Lin Yuhao, Deng Muling, Xu Siqi, Chen Chuanben, Ding Jianming
Department of Radiation Oncology, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.
Oncology. 2025 Jan 24:1-9. doi: 10.1159/000542989.
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.
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.
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.
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.
替莫唑胺(TMZ)是一种广泛用于治疗恶性胶质瘤和其他脑肿瘤的化疗药物。尽管其已证实具有治疗益处,但仍需要更好地了解其安全性,特别是在真实世界的临床环境中。本研究旨在通过利用美国食品药品监督管理局不良事件报告系统(FAERS)数据库来识别与TMZ相关的严重药物不良反应(ADR),从而为临床实践提供有价值的安全性见解。
我们使用报告比值比、比例报告比、贝叶斯置信传播神经网络和经验贝叶斯几何均值作为不成比例分析的主要算法。仅在满足所有四种算法设定的标准时,不良事件(AE)才被分类为ADR。为确保结果的准确性,我们精心排除了任何被认为与TMZ无关的AE。
从2003年10月到2023年9月,从FAERS数据库中检索到总共10,502,538例病例报告,其中9,073例明确归因于TMZ。应用我们的筛选标准后,在18个系统器官类别(SOC)中识别出116种ADR,每种ADR都有相应的首选术语(PT)。识别出的与TMZ相关的ADR主要涉及骨髓抑制、肝毒性和各种感染,特别是耶氏肺孢子菌肺炎。此外,我们的分析还识别出药物标签中未列出的有价值的ADR,包括SOC层面的先天性、家族性和遗传性疾病,以及PT层面的意外ADR,如癫痫发作、肺栓塞和败血症。
这项真实世界的药物警戒研究已经识别出与TMZ相关的重大且先前未报告的ADR。迫切需要进一步的研究进行验证和解决,以指导TMZ的临床应用,确保其在治疗脑肿瘤中的使用安全有效。