Temporal evolution of the LI-RADS radiation treatment response assessment on multiphase CT/MRI in patients undergoing selective internal radiation therapy for hepatocellular carcinoma - Scorecard - MDSpire

Temporal evolution of the LI-RADS radiation treatment response assessment on multiphase CT/MRI in patients undergoing selective internal radiation therapy for hepatocellular carcinoma

  • By

  • Hong Wei

  • Hanyu Jiang

  • Jeongin Yoo

  • Jae Hyun Kim

  • Hyo-Jin Kang

  • Yuanan Wu

  • Rongbo Liu

  • Hyo-Cheol Kim

  • Jeong Min Lee

  • May 17, 2025

  • 0 min

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Clinical Scorecard: Progression of LI-RADS Assessment for Radiation Treatment Response on Multiphase CT/MRI in Patients Receiving Selective Internal Radiation Therapy for Hepatocellular Carcinoma

At a Glance

CategoryDetail
ConditionHepatocellular carcinoma (HCC)
Key MechanismsSelective internal radiation therapy (SIRT) with Yttrium-90 induces gradual tumor response via DNA damage, free radical formation, and activation of proinflammatory and reparative pathways
Target PopulationAdult patients (≥18 years) with HCC, BCLC stage A-C without extrahepatic metastases, no prior HCC treatment, and suitable liver function
Care SettingMultidisciplinary liver cancer centers performing locoregional therapies with imaging follow-up

Key Highlights

  • SIRT is an emerging locoregional therapy for HCC with demonstrated clinical benefits and safety across early to intermediate stages
  • The 2024 LI-RADS CT/MRI Radiation Treatment Response Assessment (TRA) algorithm introduces a specific framework for evaluating radiation-based therapies including a new LR-TR nonprogressing category
  • Tumor response after SIRT evolves gradually over months, necessitating dynamic imaging evaluation at 3–6 months post-treatment for accurate assessment

Guideline-Based Recommendations

Diagnosis

  • Use LI-RADS version 2018 diagnostic algorithm for initial HCC diagnosis
  • Perform multiphase contrast-enhanced CT/MRI within 2 months before SIRT
  • Apply LI-RADS CT/MRI Radiation TRA version 2024 for treatment response assessment at 3–6 months post-SIRT

Management

  • Select patients for SIRT based on tumor burden (≤70% liver volume, single tumor ≤8 cm), liver function (Child–Pugh A or B7), performance status (ECOG 0 or 1), and patient preference
  • Conduct planning angiography with Tc-99m MAA mapping prior to SIRT for dosimetry and treatment planning
  • Administer Y90 glass or resin microspheres with personalized dosimetry sparing at least 30% of functional liver volume and limiting lung dose to 30 Gy

Monitoring & Follow-up

  • Perform multiphase CT/MRI at 3–6 months post-SIRT to evaluate treatment response using LI-RADS Radiation TRA categories
  • Assess imaging features including lesion size, masslike enhancement, lesion disappearance, perilesional enhancement, and ancillary MRI features favoring viability
  • Use dynamic and longitudinal imaging evaluation to identify treatment failure or progression

Risks

  • Avoid SIRT in patients with main portal vein tumor thrombosis or extensive liver involvement beyond criteria
  • Monitor for potential radiation-induced liver injury by sparing adequate functional liver volume and limiting lung radiation dose

Patient & Prescribing Data

Patients with HCC eligible for SIRT without prior treatment and adequate liver function

SIRT is administered selectively via segmental or lobar arteries using Y90 microspheres with personalized dosimetry; treatment response is gradual and requires imaging follow-up for accurate assessment

Clinical Best Practices

  • Use multidisciplinary tumor board discussions to select appropriate candidates for SIRT
  • Follow standardized imaging protocols per LI-RADS minimum technique specifications for CT and MRI
  • Ensure blinded, independent radiologist review of imaging to improve interobserver agreement in treatment response assessment
  • Incorporate the LR-TR nonprogressing category to better characterize stable or decreasing masslike enhancement lesions post-radiation therapy
  • Avoid retreatment within 12 months post-SIRT unless clear evidence of progression

References

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