Auto-immune thyroid dysfunction induced by tyrosine kinase inhibitors in a patient with recurrent chordoma

BMC Cancer. 2016 Aug 24;16(1):679. doi: 10.1186/s12885-016-2705-3.

Abstract

Background: While hypothyroidism has frequently been reported with the use of TKIs, the thyroid-stimulating hormone (TSH) suppressing effect of TKIs is rare, except for thyroiditis. We describe a case with progressive recurrent chordoma who initially became hyperthyroid in a context of autoimmunity under sorafenib treatment and later under imatinib treatment.

Case presentation: A 57-year-old man with lumbar chordoma began daily treatment of 800 mg sorafenib. He did not have any other medication or recent iodinated-contrast exposure and his family history was negative for thyroid and autoimmune disease. There was no history of neck pain, irradiation or trauma, recent fever or viral illness. Pre-treatment TSH was normal. After 18 weeks of treatment, the patient presented hyperthyroidism with positive anti-TSH receptor antibodies. More surprisingly, Graves' disease recurred during treatment with imatinib.

Conclusion: The fact that Graves' disease occurred after two different TKIs suggests that it could be a rare but important class effect. Anti-TSH receptor antibodies should be systematically measured when TSH decreases in order to avoid the erroneous diagnosis of transient hyperthyroidism due to thyroiditis.

Keywords: Auto-immune thyroid dysfunction; Chordoma; Tyrosine kinase inhibitors.

Publication types

  • Case Reports

MeSH terms

  • Antineoplastic Agents / adverse effects
  • Chordoma / drug therapy*
  • Graves Disease / chemically induced*
  • Humans
  • Imatinib Mesylate / adverse effects*
  • Male
  • Middle Aged
  • Neoplasm Recurrence, Local / drug therapy
  • Niacinamide / adverse effects
  • Niacinamide / analogs & derivatives*
  • Phenylurea Compounds / adverse effects*
  • Protein Kinase Inhibitors / adverse effects*
  • Sorafenib

Substances

  • Antineoplastic Agents
  • Phenylurea Compounds
  • Protein Kinase Inhibitors
  • Niacinamide
  • Imatinib Mesylate
  • Sorafenib