Multiple or Single Endocrine Abnormalities Associated with Immune Checkpoint Inhibitors.

Fumika Kamitani, Yuichi Nishioka, Hiroki Nakajima, Yukako Kurematsu, Sadanori Okada, Tomoya Myojin, Tatsuya Noda, Tomoaki Imamura, Yutaka Takahashi
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Abstract

Background: Immune checkpoint inhibitors (ICIs) are associated with various endocrine abnormalities. However, their underlying pathophysiology remains unclear. We investigated the effect of multiple endocrine abnormalities on the overall survival (OS) of patients treated with ICIs.

Methods: In total, 12,978 patients who received ICIs between 2014 and 2022 were investigated using the DeSC Japanese administrative claims database. Endocrine abnormalities were defined by each hormone replacement therapy, including levothyroxine, hydrocortisone, and insulin, in which it is difficult to distinguish central or primary hormone defect. Also, only patients with hypothyroidism after thyroiditis were included. Type 1 diabetes was additionally defined by the name of the disease and strict self-injection fees. Regression analyses were performed to identify risk factors for endocrine abnormalities and the effect of endocrine abnormalities on OS, adjusting for confounders including the number and duration of ICI administrations.

Results: Single and multiple endocrine abnormalities were observed in 12.0% and 1.4% of patients, respectively. The most common combination was hypothyroidism and adrenal insufficiency (1.3%). Kaplan-Meier analysis indicated better survival in patients with multiple and single endocrine abnormalities than in those without (P < .01). Multivariable analysis revealed lower mortality in patients with multiple and single endocrine abnormalities (adjusted hazard ratio [aHR] 0.39; 95% confidence interval [CI], 0.28-0.54, P < .01; aHR 0.65; 95% CI, 0.5-80.72, P < .01, respectively) than in those without. Mortality was significantly lower with multiple abnormalities than with single (aHR 0.56; 95% CI, 0.39-0.79, P < .01).

Conclusions: The development of multiple endocrine abnormalities in patients treated with ICIs is associated with improved survival compared with that of patients with a single abnormality.

与免疫检查点抑制剂相关的多重或单一内分泌异常。
背景:免疫检查点抑制剂(ICIs)与多种内分泌异常有关。然而,其潜在的病理生理机制尚不清楚。我们研究了多种内分泌异常对ICIs患者总生存期(OS)的影响。方法:使用DeSC日本行政索赔数据库,对2014年至2022年期间接受ICIs的12,978例患者进行调查。内分泌异常由各种激素替代疗法定义,包括左甲状腺素、氢化可的松和胰岛素,其中难以区分中枢或原发性激素缺陷。此外,仅包括甲状腺炎后甲状腺功能减退的患者。1型糖尿病还被定义为疾病的名称和严格的自我注射费用。进行回归分析以确定内分泌异常的危险因素和内分泌异常对OS的影响,调整混杂因素,包括ICI给药次数和持续时间。结果:单发内分泌异常占12.0%,多发内分泌异常占1.4%。最常见的合并是甲状腺功能减退和肾上腺功能不全(1.3%)。Kaplan-Meier分析显示,多发或单发内分泌异常患者的生存率高于无内分泌异常患者(P < 0.01)。多变量分析显示,多重和单一内分泌异常患者的死亡率较低(校正风险比[aHR] 0.39;95%置信区间[CI], 0.28-0.54, P < 0.01;aHR 0.65;95% CI, 0.5 ~ 80.72, P < 0.01)。多重异常的死亡率明显低于单一异常(aHR 0.56;95% ci, 0.39-0.79, p < 0.01)。结论:与单一内分泌异常患者相比,接受ICIs治疗的患者发生多发性内分泌异常可提高生存率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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