Division of Endocrinology and Metabolism, Department of Internal Medicine, College of Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea, Banpo-daero, Seocho-gu, 222, Seoul, Republic of Korea.
Division of Endocrinology and Metabolism, Department of Internal Medicine, College of Medicine, Uijeongbu St. Mary's Hospital, The Catholic University of Korea, Uijeongbu, Republic of Korea.
BMC Endocr Disord. 2022 Apr 4;22(1):89. doi: 10.1186/s12902-022-01004-8.
Immune checkpoint inhibitors (ICIs) cause thyroid immune-related adverse effects (irAEs). However, associations between each type of thyroid immune-related adverse effect (irAE) and the anti-tumor effect of ICI remains unknown. This study aimed to determine the effects of each type of thyroid dysfunction on patient survival.
Patients who initiated ICI treatment from January 2015 to December 2019 in Seoul St. Mary's Hospital were retrospectively analyzed. Thyroid dysfunction was classified into four types: newly developed overt or subclinical hypothyroidism, thyrotoxicosis, worsened hypothyroidism, and subclinical hyperthyroidism. Patients were divided into two groups according to the presence or absence of thyroid dysfunction.
Among the 191 patients, 64 (33.5%) developed thyroid irAEs. There was no significant difference in age, sex, or cancer type between the two groups. The overall survival in patients with thyroid irAEs was significantly higher than that in patients without thyroid irAEs (25 months vs. 18 months, respectively, p = 0.005). After adjusting for confounding factors, the hazard ratio for mortality in the thyroid irAE group compared to the no thyroid irAE group was 0.480 (p = 0.006). Newly developed overt or subclinical hypothyroidism patients showed a significantly lower hazard ratio for mortality of 0.324 (p = 0.002). Patients with thyrotoxicosis showed a worse hazard ratio for mortality than those without thyroid irAE, although the difference was not statistically significant.
It was verified that ICI treatment-induced thyroid dysfunction was associated with better survival, even in the real-world practice. Thus, endocrinologists should cooperate with oncologists to monitor patients treated with ICIs.
免疫检查点抑制剂(ICI)可引起甲状腺免疫相关不良反应(irAE)。然而,每种类型的甲状腺免疫相关不良反应(irAE)与 ICI 的抗肿瘤作用之间的关联尚不清楚。本研究旨在确定每种类型的甲状腺功能障碍对患者生存的影响。
回顾性分析了 2015 年 1 月至 2019 年 12 月在首尔圣玛丽医院接受 ICI 治疗的患者。甲状腺功能障碍分为四种类型:新发生的显性或亚临床甲状腺功能减退症、甲状腺毒症、甲状腺功能减退恶化和亚临床甲状腺功能亢进症。根据是否存在甲状腺功能障碍,患者分为两组。
在 191 名患者中,64 名(33.5%)发生了甲状腺 irAE。两组患者的年龄、性别或癌症类型无显著差异。有甲状腺 irAE 的患者的总体生存率明显高于无甲状腺 irAE 的患者(分别为 25 个月和 18 个月,p=0.005)。在调整混杂因素后,与无甲状腺 irAE 组相比,甲状腺 irAE 组的死亡风险比为 0.480(p=0.006)。新发生的显性或亚临床甲状腺功能减退症患者的死亡风险比显著降低,为 0.324(p=0.002)。甲状腺毒症患者的死亡风险比无甲状腺 irAE 患者差,但差异无统计学意义。
证实 ICI 治疗引起的甲状腺功能障碍与更好的生存相关,即使在真实世界的实践中也是如此。因此,内分泌学家应与肿瘤学家合作,监测接受 ICI 治疗的患者。