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.
Authors
- Yaw Chyn Lim (ORCID: https://orcid.org/0000-0002-8919-0001)
- Li Ren Kong (ORCID: https://orcid.org/0000-0001-7980-4666)
- Boon Cher Goh (ORCID: https://orcid.org/0000-0002-4107-102X)
- Samantha Peiling Yang (ORCID: https://orcid.org/0000-0003-0838-6721)
- Regina Tong Xin Wong
- Wei Ming Chua (ORCID: https://orcid.org/0000-0002-2021-3586)
- Kelvin Siu Hoong Loke (ORCID: https://orcid.org/0000-0002-5339-5435)
- Lingzhi Wang (ORCID: https://orcid.org/0000-0001-5585-5426)
- David Chee Eng Ng (ORCID: https://orcid.org/0000-0001-8554-3036)
- Wan Qin Chong (ORCID: https://orcid.org/0000-0003-4012-6858)
- Min En Nga (ORCID: https://orcid.org/0000-0001-5592-6044)
- Young Soon Tay
- Belinda Wei Lin. Loh (ORCID: https://orcid.org/0009-0008-7904-4175)
Institutions
- 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)
Publication Details
- 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
- Type
- article
- Field-Weighted Citation Impact
- 0.00