surrounding wedge-shaped parenchymal perfusional changes corresponding to the vascular distribution, compatible with radiation fibrosis and the slowly developing parenchymal atrophy from fibrosis.
Liver Imaging Reporting and Data System (LI-RADS) treatment response
(LR-TR) Viable after transarterial radioembolization. MRI scans in a 58-year
old male patient with (A) biopsy-proven LR-M (peripheral rim enhancement at
arterial phase with progressive enhancement at portal venous and delayed
phase) hepatocellular carcinoma in segment VIII (arrow). Arterial phase
images (B) 3 months and (C) 9 months after transarterial radioembolization
show no intralesional enhancement and smooth perilesional rim enhancement
without masslike enhancement (arrow), yielding LR-TR Nonviable. (D) MRI
scans 15 months after transarterial radioembolization show a new nodular
area of arterial phase hyperenhancement along the 7 o’clock aspect of
the treatment cavity (arrow), which demonstrates (E) washout (arrow) on the
portal venous phase image, yielding LR-TR Viable.
Figure 6:
Liver Imaging Reporting and Data System (LI-RADS) treatment response (LR-TR) Viable after transarterial radioembolization. MRI scans in a 58-year old male patient with (A) biopsy-proven LR-M (peripheral rim enhancement at arterial phase with progressive enhancement at portal venous and delayed phase) hepatocellular carcinoma in segment VIII (arrow). Arterial phase images (B) 3 months and (C) 9 months after transarterial radioembolization show no intralesional enhancement and smooth perilesional rim enhancement without masslike enhancement (arrow), yielding LR-TR Nonviable. (D) MRI scans 15 months after transarterial radioembolization show a new nodular area of arterial phase hyperenhancement along the 7 o’clock aspect of the treatment cavity (arrow), which demonstrates (E) washout (arrow) on the portal venous phase image, yielding LR-TR Viable.
Liver Imaging Reporting and Data System treatment response (LR-TR)
Viable after stereotactic body radiation therapy (SBRT). Pretreatment MRI
scans in an 89-year-old female patient with hepatitis C–related
cirrhosis presenting with 3.6-cm biopsy-proven hepatocellular carcinoma show
(A) arterial phase peripheral rim enhancement and heterogeneous central
enhancement (arrow), with (B) restricted diffusion (arrow) and (C) mild
hyperintense T2-weighted signal (arrow), yielding category LR-M.
(D–F) MRI scans acquired 3 months after stereotactic body radiation
therapy show the treated lesion measuring 2.0 cm, with (D) persistent
irregular masslike enhancement in the lesion with surrounding parenchymal
perfusional changes related to postradiation changes (arrow), (E) mild
restricted diffusion (arrow), and (F) mild persistent T2-weighted
hyperintense signal (arrow), yielding LR-TR Nonprogressing. On MRI scans (G)
6 and (J) 12 months after stereotactic body radiation therapy, the treated
observation measures 1.4 cm and 1.5 cm, respectively, with no intralesional
enhancement but increasing parenchymal fibrosis (arrow), (H, K) loss of
restricted diffusion (arrow), and (I, L) decreasing T2-weighted
hyperintensity (arrow), yielding LR-TR Nonviable at both time points.
(M–O) Fifteen-month follow-up MRI scans show interval increase in
size of the treatment cavity, measuring 2.7 cm with (M) new intralesional
enhancement (arrow), (N) areas of increased restricted diffusion (arrow),
and (O) T2-weighted hyperintense signal corresponding to the areas of new
internal enhancement (arrow), yielding LR-TR Viable.
Figure 7:
Liver Imaging Reporting and Data System treatment response (LR-TR) Viable after stereotactic body radiation therapy (SBRT). Pretreatment MRI scans in an 89-year-old female patient with hepatitis C–related cirrhosis presenting with 3.6-cm biopsy-proven hepatocellular carcinoma show (A) arterial phase peripheral rim enhancement and heterogeneous central enhancement (arrow), with (B) restricted diffusion (arrow) and (C) mild hyperintense T2-weighted signal (arrow), yielding category LR-M. (D–F) MRI scans acquired 3 months after stereotactic body radiation therapy show the treated lesion measuring 2.0 cm, with (D) persistent irregular masslike enhancement in the lesion with surrounding parenchymal perfusional changes related to postradiation changes (arrow), (E) mild restricted diffusion (arrow), and (F) mild persistent T2-weighted hyperintense signal (arrow), yielding LR-TR Nonprogressing. On MRI scans (G) 6 and (J) 12 months after stereotactic body radiation therapy, the treated observation measures 1.4 cm and 1.5 cm, respectively, with no intralesional enhancement but increasing parenchymal fibrosis (arrow), (H, K) loss of restricted diffusion (arrow), and (I, L) decreasing T2-weighted hyperintensity (arrow), yielding LR-TR Nonviable at both time points. (M–O) Fifteen-month follow-up MRI scans show interval increase in size of the treatment cavity, measuring 2.7 cm with (M) new intralesional enhancement (arrow), (N) areas of increased restricted diffusion (arrow), and (O) T2-weighted hyperintense signal corresponding to the areas of new internal enhancement (arrow), yielding LR-TR Viable.
