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Nivolumab-induced thyroid dysfunction lacking antithyroid antibody is frequently evoked in Japanese patients with malignant melanoma

Nivolumab, an anti-programmed cell death-1 monoclonal antibody, has improved the survival of patients with malignant melanoma. Despite its efficacy, nivolumab inconsistently induces thyroid dysfunction as an immune-related adverse event (irAE). This study aimed to evaluate nivolumab-induced thyroid...

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Published in:BMC endocrine disorders 2018-06, Vol.18 (1), p.36-36, Article 36
Main Authors: Yano, Seiichi, Ashida, Kenji, Nagata, Hiromi, Ohe, Kenji, Wada, Naoko, Takeichi, Yukina, Hanada, Yuki, Ibayashi, Yuta, Wang, Lixiang, Sakamoto, Shohei, Sakamoto, Ryuichi, Uchi, Hiroshi, Shiratsuchi, Motoaki, Furue, Masutaka, Nomura, Masatoshi, Ogawa, Yoshihiro
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Language:English
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Summary:Nivolumab, an anti-programmed cell death-1 monoclonal antibody, has improved the survival of patients with malignant melanoma. Despite its efficacy, nivolumab inconsistently induces thyroid dysfunction as an immune-related adverse event (irAE). This study aimed to evaluate nivolumab-induced thyroid dysfunction to determine the risks and mechanisms of thyroid irAEs. After excluding 10 patients, data of 24 patients with malignant melanoma (aged 17-85 years; 54% female) were retrospectively analyzed. Thyroid irAEs were observed in seven patients (29%). Three patients had hypothyroidism after preceding transient thyrotoxicosis, and the other four patients had hypothyroidism without thyrotoxicosis. Levothyroxine-Na replacement was required in three patients. Antithyroid antibody (ATA) titer was elevated in one of four assessable patients. The average (±SD) time to onset of thyroid irAE was 33.6 (±21.9) weeks. The administration period of nivolumab was longer in patients with thyroid irAEs than in those without thyroid irAEs (P 
ISSN:1472-6823
1472-6823
DOI:10.1186/s12902-018-0267-x