Abstract
BackgroundLutetium 177 (177Lu) - DOTATATE is a form of peptide receptor radionuclide therapy (PRRT) utilized in the treatment of neuroendocrine tumors. Data on 177Lu-DOTATATE-induced thyroid dysfunction is limited.Case DescriptionA 29-year-old male with SDHB positive metastatic paraganglioma enrolled under the 177Lu-DOTATATE trial (NCT03206060) underwent thyroid function test (TFT) evaluation comprised of thyroid stimulating hormone (TSH) and free thyroxine (FT4) immunoassay measurements per protocol prior to 177Lu-DOTATATE therapy. The TSH was suppressed [<0.01 µIU/ml (0.27–4.2 µIU/ml)], and FT4 was normal [1.3 ng/dl (0.9–1.7 ng/dl)]. The TSH receptor antibody and thyroid stimulating immunoglobulin index were undetectable [<1 IU/L (≤1.75 IU/L), and <1 (≤1.3) respectively], while the anti-thyroid peroxidase (anti-TPO) and anti-thyroglobulin (anti-Tg) antibodies were elevated [605 IU/ml (0.0–34.9 IU/ml), and 178 IU/ml (0.0-40.0 IU/ml) respectively]. Mass spectrometry on a stored (-80°C) plasma sample obtained one-month pre-PRRT revealed elevated total triiodothyronine (TT3) [235 ng/dl (65–193 ng/dl)] and FT4 [3.9 ng/dl (1.2–2.9 ng/dl)] levels. The patient was diagnosed with Hashimoto’s thyrotoxicosis. However, the patient was asymptomatic. One month after the first dose of 200mCi 177Lu-DOTATATE, the patient noted fatigue and a 2.6 Kg weight gain. The TSH (73.04 µIU/ml), anti-TPO antibodies (>1,000 IU/ml), and anti-Tg antibodies (668 IU/ml) had substantially increased, with reductions in FT4 (0.3 ng/dl) and TT3 [54 ng/dl (87–169 ng/dl)]. Diagnostic gallium 68 - DOTATATE positron emission tomography-computed tomography performed prior to 177Lu-DOTATATE treatment revealed diffuse thyroid uptake. Post-therapy single-photon emission computed tomography also revealed diffuse uptake of 177Lu-DOTATATE in the thyroid gland. Levothyroxine therapy was initiated, and the patient’s symptoms resolved.SummaryWe report, for the first time, a patient with asymptomatic primary hyperthyroidism who rapidly developed symptomatic primary hypothyroidism 1 month after 177Lu-DOTATATE therapy, accompanied by marked changes in TFTs and thyroid auto-antibody titers, with functional imaging evidence of diffuse uptake of 177Lu-DOTATATE in the thyroid gland.ConclusionsThyroid dysfunction can be associated with PRRT. Thyroid uptake patterns on pre-treatment diagnostic somatostatin analog scans might predict individual susceptibility to PRRT-associated TFT disruption. Therefore, periodic evaluation of TFTs should be considered in patients receiving PRRT.
Highlights
Peptide receptor radionuclide therapy (PRRT) is a form of targeted therapy that has demonstrated substantial efficacy in the treatment of neuroendocrine tumors (NETs) [1, 2]
Lutetium 177 (177Lu) - DOTA-DPhe1, Tyr3-octreotate (DOTATATE) (Lutathera®, Advanced Accelerator Applications, Saint-Genis-Pouilly, France) is a form of PRRT with the highest affinity to SSTR-2. It has been successfully utilized in treating gastroenteropancreatic NETs and was recently shown to markedly prolong progression-free survival among patients with advanced, well-differentiated midgut NETs in the NETTER-1 phase 3 trial [2]. This agent has demonstrated substantial safety and efficacy based on data from 1200 patients treated for gastroenteropancreatic and bronchial NETs [5]. 177LuDOTATATE has been effectively utilized in the treatment of inoperable, metastatic pheochromocytomas and paragangliomas (PPGLs) [6, 7]. 177Lu radionuclide exerts its anti-tumor effects by emitting medium energy beta particles and has a maximal tissue penetration of 2 mm [8]. 177Lu-DOTATATE therapy is associated with several adverse effects, with nausea and vomiting being the most common adverse effects
For the first time, a patient with primary hyperthyroidism who rapidly progressed to primary hypothyroidism after the first dose of 177Lu-DOTATATE therapy
Summary
Lutetium 177 (177Lu) - DOTATATE is a form of peptide receptor radionuclide therapy (PRRT) utilized in the treatment of neuroendocrine tumors. The TSH receptor antibody and thyroid stimulating immunoglobulin index were undetectable [
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