Liver Imaging Reporting and Data System (LI-RADS) treatment response
(LR-TR) Nonprogressing. Images in a 54-year-old male patient with hepatitis
C and alcohol-related cirrhosis presenting with an α-fetoprotein
level of 143 ng/mL and a 3.8-cm segment IV observation with (A) arterial
phase hyperenhancement (arrow) and washout and capsule (not shown),
categorized as LI-RADS 5. (B) MRI arterial phase scan 1 month after
transarterial radioembolization, with an α-fetoprotein level of 12.5
ng/mL, shows minimal residual intralesional enhancement (11 o’clock
position) and smooth perilesional rim enhancement (arrow), yielding LR-TR
Nonprogressing. (C) On the MRI arterial phase scan 5 months after
transarterial radioembolization, the treatment cavity was smaller, with
decreasing intralesional enhancement and smooth perilesional rim enhancement
(arrow), yielding LR-TR Nonprogressing. (D) On the MRI arterial phase scan
18 months after transarterial radioembolization, there was no residual
intralesional enhancement, and the treatment cavity had decreased in size
(arrow), yielding LR-TR Nonviable. Note the overlying capsular retraction
from radiation fibrosis, an expected finding after transarterial
radioembolization.
Figure 8:
Liver Imaging Reporting and Data System (LI-RADS) treatment response (LR-TR) Nonprogressing. Images in a 54-year-old male patient with hepatitis C and alcohol-related cirrhosis presenting with an α-fetoprotein level of 143 ng/mL and a 3.8-cm segment IV observation with (A) arterial phase hyperenhancement (arrow) and washout and capsule (not shown), categorized as LI-RADS 5. (B) MRI arterial phase scan 1 month after transarterial radioembolization, with an α-fetoprotein level of 12.5 ng/mL, shows minimal residual intralesional enhancement (11 o’clock position) and smooth perilesional rim enhancement (arrow), yielding LR-TR Nonprogressing. (C) On the MRI arterial phase scan 5 months after transarterial radioembolization, the treatment cavity was smaller, with decreasing intralesional enhancement and smooth perilesional rim enhancement (arrow), yielding LR-TR Nonprogressing. (D) On the MRI arterial phase scan 18 months after transarterial radioembolization, there was no residual intralesional enhancement, and the treatment cavity had decreased in size (arrow), yielding LR-TR Nonviable. Note the overlying capsular retraction from radiation fibrosis, an expected finding after transarterial radioembolization.
Liver Imaging Reporting and Data System treatment response (LR-TR)
Nonprogressing. MRI arterial phase scan in a 74-year-old male patient with
history of right segmentectomy for hepatocellular carcinoma, presenting with
a new 1.4-cm observation in the caudate, shows (A) arterial phase
hyperenhancement (arrow); washout was also observed (not shown). (B) MRI
arterial phase scan 3 months after stereotactic body radiation therapy shows
persistent irregular masslike enhancement of the treated lesion with
associated parenchymal perfusional enhancement (arrow), yielding LR-TR
Nonprogressing. (C) MRI arterial phase 6-month follow-up scan shows
decreasing size and enhancement of the treated observation with surrounding
parenchymal perfusional changes (arrow), consistent with expected
postradiation fibrosis, yielding LR-TR Nonprogressing. (D) MRI arterial
phase 12-month follow-up scan shows progressive atrophy of caudate with no
intralesional enhancement (arrow), yielding LR-TR Nonviable.
Figure 9:
Liver Imaging Reporting and Data System treatment response (LR-TR) Nonprogressing. MRI arterial phase scan in a 74-year-old male patient with history of right segmentectomy for hepatocellular carcinoma, presenting with a new 1.4-cm observation in the caudate, shows (A) arterial phase hyperenhancement (arrow); washout was also observed (not shown). (B) MRI arterial phase scan 3 months after stereotactic body radiation therapy shows persistent irregular masslike enhancement of the treated lesion with associated parenchymal perfusional enhancement (arrow), yielding LR-TR Nonprogressing. (C) MRI arterial phase 6-month follow-up scan shows decreasing size and enhancement of the treated observation with surrounding parenchymal perfusional changes (arrow), consistent with expected postradiation fibrosis, yielding LR-TR Nonprogressing. (D) MRI arterial phase 12-month follow-up scan shows progressive atrophy of caudate with no intralesional enhancement (arrow), yielding LR-TR Nonviable.

References

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