What is the recommended dosing for Y90 (Yttrium-90) radioembolization?

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Last updated: August 31, 2025View editorial policy

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Y90 Radioembolization Dosing Recommendations

For optimal outcomes in Y90 radioembolization, personalized dosimetry with tumor-absorbed doses of at least 205 Gy should be delivered to the tumor, which significantly improves survival compared to standard dosing approaches. 1

Dosing Approaches and Considerations

Standard vs. Personalized Dosimetry

  • Standard dosing approach:

    • Traditional absorbed dose of 100-150 Gy to the perfused lobe 1
    • Associated with median survival of 10.7 months in BCLC stage B/C with tumors >7cm 1
  • Personalized dosimetry approach:

    • Delivers at least 205 Gy to the tumor 1
    • Associated with median survival of 26.6 months (compared to 10.7 months with standard dosing) 1
    • Higher radiation doses (>150 Gy) have shown complete remission rates of 80-84% 1

Specific Dosing Techniques

  1. Radiation Segmentectomy:

    • Delivers ablative doses >190 Gy to small segments containing early-stage HCC 2
    • Potential curative approach for early HCC
  2. Radiation Lobectomy:

    • Used for large tumors requiring extended hepatectomy 2
    • Induces contralateral liver hypertrophy while treating the tumor
    • Allows for future surgical resection
  3. Lobar Treatment:

    • Standard approach for multifocal disease within a lobe 2
    • Typically delivers 80-150 Gy to the target lobe

Pre-Treatment Assessment Requirements

  1. Mandatory Workup:

    • Diagnostic angiography with technetium-99m macroaggregated albumin (MAA) scan 2
    • Lung shunt fraction calculation to prevent radiation pneumonitis 1
    • Assessment for potential extrahepatic microsphere deposition 2
  2. Lung Dose Assessment:

    • Critical to prevent radiation pneumonitis 1
    • May be eliminated in patients with HCC within Milan criteria except those with transjugular intrahepatic portosystemic shunt 1

Patient Selection Factors Affecting Dosing

  • Liver Function:

    • Child-Pugh score and bilirubin levels 2
    • For cirrhotic patients, more conservative approaches may be needed
  • Tumor Characteristics:

    • Size: Higher doses (>150 Gy) for tumors ≥5 cm have shown 80% complete remission rates 1
    • Single vs. multifocal disease
  • Risk Factors for Radioembolization-Induced Liver Disease (REILD):

    • Small liver (<1.5 L) 1
    • Small functional liver volume associated with cirrhosis 1
    • Systemic therapy within 2 months 1
    • Extensive infusion to both liver lobes 1
    • Tumor involvement >50% of the liver 1

Dose-Response Relationship

Recent evidence demonstrates a clear dose-response relationship in Y90 radioembolization:

  • Responding tumors: mean absorbed dose of 170 Gy 3
  • Stable disease: mean absorbed dose of 101 Gy 3
  • Progressive disease: mean absorbed dose of 67 Gy 3

Based on this data, a minimum planned tumor-absorbed dose of 150 Gy is recommended 3

Implementation of Dosing

  1. Computational Approaches:

    • Personalized dosimetry using computational fluid dynamics and Monte Carlo simulation can optimize dose distribution 4
    • Post-treatment PET imaging at 2 hours can verify dose distribution 4
  2. Same-Day Protocol Option:

    • For select patients, planning angiography and treatment can be performed on the same day 5
    • Requires proper pre-procedure planning based on baseline imaging

Monitoring and Safety

  • Monitor for REILD, which typically occurs 4-8 weeks post-treatment 1
  • Delayed hepatotoxicity may occur up to 6 months after treatment 1
  • Common side effects include temporary fatigue (most common), nausea, and abdominal pain 6

Conclusion

Y90 radioembolization dosing should be personalized based on tumor characteristics and liver function. The evidence strongly supports using higher doses (>205 Gy) to the tumor when feasible, as this significantly improves survival outcomes compared to standard dosing approaches. Proper pre-treatment assessment, including lung shunt calculation and careful patient selection, is essential to minimize complications while maximizing therapeutic efficacy.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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