Kohno Hiroki, Yanai Masaaki, Nishigami Miyu, Moriyama Shiro, Inui Genki, Nonaka Takafumi, Hoshino Yoshiki, Funaki Yoshihiro, Nagahara Takakazu, Kodani Masahiro, Yamasaki Akira
Division of Respiratory Medicine and Rheumatology, Department of Multidisciplinary Internal Medicine, Faculty of Medicine, Tottori University, Yonago, Japan.
Cancer Center, Tottori University Hospital, Yonago, Japan.
Int J Clin Oncol. 2025 Aug 21. doi: 10.1007/s10147-025-02862-7.
Immune checkpoint inhibitors (ICIs) improve cancer survival but can induce immune-related adverse events (irAEs). Pre-existing autoantibodies, particularly antinuclear antibodies (ANAs), have been suggested as predictive biomarkers for irAE development. However, prior studies have yielded mixed results. Furthermore, the predictive value of specific ANA staining patterns has remained unexplored. We aimed to investigate the relationship between baseline autoantibody levels and irAE development.
This retrospective observational study included 626 patients with cancer receiving ICI therapy between November 2020 and August 2024 at the Tottori University Hospital. irAEs were graded using Common Terminology Criteria for Adverse Events v5.0, with grade ≥ 2 considered clinically significant. Logistic regression analysis assessed the association between baseline factors and irAE development. Receiver operating characteristic (ROC) curve analysis evaluated model performance.
Elevated ANA titers (≥ ×40), speckled ANA staining pattern, and combination ICI therapy were significantly associated with an increased risk of grade ≥ 2 irAEs in both univariable and multivariable analyses. The predictive performance of the area under the ROC curve for the multivariable models using either elevated ANA titers or the speckled pattern was similar (approximately 0.617).
Baseline ANA titer and speckled ANA pattern are potential predictive biomarkers for grade ≥ 2 irAEs, particularly in patients receiving combination ICI therapy. Comprehensive ANA testing may improve risk stratification and inform personalized irAE management.
免疫检查点抑制剂(ICIs)可提高癌症患者的生存率,但会诱发免疫相关不良事件(irAEs)。先前存在的自身抗体,尤其是抗核抗体(ANAs),被认为是irAE发生的预测生物标志物。然而,既往研究结果不一。此外,特定ANA染色模式的预测价值仍未得到探索。我们旨在研究基线自身抗体水平与irAE发生之间的关系。
这项回顾性观察性研究纳入了2020年11月至2024年8月在鸟取大学医院接受ICI治疗的626例癌症患者。使用不良事件通用术语标准v5.0对irAEs进行分级,≥2级被认为具有临床意义。逻辑回归分析评估基线因素与irAE发生之间的关联。受试者工作特征(ROC)曲线分析评估模型性能。
在单变量和多变量分析中,ANA滴度升高(≥×40)、斑点状ANA染色模式和联合ICI治疗均与≥2级irAEs风险增加显著相关。使用升高的ANA滴度或斑点状模式的多变量模型的ROC曲线下面积的预测性能相似(约为0.617)。
基线ANA滴度和斑点状ANA模式是≥2级irAEs的潜在预测生物标志物,尤其是在接受联合ICI治疗的患者中。全面的ANA检测可能会改善风险分层并为个性化的irAE管理提供依据。