Kinetics of Re-differentiation with Short-Course Dabrafenib and Trametinib in Patients with Radioiodine-Refractory Thyroid Cancer

PURPOSE: MAPK pathway activation suppresses iodine-handling genes, including sodium-iodide symporter (NIS), contributing to loss of iodine avidity in radioiodine-refractory thyroid cancer. Prior BRAF/ MEK inhibitor re-differentiation trials improved iodine uptake but used empiric 4-6 week treatment. The timing of maximal NIS re-expression remains undefined. We evaluated whether short course dabrafenib plus trametinib restores iodine uptake and provides clinical benefit. PATIENTS AND METHODS: In this multicentre phase II trial, patients with progressive metastatic radioiodine-refractory thyroid carcinoma harbouring BRAFV600E or RAS mutations received dabrafenib and trametinib. I-124 PET/CT dosimetry was performed at baseline and after 2 weeks, with repeat imaging at week 4 post therapy if dosimetry criteria was not met. Radioiodine was administered once criteria was met. The primary endpoint was attainment of predicted lesional absorbed dose ≥20 Gy with I-131 activity ≤300 mCi. Secondary endpoints included RECIST response, progression-free survival (PFS), thyroglobulin response, and safety. RESULTS: Nine of 14 patients (64%) met the dosimetry criteria and received radioiodine; 6 out of 9 (67%) restored iodine uptake within 2 weeks. Among radioiodine-treated patients, best objective response rate within 6 months was 75% by RECIST. Median PFS was 10.8 months. RAS-mutant tumours demonstrated greater lesion regression than BRAFV600E-mutant tumours. Early reduction in stimulated thyroglobulin and preserved FOXE1 nuclear localisation, and higher tumour-to-normal GLIS3 nuclear expression were associated with re-differentiation response. CONCLUSIONS: Short-course dabrafenib/ trametinib can induce rapid re-differentiation within 2 weeks in a subset of patients with MAPK-driven radioiodine-refractory thyroid cancer, supporting individualized BRAF/MEK inhibition duration rather than empiric prolonged treatment.

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Journal
Clinical Cancer Research
Published
2026-11-09
DOI
https://doi.org/10.1158/1078-0432.ccr-26-2415
Primary Topic
Thyroid Cancer Diagnosis and Treatment
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article
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article

Kinetics of Re-differentiation with Short-Course Dabrafenib and Trametinib in Patients with Radioiodine-Refractory Thyroid Cancer

Yaw Chyn Lim, Li Ren Kong, Boon Cher Goh, Samantha Peiling Yang et al.
Clinical Cancer Research
Thyroid Cancer Diagnosis and Treatment
article

Kinetics of Re-differentiation with Short-Course Dabrafenib and Trametinib in Patients with Radioiodine-Refractory Thyroid Cancer

Yaw Chyn Lim, Li Ren Kong, Boon Cher Goh, Samantha Peiling Yang, Regina Tong Xin Wong, Wei Ming Chua, Kelvin Siu Hoong Loke, Lingzhi Wang, David Chee Eng Ng, Wan Qin Chong, Min En Nga, Young Soon Tay, Belinda Wei Lin. Loh
article en

Abstract

PURPOSE: MAPK pathway activation suppresses iodine-handling genes, including sodium-iodide symporter (NIS), contributing to loss of iodine avidity in radioiodine-refractory thyroid cancer. Prior BRAF/ MEK inhibitor re-differentiation trials improved iodine uptake but used empiric 4-6 week treatment. The timing of maximal NIS re-expression remains undefined. We evaluated whether short course dabrafenib plus trametinib restores iodine uptake and provides clinical benefit. PATIENTS AND METHODS: In this multicentre phase II trial, patients with progressive metastatic radioiodine-refractory thyroid carcinoma harbouring BRAFV600E or RAS mutations received dabrafenib and trametinib. I-124 PET/CT dosimetry was performed at baseline and after 2 weeks, with repeat imaging at week 4 post therapy if dosimetry criteria was not met. Radioiodine was administered once criteria was met. The primary endpoint was attainment of predicted lesional absorbed dose ≥20 Gy with I-131 activity ≤300 mCi. Secondary endpoints included RECIST response, progression-free survival (PFS), thyroglobulin response, and safety. RESULTS: Nine of 14 patients (64%) met the dosimetry criteria and received radioiodine; 6 out of 9 (67%) restored iodine uptake within 2 weeks. Among radioiodine-treated patients, best objective response rate within 6 months was 75% by RECIST. Median PFS was 10.8 months. RAS-mutant tumours demonstrated greater lesion regression than BRAFV600E-mutant tumours. Early reduction in stimulated thyroglobulin and preserved FOXE1 nuclear localisation, and higher tumour-to-normal GLIS3 nuclear expression were associated with re-differentiation response. CONCLUSIONS: Short-course dabrafenib/ trametinib can induce rapid re-differentiation within 2 weeks in a subset of patients with MAPK-driven radioiodine-refractory thyroid cancer, supporting individualized BRAF/MEK inhibition duration rather than empiric prolonged treatment.

Clinical Cancer Research
National University of Singapore (SG), Nanyang Technological University (SG), Singapore General Hospital (SG), National University Cancer Institute, Singapore (SG), National University Hospital (SG), Cancer Science Institute of Singapore (SG)
Thyroid Cancer Diagnosis and Treatment
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