Induction of painless thyroiditis in patients receiving programmed death 1 receptor immunotherapy for metastatic

Steven Orlov1, Farnaz Salari, Lawrence Kashat

  • 1Department of Medicine (S.O., F.S., L.K., P.G.W.), Endocrine Division, and Otolaryngology-Head and Neck Surgery Program (P.G.W.), Mt. Sinai Hospital, Toronto, ON M5G 1X5, Canada and University of Toronto School of Medicine, Toronto, ON M5S 1A8, Canada.

Abstract

Insights

Anti-PD-1 immunotherapy can cause painless thyroiditis syndrome (PTS), leading to temporary thyrotoxicosis or hypothyroidism. Patients require monitoring and potential treatment with beta-blockers or thyroid hormone replacement.

Area of Science:

  • Oncology
  • Immunology
  • Endocrinology

Background:

  • Immune checkpoint inhibitors, including cytotoxic T lymphocyte antigen 4 (CTLA-4) and programmed cell death 1 (PD-1) therapies, are effective treatments for metastatic malignancies.
  • Adverse effects of these immunotherapies on thyroid function are not well-characterized.

Purpose of the Study:

  • To describe cases of painless thyroiditis syndrome (PTS) in patients treated with anti-PD-1 monoclonal antibodies (mAb).
  • To investigate the clinical presentation and management of immunotherapy-induced thyroid dysfunction.

Main Methods:

  • Retrospective case series of 10 patients treated with anti-PD-1 mAb for metastatic malignancies.
  • Analysis of clinical presentation, thyroid function tests, antibody status, and treatment outcomes.

Main Results:

  • Six patients experienced transient thyrotoxicosis (absent thyrotropin binding inhibitory immunoglobulins) followed by hypothyroidism.
  • Four patients presented with hypothyroidism (positive antithyroid antibodies) without a preceding thyrotoxic phase.
  • All patients required supportive care, including beta-blockers or thyroid hormone replacement.

Conclusions:

  • Anti-PD-1 mAb therapy is a novel cause of painless thyroiditis syndrome (PTS).
  • Monitoring for PTS and prompt supportive treatment are crucial for patients receiving anti-PD-1 mAb therapy.
  • These findings offer insights into the immune network's role in endogenous PTS development.

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