Department of Pharmacy, Ogaki Municipal Hospital, 4-86 Minaminokawa-cho, Ogaki-shi 503-8502, Gifu, Japan.
Laboratory of Clinical Pharmacy, Gifu Pharmaceutical University, 1-25-4 Daigakunishi, Gifu-shi 501-1196, Gifu, Japan.
Medicina (Kaunas). 2023 Nov 7;59(11):1963. doi: 10.3390/medicina59111963.
: One type of immune-related adverse event caused by immune checkpoint inhibitors (ICIs) is pituitary-related adverse events. The management of pituitary-related adverse events is important because they can be fatal if not treated promptly. Therefore, this study was conducted to investigate the onset of pituitary-related adverse events using the Japanese Adverse Drug Report (JADER) database. : Cases registered in the JADER database from 2004 to 2019 were used. The target drugs were ipilimumab, nivolumab, pembrolizumab, avelumab, atezolizumab, and durvalumab, and the target adverse events were the high-level terms "Anterior pituitary hypofunction," "Anterior pituitary hyperfunction," "Posterior pituitary disorder," and "Pituitary neoplasm" in the Medical Dictionary for Regulatory Activities, Japanese version (MedDRA/J). The information component (IC) was used for signal detection and IC delta (ICΔ) was used for women-related signals. Onset timing and patterns were analyzed using the Weibull distribution. : Signals were detected with ipilimumab, nivolumab, pembrolizumab, and atezolizumab in "Anterior pituitary hypofunction," with ICs and 95% credible intervals (95%CrI) of 5.53 (5.30-5.69), 4.96 (4.79-5.08), 4.04 (3.76-4.25), and 2.40 (1.53-3.00). Significant signals were detected in women, except for atezolizumab. Additionally, the time of onset was classified as the wear-out failure type. Inverse signals were detected with ipilimumab and nivolumab in "Posterior pituitary disorder," with ICs (95%CrI) of -1.24 (-2.80--0.26), and -0.89 (-1.64--0.37). : Anterior pituitary hypofunction is likely to occur with the long-term administration of ipilimumab, nivolumab, and pembrolizumab. Further investigation is needed to determine the differences in the tendencies to detect signals in the anterior and posterior pituitaries between ipilimumab and nivolumab.
免疫检查点抑制剂(ICIs)引起的一种免疫相关不良事件是垂体相关不良事件。由于如果不及时治疗,垂体相关不良事件可能致命,因此管理垂体相关不良事件非常重要。因此,本研究使用日本不良药物报告(JADER)数据库调查了垂体相关不良事件的发病情况。
使用了 2004 年至 2019 年在 JADER 数据库中注册的病例。靶药为伊匹单抗、纳武单抗、帕博利珠单抗、avelumab、阿替利珠单抗和度伐鲁单抗,靶不良事件为监管活动医学词典(MedDRA/J)中的高级术语“垂体前叶功能减退症”、“垂体前叶功能亢进症”、“垂体后叶紊乱”和“垂体肿瘤”。信息成分(IC)用于信号检测,女性相关信号使用 IC 差值(ICΔ)。使用威布尔分布分析发病时间和模式。
在“垂体前叶功能减退症”中,伊匹单抗、纳武单抗、帕博利珠单抗和阿替利珠单抗检测到信号,IC 和 95%可信区间(95%CrI)分别为 5.53(5.30-5.69)、4.96(4.79-5.08)、4.04(3.76-4.25)和 2.40(1.53-3.00)。除了阿替利珠单抗,女性中检测到了显著信号。此外,发病时间分类为耗竭失效型。在“垂体后叶紊乱”中,伊匹单抗和纳武单抗检测到反向信号,IC(95%CrI)分别为-1.24(-2.80--0.26)和-0.89(-1.64--0.37)。
长期使用伊匹单抗、纳武单抗和帕博利珠单抗可能导致垂体前叶功能减退症。需要进一步研究以确定伊匹单抗和纳武单抗在检测前、后垂体信号方面的趋势差异。