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. 2017 Jul;6(3):167-170.
doi: 10.1159/000464285. Epub 2017 Mar 14.

Tremelimumab-Induced Graves Hyperthyroidism

Affiliations

Tremelimumab-Induced Graves Hyperthyroidism

Earn H Gan et al. Eur Thyroid J. 2017 Jul.

Abstract

Tremelimumab and ipilimumab are monoclonal antibodies directed against the extracellular domain of cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) and have been used as immunotherapies against immune checkpoints that suppress T-cell activation. Anti-CTLA-4 antibody-based therapies have been shown to be effective in treating various cancers including metastatic melanoma. However, a few immune-related adverse events including hypophysitis and thyroid disorder have been reported, mostly developed within the first year of receiving treatment. We report a case of tremelimumab-induced Graves hyperthyroidism in a 55-year-old man who was diagnosed with metastatic melanoma after 8 years of tremelimumab therapy. He had no personal or family history of thyroid or autoimmune diseases. His biochemical profile was in keeping with Graves disease, with raised serum free thyroid hormones, suppressed thyroid-stimulating hormone concentration, and raised thyrotropin receptor antibody level. He was treated with carbimazole as part of the block and replace therapy, without complications. Tremelimumab therapy was temporarily discontinued and recommenced when he was rendered biochemically euthyroid. There has been no further relapse of Graves hyperthyroidism since the discontinuation of block and replace therapy. The mechanistic profile of anti-CTLA-4-induced thyroid dysfunction and the long-term endocrine safety of this therapeutic approach remain unclear. It is important to monitor thyroid functions in patients receiving anti-CTLA-4 therapies, as their effects on endocrine systems could be more latent or prolonged than the data from current clinical trials suggest. Antithyroid drug therapy was safe and effective alongside anti-CTLA-4 therapy without compromising antitumour treatment efficacy.

Keywords: Graves disease; Hyperthyroidism; Tremelimumab.

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Figures

Fig. 1
Fig. 1
The time course of free T4, free T3, and TSH profiles from 12 months prior to the diagnosis of Graves disease to 6 months after the discontinuation of block and replace therapy (last clinic review). Shaded horizontal areas represent the normal range for the following thyroid parameters: TSH (0.3–4.7 mU/L), free T4 (9.5–21.5 pmol/L), free T3 (3.5–6.5 pmol/L).

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