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Theranostic role of radiolabelled RGD peptide in the treatment of radioiodine-resistant thyroid cancer: A novel agent
*For correspondence: sood99@yahoo.com
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This article was originally published by Wolters Kluwer - Medknow and was migrated to Scientific Scholar after the change of Publisher.
A 47 yr old female†, a known case of papillary carcinoma thyroid, post-total thyroidectomy and radioiodine treatment (I-131, cumulative dose of 716 mCi), presented to the department of Nuclear Medicine, Postgraduate Institute of Medical Education & Research, Chandigarh, India, in June 2019, with rising serum thyroglobulin (Tg) level of 13,840 ng/ml and anti-Tg of 34.53 IU/ml. Ultrasonography of the neck revealed a lobulated heterogeneous soft tissue mass in the midline and supraclavicular region, along with bilateral subcentimetric cervical lymph nodes. There was markedly elevated serum Tg and negative whole-body radioiodine scan, also known as TENIS (Thyroglobulin Elevation with Negative Iodine Scintigraphy) syndrome (Fig. 1). The patient was evaluated with whole-body gallium-68 (Ga-68) RGD positron emission tomography/computed tomography imaging (Fig. 2) for the staging and tumour tracer avidity for therapeutic potential with radionuclide therapy. RGD is an arginine–glycine–aspartic acid-based synthetic peptide targeting integrin αvβ3, which are overexpressed on endothelial cells of neovasculature and tumour cells. Lutetium-177 (Lu-177) RGD (~120 mCi) radionuclide therapy was given to the patient in view of tracer avidity in the residual/recurrent disease, and post-therapy images showed effective localization of tracer (Fig. 3). Lu-177 RGD may be a novel approach of treatment for radioiodine refractory thyroid cancer patients. Followup of the patient after four weeks of therapy showed significant reduction in serum Tg level from 13,840 ng/ml to 5,280 ng/ml with significant clinical improvement. The patient was planned for the second dose of Lu-177 RGD radionuclide therapy in view of favourable response.



Conflicts of Interest: None.