Nanki Toshihiro, Yamaguchi Tomohiro, Umetsu Kosei, Tanabe Ryunosuke, Maeda Naoki, Kanazawa Minori, Furuno Yuko, Matsuda Shinichi, Takemoto Shinya, Asao Keiko, Kamiuchi Tatsuya
Division of Rheumatology, Department of Internal Medicine, Toho University School of Medicine, Tokyo, Japan.
Drug Safety Division, Chugai Pharmaceutical Co. Ltd, Tokyo, Japan.
Clin Rheumatol. 2025 Mar;44(3):1081-1093. doi: 10.1007/s10067-025-07328-9. Epub 2025 Feb 7.
To develop a prediction model for serious infections (SIs) in rheumatoid arthritis (RA) patients treated with tocilizumab in Japan and to evaluate the model's performance compared to previously developed models, i.e., 'DANBIO' and 'postmarketing surveillance' (PMS).
This non-interventional retrospective cohort study utilized the Medical Data Vision database in Japan. The study population was derived from patients ≥ 18 years with RA who initiated tocilizumab between April 2008 and July 2021. SIs were assessed during the 1-year follow-up from tocilizumab initiation. The candidate predictors were identified based on previous studies, known risk factors, potentially relevant factors, and data availability. The prediction model was developed using logistic regression. The model's performance was compared with previously developed models using cross-entropy and area under the receiver operating characteristic curve (AUC).
Of the 6501 RA patients, 4.57% experienced SIs during the 1-year follow-up. The model included 17 predictors for SI (e.g., age (odds ratio 1.013 (95% confidence interval 1.002-1.024)), history of SIs (2.569 (1.636-3.745)), diverticulitis (2.183 (1.000-3.989))). The model showed a lower cross-entropy and a higher AUC (0.1488; 0.712) compared to DANBIO (0.1932; 0.591) and PMS (0.1561; 0.565) models, and the sensitivity, specificity, positive predictive value, and negative predictive value using 5% threshold were 72%, 64%, 7%, and 98%, respectively.
The model developed in this study seems to have the potential to inform the risk of SIs in RA patients treated with tocilizumab and may help the early identification of patients at risk of SIs to reduce morbidity and mortality.
建立日本接受托珠单抗治疗的类风湿关节炎(RA)患者严重感染(SI)的预测模型,并与先前开发的模型(即“DANBIO”和“上市后监测”(PMS))比较评估该模型的性能。
这项非干预性回顾性队列研究利用了日本的医学数据视觉数据库。研究人群来自2008年4月至2021年7月间开始使用托珠单抗的≥18岁RA患者。在开始使用托珠单抗后的1年随访期间评估SI。根据先前的研究、已知风险因素、潜在相关因素和数据可用性确定候选预测因素。使用逻辑回归建立预测模型。使用交叉熵和受试者工作特征曲线下面积(AUC)将该模型的性能与先前开发的模型进行比较。
在6501例RA患者中,4.57%在1年随访期间发生了SI。该模型包括17个SI预测因素(例如,年龄(比值比1.013(95%置信区间1.002 - 1.024))、SI病史(2.569(1.636 - 3.745))、憩室炎(2.183(1.000 - 3.989)))。与DANBIO模型(0.1932;0.591)和PMS模型(0.1561;r0.565)相比,该模型显示出更低的交叉熵和更高的AUC(0.1488;0.712),使用5%阈值时的灵敏度、特异度、阳性预测值和阴性预测值分别为72%、64%、7%和98%。
本研究中开发的模型似乎有潜力告知接受托珠单抗治疗的RA患者发生SI的风险,并可能有助于早期识别有SI风险的患者以降低发病率和死亡率。