Analysis of the risk of oncological adverse events associated with infliximab in combination with azathioprine compared to monotherapy: insights from the FAERS database.

IF 4.8 2区 医学 Q1 PHARMACOLOGY & PHARMACY Frontiers in Pharmacology Pub Date : 2025-01-08 eCollection Date: 2024-01-01 DOI:10.3389/fphar.2024.1507196
Qian Qiao, Jiachen Sun, Ya Zheng, Yingying Mi, Yanan Gong, Jiahui Liu, Wenyue Rui, Yumei Ma, Yongning Zhou, Min Liu
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Abstract

Objective: This study aimed to evaluate the risk of tumor formation with infliximab or azathioprine monotherapy versus their combination, using the FDA Adverse Event Reporting System (FAERS) database.

Methods: Data were extracted from the FAERS database for patients treated with infliximab, azathioprine, and combination therapy from Q1 2004 to Q2 2024. Signal mining employed methods such as Reported Odds Ratio (ROR), Proportional Reporting Ratio (PRR), Multiple Gamma-Poisson Scaling Assessment (MGPSA) and Bayesian Confidence Interval Progressive Neural Network (BCPNN).

Results: Our analysis of the FAERS database revealed that the highest number of reported cases involved skin-related tumors, both individually and in combination. In terms of sex, the risk of cancer was higher in men compared to women in the infliximab-only and combination groups; however, no sex difference was observed in the azathioprine-only group. Regarding age, we noted an increasing incidence of adverse tumor events in middle-aged and elderly individuals compared to minors, except in the azathioprine group, where age was not identified as an independent risk factor. Additionally, body weight was not found to be an independent risk factor in any of the three medication groups. After controlling for age, sex, and body weight, combination therapy did not increase the risk of tumor development compared to the azathioprine group alone. In contrast, for patients using infliximab alone, combination therapy not only did not elevate the risk of tumor development but also appeared to reduce it. The results of the Weber distribution suggest a random failure-type profile for the infliximab and azathioprine-only group, while an early failure-type profile was observed for the combination therapy. Furthermore, we analyzed the median time to onset and cumulative incidence rates, revealing no significant differences in median time to tumor onset or cumulative incidence rates between the combination therapy and the single agent.

Conclusion: After adjusting for age, sex, and body weight, combination therapy did not significantly increase tumor development risk compared to the azathioprine-only group. Additionally, in patients on infliximab monotherapy, combination therapy appeared to reduce the risk of tumor development.

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与单药治疗相比,英夫利昔单抗联合硫唑嘌呤的肿瘤不良事件风险分析:来自FAERS数据库的见解。
目的:本研究旨在利用FDA不良事件报告系统(FAERS)数据库,评估英夫利昔单抗或硫唑嘌呤单药治疗与联合治疗的肿瘤形成风险。方法:从FAERS数据库中提取2004年第一季度至2024年第二季度接受英夫利昔单抗、硫唑嘌呤和联合治疗的患者的数据。信号挖掘采用报告优势比(ROR)、比例报告比(PRR)、多重伽玛泊松尺度评估(MGPSA)和贝叶斯置信区间渐进神经网络(BCPNN)等方法。结果:我们对FAERS数据库的分析显示,报告的病例中涉及皮肤相关肿瘤的病例最多,无论是单独的还是联合的。在性别方面,在英夫利昔单抗单用组和联合组中,男性患癌症的风险高于女性;然而,在仅硫唑嘌呤组中没有观察到性别差异。关于年龄,我们注意到与未成年人相比,中老年个体的不良肿瘤事件发生率增加,除了硫唑嘌呤组,年龄未被确定为独立的危险因素。此外,在三组药物中,体重并不是一个独立的危险因素。在控制了年龄、性别和体重后,与单独使用硫唑嘌呤组相比,联合治疗没有增加肿瘤发展的风险。相比之下,对于单独使用英夫利昔单抗的患者,联合治疗不仅没有增加肿瘤发展的风险,而且似乎降低了肿瘤发展的风险。韦伯分布的结果表明,英夫利昔单抗和硫唑嘌呤组的失败类型是随机的,而联合治疗组的失败类型是早期的。此外,我们分析了中位发病时间和累积发病率,发现联合治疗和单药治疗在中位发病时间和累积发病率方面没有显著差异。结论:在调整了年龄、性别和体重后,与单硫唑嘌呤组相比,联合治疗并未显著增加肿瘤发展风险。此外,在接受英夫利昔单抗单药治疗的患者中,联合治疗似乎降低了肿瘤发展的风险。
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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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