Department of Endocrinology, The 3rd Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Department of Endocrinology, Affiliated Hospital of Hebei University, Baoding, Hebei, China.
Clin Endocrinol (Oxf). 2024 Aug;101(2):130-139. doi: 10.1111/cen.15075. Epub 2024 May 16.
We aimed to elucidate the clinical features of pituitary immune-related adverse events (irAEs) induced by PD-1 inhibitors in a Chinese cohort and the previous literatures.
We retrospectively analysed the clinical manifestations, laboratory examination findings, imaging features and treatments of 14 patients with pituitary irAEs caused by PD-1 inhibitors in our cohort. In addition, we searched PubMed for all English articles on pituitary irAEs induced by PD-1 inhibitors published from 1950 to 2023. A total of 47 articles were included, and the clinical characteristics of 94 patients with pituitary irAEs induced by PD-1 inhibitors in these literatures were compared to the characteristics of our cohort.
Among the 14 patients in our cohort with pituitary irAEs induced by PD-1 inhibitors, 12 patients (85.71%, 12/14) exhibited isolated ACTH deficiency (IAD), 100.0% (14/14) of the central adrenocortical insufficiency, and 2 patients showed more than one hypothalamic-pituitary axis injury (14.29%, 2/14). Pituitary magnetic resonance imaging in all the 14 patients showed no pituitary enlargement. In previous studies we reviewed, 82.98% of the total (78/94) presented with pituitary irAEs as IAD, 100.0% (94/94) of the central adrenocortical insufficiency, and 78.33% of the patients showed no abnormality of the pituitary gland (47/60). The pituitary irAEs caused by PD-1 inhibitors did not involve typical manifestations of hypophysitis, such as pituitary enlargement, headache, visual field defects, and multiple pituitary function impairments in our cohort and the previous literatures.
In our study, pituitary immune-related adverse reactions induced by PD-1 inhibitors mainly manifested isolated ACTH deficiency rather than hypophysitis.
我们旨在阐明中国人群中 PD-1 抑制剂诱导的垂体免疫相关不良事件(irAEs)的临床特征,并对既往文献进行综述。
我们回顾性分析了 14 例来自本队列的 PD-1 抑制剂诱导的垂体 irAEs 患者的临床表现、实验室检查结果、影像学特征和治疗方法。此外,我们在 PubMed 上搜索了 1950 年至 2023 年发表的所有关于 PD-1 抑制剂诱导的垂体 irAEs 的英文文章。共纳入 47 篇文章,比较了这些文献中 94 例 PD-1 抑制剂诱导的垂体 irAEs 患者的临床特征与本队列的特征。
在我们的队列中,14 例 PD-1 抑制剂诱导的垂体 irAEs 患者中,12 例(85.71%,12/14)表现为单纯 ACTH 缺乏症(IAD),100.0%(14/14)存在中枢肾上腺皮质功能不全,2 例患者表现为多种下丘脑-垂体轴损伤(14.29%,2/14)。所有 14 例患者的垂体磁共振成像均未见垂体肿大。在我们回顾的既往研究中,总共有 82.98%(78/94)的患者表现为 IAD 型垂体 irAEs,100.0%(94/94)的患者存在中枢肾上腺皮质功能不全,78.33%(47/60)的患者垂体未见异常。在我们的队列和既往文献中,PD-1 抑制剂引起的垂体 irAEs 并不涉及典型的垂体炎表现,如垂体肿大、头痛、视野缺损和多种垂体功能不全。
在本研究中,PD-1 抑制剂诱导的垂体免疫相关不良反应主要表现为单纯 ACTH 缺乏症,而不是垂体炎。