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Trans-arterial Radioembolization Dosimetry in 2022
Etienne Garin1, Boris Guiu2, Julien Edeline3
1Department of Nuclear Medicine, Centre de Lutte Contre le Cancer Eugène Marquis, 35042, Rennes, France. e.garin@rennes.unicancer.fr.
Cardiovascular and Interventional Radiology
|August 18, 2022
Summary
Personalized dosimetry for trans-arterial radioembolization (TARE) using yttrium-90 or holmium-166 microspheres improves patient outcomes. This approach is now a clinical standard for hepatocellular carcinoma (HCC) and colorectal cancer metastases.
Area of Science:
- Nuclear medicine
- Interventional radiology
- Oncology
Background:
- Trans-arterial radioembolization (TARE) uses yttrium-90 (90Y) or holmium-166 (166Ho) microspheres.
- Different microsphere types and isotopes have varying radiobiology, impacting effective tumoricidal doses.
Purpose of the Study:
- To review dosimetry and radiobiology concepts for TARE.
- To present dosimetry approaches, confounding factors, and clinical results over the past decade.
- To highlight the impact of personalized dosimetry on treatment outcomes.
Main Methods:
- Review of simulation-based and post-treatment dosimetry approaches.
- Analysis of clinical dosimetry results for hepatocellular carcinoma (HCC) and metastatic colorectal carcinoma (mCRC).
- Evaluation of tumoricidal and maximal tolerated doses for different TARE agents.
Main Results:
- Tumoricidal doses vary: 100-120 Gy (90Y resin), 205 Gy (90Y glass) for HCC; 39-60 Gy (90Y resin), 139 Gy (90Y glass), 90 Gy (166Ho) for mCRC.
- Tumor dose correlates with overall survival.
- Personalized dosimetry is increasingly recommended and supported by level-one evidence for HCC.
Conclusions:
- Personalized dosimetry is crucial for optimizing TARE efficacy.
- Evidence supports personalized dosimetry as a new standard for TARE in HCC.
- This approach impacts clinical practice, trial design, and patient survival.

