# The Role of 123I in the Management of Differentiated Thyroid Cancer: A Comprehensive Narrative Review

**Authors:** Pietro Bellini, Francesco Dondi, Michela Cossandi, Gianluca Viganò, Carlo Cappelli, Elisa Gatta, Davide Lombardi, Riccardo Morandi, Claudio Casella, Luigi Spiazzi, Carlo Rodella, Federica Saiani, Chiara Ingraito, Valentina Zilioli, Francesco Bertagna

PMC · DOI: 10.3390/medsci14010068 · Medical Sciences · 2026-02-02

## TL;DR

This review discusses the use of 123I in diagnosing and managing differentiated thyroid cancer, highlighting its benefits and limitations compared to 131I.

## Contribution

The paper provides a comprehensive analysis of 123I's role in pre-treatment assessment and dosimetry for DTC.

## Key findings

- 123I scintigraphy is valuable for pre-treatment imaging in DTC patients.
- 123I has lower sensitivity than 131I for detecting metastatic lesions in lymph nodes and lungs.
- 123I may outperform low-dose 131I in some cases due to the absence of stunning.

## Abstract

Differentiated thyroid carcinoma (DTC) is the most common malignant endocrine tumor, with a generally favorable prognosis. Imaging, including iodine radioactive isotope scintigraphy (IRIS), is crucial for diagnosis and follow-up. While 131I has long been used for both therapeutic and diagnostic purposes, 123I is reserved for diagnostic imaging due to its shorter half-life and γ emissions. This review highlights the utility of 123I scintigraphy, especially in pre-treatment assessment and dosimetry for DTC. It is particularly valuable before radioiodine (RAI) ablation, providing accurate imaging in patients with iodine-refractory (IR) or biochemically incomplete response (BIR) DTC. When compared to post-therapeutic 131I scans, 123I scintigraphy appears to have a lower sensitivity for detecting metastatic lesions, particularly in lymph nodes and lungs. However, its diagnostic performance compared to low-dose diagnostic 131I is more variable, with some studies suggesting superiority due to the absence of stunning. Further research is needed to standardize its use and optimize its role in guiding DTC management.

## Linked entities

- **Chemicals:** 123I (PubChem CID 135300), 131I (PubChem CID 5489939)
- **Diseases:** differentiated thyroid carcinoma (MONDO:0015447)

## Full-text entities

- **Genes:** TG (thyroglobulin) [NCBI Gene 7038] {aka AITD3, TGN}, TERT (telomerase reverse transcriptase) [NCBI Gene 7015] {aka CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, SLC25A6 (solute carrier family 25 member 6) [NCBI Gene 293] {aka AAC3, ANT, ANT 2, ANT 3, ANT3, ANT3Y}
- **Diseases:** IR (MESH:D003409), ER (MESH:D018746), lung lesion (MESH:D008171), malignant tumor (MESH:D009369), metastatic disease (MESH:D000092182), nodal (MESH:D013611), RAI-avid disease (MESH:D004194), injury to (MESH:D014947), DTC metastases (MESH:D009362), DTC (MESH:D013964), hypothyroid (MESH:D007037), thyroid disease (MESH:D013959), lymph node involvement (MESH:D000072717), SIR (MESH:D020914), lymph-node metastases (MESH:D008207), reduction of kidney function (MESH:D007674), BIR (MESH:C536298), endocrine tumor (MESH:D004701), constipation (MESH:D003248)
- **Chemicals:** 131I (MESH:C000614965), 124I (MESH:C000614959), 18F-FDG (MESH:D019788), selumetinib (MESH:C517975), 123I Scan (-), 123I (MESH:C000614958), iodine (MESH:D007455)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12921828/full.md

## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC12921828/full.md

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Source: https://tomesphere.com/paper/PMC12921828