Evidence map›Paper›PMID 42804115›Full record

ArticleEndocrine2026

The impact of RET fusions on radioiodine avidity and prognosis in patients with distant metastatic papillary thyroid cancer.

Kexin Shi, Xinyue Zhang, Shuhui Huang, Tian Tian, Rui Huang

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Article in Endocrine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Kexin ShiDepartment of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu, China.
Xinyue ZhangDepartment of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu, China.
Shuhui HuangDepartment of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu, China.
Tian TianDepartment of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu, China. tiantianscu@stu.scu.edu.cn.
Rui HuangDepartment of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu, China. huang_rui@scu.edu.cn.ORCID http://orcid.org/0000-0003-3191-0528

Funding

1.3.5 project for disciplines of excellence, West China Hospital, Sichuan University 23HXFH025Science & Technology Department of Sichuan Province 2024YFFK0025Sichuan Province Nuclear Medicine Whole Industry Chain Breakthrough Project JG202507
6 · The paper itself

Abstract

backgroundRET gene fusion is one of the key oncogenic drivers in papillary thyroid cancer (PTC). However, the impact of different RET fusion subtypes on clinicopathological features and radioiodine (RAI) avidity in metastatic PTC remains unclear.

methodsWe retrospectively analyzed clinicopathological data, RAI avidity, and progression-free survival (PFS) in RET-driven metastatic PTC. Initial RAI avidity status was classified as initially RAI-avid (all or partial lesions showing uptake in the first therapy) or initially RAI-non-avid (all lesions with no uptake in the first therapy). The definition of RAI refractory (RAIR) was based on the 2025 ATA guidelines.

resultsAmong 65 enrolled patients, 25 (38.5%) harbored CCDC6-RET, 24 (36.9%) NCOA4-RET, and 16 (24.6%) other RET fusions. Older age was associated with the other RET fusion group (P = 0.011). NCOA4-RET patients were more likely to be initially RAI-avid (P = 0.017). Overall, 46.8% (29/62) of evaluable patients were classified as RAIR (CCDC6: 56.0%, NCOA4: 27.3%, other RET fusions: 60.0%; P = 0.072). TERT promoter mutation (18.2%, 8/44) in RET-fusion PTC was associated with older age (P < 0.001), larger metastatic lesions (P = 0.012) and metastatic sites beyond lungs (P = 0.002). RAIA patients demonstrated a longer median PFS compared with RAIR patients (86 vs. 33 months), but this association was not statistically significant (P = 0.402).

conclusionIn this metastatic RET-driven PTC cohort, 46.8% of evaluable patients eventually develop RAIR status. While the specific RET subtypes are associated with initial RAI avidity status, no significant differences in RAIR status or PFS were observed across distinct RET subtypes, warranting further exploration in larger sample sizes.

Indexed as

Iodine RadioisotopesOncogene Proteins, FusionProto-Oncogene Proteins c-retThyroid Cancer, PapillaryThyroid NeoplasmsAdultAgedFemaleHumansMaleMiddle AgedNeoplasm MetastasisNuclear Receptor CoactivatorsPrognosisRetrospective StudiesIodine RadioisotopesNCOA4 protein, humanNuclear Receptor CoactivatorsOncogene Proteins, FusionProto-Oncogene Proteins c-retRET protein, humanDistant metastasesPapillary thyroid cancerRadioiodine refractoryRET fusion

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.