Post-Marketing Safety of Temozolomide: A Pharmacovigilance Study Based on the Food and Drug Administration Adverse Event Reporting System.

IF 1.8 3区 医学 Q3 ONCOLOGY Oncology Pub Date : 2025-01-01 Epub Date: 2025-01-24 DOI:10.1159/000542989
Yuhao Lin, Muling Deng, Siqi Xu, Chuanben Chen, Jianming Ding, Jianming Ding
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Abstract

Introduction: Temozolomide (TMZ) is a widely used chemotherapy agent for the treatment of malignant gliomas and other brain tumors. Despite its established therapeutic benefits, there is an ongoing need to understand better its safety profile, particularly in real-world clinical settings. This study aimed to identify critical adverse drug reactions (ADRs) associated with TMZ by utilizing the FDA Adverse Event Reporting System (FAERS) database, thereby providing valuable safety insights for clinical practice.

Methods: We utilized the reported odds ratio, proportional reporting ratio, Bayesian Confidence Propagation Neural Network, and Empirical Bayes Geometric Mean as primary algorithms for disproportionality analysis. Adverse events (AEs) were classified as ADRs only upon meeting the criteria set by all four algorithms. To ensure the accuracy of our results, we meticulously excluded any AEs deemed unrelated to TMZ.

Results: From October 2003 to September 2023, a total of 10,502,538 case reports and 9,073 cases explicitly attributed to TMZ were retrieved from the FAERS database. After applying our filters, 116 ADRs, each with a corresponding Preferred Term (PT), were identified across 18 System Organ Classes (SOCs). The identified ADRs associated with TMZ primarily involved bone marrow suppression, hepatotoxicity, and various infections, notably Pneumocystis jirovecii pneumonia. Furthermore, our analysis identified valuable ADRs not listed in the drug label, including congenital, familial, and genetic disorders at the SOC level, as well as unexpected ADRs at the PT level, such as seizures, pulmonary embolism, and sepsis.

Conclusion: This real-world pharmacovigilance study has identified significant and previously unreported ADRs associated with TMZ. Further research for validation and resolution is urgently needed to guide the clinical application of TMZ, ensuring the safety and efficacy of its use in treating brain tumors.

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替莫唑胺的上市后安全性:基于美国食品药品监督管理局不良事件报告系统的药物警戒研究。
替莫唑胺(Temozolomide, TMZ)是一种广泛应用于恶性胶质瘤等脑肿瘤的化疗药物。尽管已确定其治疗益处,但仍需要更好地了解其安全性,特别是在现实世界的临床环境中。本研究旨在利用FDA不良事件报告系统(FAERS)数据库识别与TMZ相关的关键药物不良反应(adr),从而为临床实践提供有价值的安全性见解。方法:我们使用报告的优势比、比例报告比、贝叶斯置信传播神经网络和经验贝叶斯几何平均作为歧化分析的主要算法。不良事件(ae)只有在满足所有四种算法设定的标准时才被归类为adr。为了确保结果的准确性,我们精心排除了任何与TMZ无关的ae。结果:2003年10月至2023年9月,FAERS数据库共检索到10502538例病例报告和9073例明确归属于TMZ的病例。在应用我们的过滤器后,在18个系统器官类别(soc)中确定了116个adr,每个adr都有相应的首选术语(PT)。已确定的与TMZ相关的不良反应主要包括骨髓抑制、肝毒性和各种感染,特别是肺囊虫肺炎。此外,我们的分析确定了药物标签中未列出的有价值的不良反应,包括SOC水平的先天性、家族性和遗传性疾病,以及PT水平的意外不良反应,如癫痫发作、肺栓塞和败血症。结论:这项现实世界的药物警戒研究已经确定了与TMZ相关的重大且以前未报道的不良反应。为了指导TMZ的临床应用,确保其治疗脑肿瘤的安全性和有效性,迫切需要进一步的研究进行验证和解决。
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来源期刊
Oncology
Oncology 医学-肿瘤学
CiteScore
6.00
自引率
2.90%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.
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