Pre-Therapeutic Measurements of Iodine Avidity in Papillary and Poorly Differentiated Thyroid Cancer Reveal Associations with Thyroglobulin Expression, Histological Variants and Ki-67 Index

• Published in: Cancers Vol. 13; no. 14; p. 3627
• Main Authors: Nilsson, Joachim N., Siikanen, Jonathan, Hedman, Christel, Juhlin, C. Christofer, Ihre Lundgren, Catharina
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 20.07.2021; MDPI
• Subjects: Avidity; Biopsy; Cancer therapies; Cellular biology; differentiated thyroid cancer; Histopathology; Iodine; iodine avidity; Lymph nodes; Lymphatic system; Medical prognosis; Medicin och hälsovetenskap; Metastasis; Monoclonal antibodies; Papillary thyroid cancer; Pathology; Patients; poorly differentiated thyroid cancer; Prognosis; Radiation; Radioactivity; radioiodine therapy; Surgery; Thyroglobulin; Thyroid cancer; Tumors
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers13143627

Papillary thyroid cancer (PTC) and poorly differentiated thyroid cancer (PDTC) are treated with radioiodine to reduce recurrence and to treat the spread of disease. Adequate iodine accumulation in cancer tissue, iodine avidity, is important for treatment effect. This study investigated which clinical and histological tumour characteristics correlate with avidity. To quantify avidity in cancer tissue, tracer amounts of iodine-131 were given to 45 patients with cytologically confirmed thyroid cancer. At pathology grossing, representative samples of tumour and lymph nodes were taken and subjected to radioactivity quantification ex vivo to determine avidity. Afterwards, samples underwent extended pathology work-up and analysis. We found that tumoural Tg expression and Ki-67 index were correlated with avidity, whereas tumour size and pT stage were not. The histological variant of thyroid cancer was also correlated with iodine avidity. Variants associated with worse clinical prognoses displayed lower avidity than variants with better prognoses. This work provides new information on which tumours have low iodine avidity. Lower avidity in aggressive histological PTC variants may explain their overall poorer prognoses. Our findings also suggest that radioiodine dosage could be adapted to Tg expression, Ki-67 index or histological variant instead of pT stage, potentially improving the efficacy of radioiodine therapy.