4.7 Article

Induction of Painless Thyroiditis in Patients Receiving Programmed Death 1 Receptor Immunotherapy for Metastatic Malignancies

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 100, Issue 5, Pages 1738-1741

Publisher

ENDOCRINE SOC
DOI: 10.1210/jc.2014-4560

Keywords

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Funding

  1. Abbott Laboratories Limited Canada
  2. Da Vinci Gala Fundraiser
  3. George Knudson Oakdale Pro-Am Charity Golf Tournament
  4. Department of Medicine Research Fund at Mount Sinai Hospital
  5. Mount Sinai Hospital Foundation of Toronto
  6. Alex and Simona Shnaider Research Chair in Thyroid Oncology

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Context: Immunotherapies against immune checkpoints that inhibit T cell activation [cytotoxic T lymphocyte antigen 4 (CTLA-4) and programmed cell death 1 (PD-1)] are emerging and promising treatments for several metastatic malignancies. However, the precise adverse effects of these therapies on thyroid gland function have not been well described. Case Description: We report on 10 cases of painless thyroiditis syndrome (PTS) from a novel etiology, following immunotherapy with anti-PD-1 monoclonal antibodies (mAb) during treatment for metastatic malignancies. Six patients presented with transient thyrotoxicosis in which thyrotropin binding inhibitory immunoglobulins (TBII) were absent for all, whereas four patients had evidence of positive antithyroid antibodies. All thyrotoxic patients required temporary beta-blocker therapy and had spontaneous resolution of thyrotoxicosis with subsequent hypothyroidism. Four patients presented with hypothyroidism without a detected preceding thyrotoxic phase, occurring 6-8 weeks after initial drug exposure. All of these patients had positive antithyroid antibodies and required thyroid hormone replacement therapy for a minimum of 6 months. Conclusions: Patients receiving anti-PD-1 mAb therapy should be monitored for signs and symptoms of PTS which may require supportive treatment with beta-blockers or thyroid hormone replacement. The anti-PD-1 mAb is a novel exogenous cause of PTS and provides new insight into the possible perturbations of the immune network that may modulate the development of endogenous PTS, including cases of sporadic and postpartum thyroiditis.

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