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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.
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.
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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