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揭示癌症患者抗血管生成药物安全性概况中的知识空白:来自自发报告系统研究的见解

Uncovering Knowledge Gaps in the Safety Profile of Antiangiogenic Drugs in Cancer Patients: Insights from Spontaneous Reporting Systems Studies.

作者信息

Ciccone Valerio, Ziche Marina, Spini Andrea, Donnini Sandra

机构信息

Department of Life Sciences, University of Siena, Via Aldo Moro 2, 53100 Siena, Italy.

Department of Medicine Surgery and Neuroscience, University of Siena, Viale Mario Bracci 16, 53100 Siena, Italy.

出版信息

Pharmaceuticals (Basel). 2023 Jun 12;16(6):867. doi: 10.3390/ph16060867.

Abstract

Global repositories of postmarketing safety reports improve understanding of real-life drug toxicities, often not observed in clinical trials. The aim of this scoping review was to map the evidence from spontaneous reporting systems studies (SRSs) of antiangiogenic drugs (AADs) in cancer patients and highlight if the found disproportionality signals of adverse events (AEs) were validated and thus mentioned in the respective Summary of product Characteristics (SmPC). This scoping review was conducted according to PRISMA guidelines for scoping reviews. A knowledge gap on the safety of AADs was found: firstly, several cardiovascular AEs were not mentioned in the SmPCs and no pharmacovigilance studies were conducted despite the well-known safety concerns about these drugs on the cardiovascular system. Second, a disproportionality signal (not validated through causality assessment) of pericardial disease was found in the literature for axitinib with no mention in SmPC of the drug. Despite the exclusion of pharmacoepidemiological studies, we believe that this scoping review, which focuses on an entire class of drugs, could be considered as a novel approach to highlight possible safety concerns of drugs and as a guide for the conduction of a target postmarketing surveillance on AADs.

摘要

上市后安全性报告的全球数据库有助于增进对现实生活中药物毒性的了解,而这些毒性在临床试验中往往未被观察到。本范围综述的目的是梳理癌症患者抗血管生成药物(AAD)的自发报告系统研究(SRS)中的证据,并强调所发现的不良事件(AE)不成比例信号是否得到验证,以及是否在相应的产品特性摘要(SmPC)中提及。本范围综述是根据PRISMA范围综述指南进行的。发现了AAD安全性方面的知识空白:首先,SmPC中未提及几种心血管AE,尽管对这些药物在心血管系统方面的安全性担忧众所周知,但未开展药物警戒研究。其次,文献中发现阿昔替尼存在心包疾病的不成比例信号(未通过因果关系评估验证),而该药物的SmPC中未提及。尽管排除了药物流行病学研究,但我们认为,本范围综述聚焦于一整类药物,可被视为突出药物可能存在的安全问题的一种新方法,以及对AAD进行针对性上市后监测的指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eff1/10302288/b309871813c6/pharmaceuticals-16-00867-g001.jpg

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