Department of Pharmacy, Tianjin First Central Hospital, Tianjin, P.R. China.
J Chemother. 2024 Dec;36(8):654-661. doi: 10.1080/1120009X.2024.2305065. Epub 2024 Jan 19.
This study aimed to identify the potential factors associated with immune thyroid dysfunction caused by programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) inhibitors in cancer patients. We conducted a retrospective study of thyroid immune-related adverse events (irAEs) in cancer patients treated with PD-1/PD-L1 inhibitors at Tianjin First Central Hospital from January 2020 to March 2023. Thyroid irAEs were characterized as hypothyroidism, hyperthyroidism and thyrotoxicosis followed by hypothyroidism. A total of 175 patients were screened in the study, of whom 48 patients (27%) developed thyroid irAEs (including 24 hypothyroidism, 11 hyperthyroidism and 13 thyrotoxicosis followed by hypothyroidism) following PD-1/PD-L1 inhibitors treatment. Multivariate logistic regression analysis showed that combination therapy with PD-1/PD-L1 inhibitors and tyrosine kinase inhibitors (lenvatinib/regorafenib) and high baseline anti-TPO level were associated with the development of thyroid irAEs caused by PD-1/PD-L1 inhibitors. The nomogram models showed good discriminant ability and could bring net benefits for more patients according to the decision curve analysis. However, the model needs to be further validated in other large cohorts.
本研究旨在确定与癌症患者程序性死亡 1(PD-1)/程序性死亡配体 1(PD-L1)抑制剂引起的免疫性甲状腺功能障碍相关的潜在因素。我们对 2020 年 1 月至 2023 年 3 月在天津市第一中心医院接受 PD-1/PD-L1 抑制剂治疗的癌症患者的甲状腺免疫相关不良事件(irAE)进行了回顾性研究。甲状腺 irAE 表现为甲状腺功能减退症、甲状腺功能亢进症和甲状腺毒症后继发甲状腺功能减退症。本研究共筛选了 175 例患者,其中 48 例(27%)在接受 PD-1/PD-L1 抑制剂治疗后发生甲状腺 irAE(包括 24 例甲状腺功能减退症、11 例甲状腺功能亢进症和 13 例甲状腺毒症后继发甲状腺功能减退症)。多变量逻辑回归分析表明,PD-1/PD-L1 抑制剂联合酪氨酸激酶抑制剂(仑伐替尼/regorafenib)治疗和基线抗 TPO 水平高与 PD-1/PD-L1 抑制剂引起的甲状腺 irAE 发生相关。列线图模型显示出良好的判别能力,并且根据决策曲线分析可以为更多患者带来净收益。然而,该模型需要在其他大样本中进一步验证。