A 29-y-old woman requiring total thyroidectomy with lymph node dissection for a stage pT3(m)N1bMxR2 solid variant of papillary thyroid cancer had, near the left recurrent vagal nerve, a 16 × 10 × 8 mm cervical tumor residue deemed unresectable by expert surgeons. After hormone withdrawal, she received 3.7 GBq of 131I. Although a posttreatment scan showed no iodine uptake, [18F]FDG PET/CT revealed pathologic uptake in the tumor residue, indicating radioiodine refractoriness (Figs. 1A and 1B). An NCOA4-RET fusion transcript was identified.
During first radioiodine treatment, [18F]FDG PET/CT scan showed hypermetabolism in left cervical region due to tumor residue (green arrows) (A), and postradioiodine scan revealed right laterocervical (blue arrows) fixations with no uptake at tumor site (B). During second radioiodine treatment with selpercatinib, [18F]FDG PET/CT scan (C) and postradioiodine (D) scan showed [18F]FDG-negative, radioiodine-positive neck residue and metastatic miliary lung disease (green arrows).
Eight months later, the tumor size remained unchanged but the patient complained of dysphonia. Local and national ENDOCAN-TUTHYREF tumor boards suggested another radioiodine treatment after redifferentiation with a RET-selective inhibitor. Selpercatinib—obtained through compassionate access from Lilly, France—was administered for 6 wk. After levothyroxine withdrawal to optimize 131I uptake and residency, 3.7 GBq of radioiodine were delivered on day 35. Contrary to previous findings, [18F]FDG PET/CT showed no significant abnormality, whereas post–radioactive iodine scanning revealed intense uptake in the residual cervical tumor and mild, diffuse uptake in the lungs suggestive of infraradiologic metastatic disease (Figs. 1C and 1D). Eight months after redifferentiation, the thyroglobulin level was undetectable (vs. 6.94 ng/mL before selpercatinib treatment), dysphonia resolved, and further imaging indicated no abnormality.
Redifferentiation-facilitated radioactive iodine therapy is emerging as a new option in treating radioactive iodine–refractory thyroid cancer, particularly with BRAF (B-Raf protooncogene) and MEK (mitogen-activated protein kinase kinase) inhibitors (1). Selpercatinib has shown significant antitumor properties, with few observations of its use for redifferentiation (2,3). This case confirms the feasibility and efficacy of redifferentiation in RET fusion-positive thyroid cancer, achieving curative outcomes with the possibility to preserve the recurrent vagal nerve that would have been sacrificed in the case of surgery. We also report here, for the first time to our knowledge, a strategy using short sequential RET inhibition followed by radioiodine administration in line with an approved redifferentiation protocol with BRAF-MEK inhibitors. Such a schedule contrasts with previous similar experiences consisting mainly of radioiodine therapy given after a long period of selpercatinib treatment.
Our findings also suggest that selpercatinib can be safely administered with hormone withdrawal instead of recombinant human thyroid‐stimulating hormone, enhancing radioiodine efficacy and unmasking miliary lung disease.
DISCLOSURE
No potential conflict of interest relevant to this article was reported. The ENDOCAN-TUTHYREF network approved this work, and the patient gave written informed consent.
Footnotes
Published online Jan. 16, 2025.
- © 2025 by the Society of Nuclear Medicine and Molecular Imaging.
- Received for publication August 25, 2024.
- Accepted for publication January 6, 2025.