Clinicopathologic and Prognostic Differences Between LI-RADS M Targetoid and LI-RADS M Nontargetoid Observations: A
Indira Laothamatas1, Simon Gauvin1, Luke Ginocchio1
1Department of Radiology, NYU Langone Health, New York, New York, USA.
Journal of Magnetic Resonance Imaging : JMRI
|February 26, 2026
Summary
Targetoid lesions in Liver Imaging Reporting and Data System M (LR-M) indicate better survival and slower progression compared to nontargetoid lesions. This imaging feature can serve as a valuable prognostic biomarker for liver disease.
Area of Science:
- Radiology
- Oncology
- Hepatology
Background:
- Liver Imaging Reporting and Data System M (LR-M) lesions can be classified as targetoid or nontargetoid.
- The clinical, pathological, and prognostic distinctions between these two lesion types are not well understood.
Purpose of the Study:
- To compare the clinical, pathological, and prognostic characteristics of targetoid versus nontargetoid LR-M lesions using dynamic contrast-enhanced MRI (DCE-MRI).
Main Methods:
- A retrospective analysis of 119 LR-M observations in 119 patients with at least two years of follow-up.
- Lesions were categorized as targetoid or nontargetoid by three radiologists.
- Statistical analyses included t-tests, chi-square/Fisher's exact tests, Kaplan-Meier survival analysis, and Cox proportional hazards regression with IPTW.
Main Results:
- Nontargetoid lesions were associated with significantly higher serum AFP, larger size, and more frequent cirrhosis, extrahepatic disease, and malignancy.
- The nontargetoid group exhibited higher mortality and progression rates, with shorter overall survival and time-to-progression.
- Multivariable analysis revealed targetoid morphology as a significant predictor of improved overall survival (HR=0.28) and progression-free survival (HR=0.36).
Conclusions:
- Targetoid morphology in LR-M lesions is a significant indicator of improved patient survival and delayed disease progression.
- This imaging feature holds promise as a prognostic biomarker in liver disease management.

