Unveiling the Hidden Risks: An Update Decade-Long Analysis of Abraxane-Related Adverse Events from the FAERS Database.

IF 6.6 2区 医学 Q1 NANOSCIENCE & NANOTECHNOLOGY
International Journal of Nanomedicine Pub Date : 2024-11-14 eCollection Date: 2024-01-01 DOI:10.2147/IJN.S490400
Yue-Chen Zhao, Xin Li, Chao-Qun Wang, Yan Jiao, Yan-Nan Shen, Tie-Jun Wang, Chao-He Zhang
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Abstract

Purpose: Abraxane (nanoparticle albumin-bound paclitaxel) is a chemotherapeutic employed commonly for the management of various cancers including breast cancer, non-small cell lung cancer, and pancreatic adenocarcinoma. Although it has clinically beneficial properties, Abraxane is accompanied by multiple adverse events (AEs) that require close observation. This study aims to evaluate the AE profile of Abraxane using recently available data from January 2004 through December 2023 in the FDA Adverse Event Reporting System (FAERS).

Patients and methods: The data for Abraxane-related AEs were obtained from the FAERS database. The dataset consisted of patient demographic characteristics as well as information on the types and outcomes of AEs reported. Reporting odds ratios (ROR) as well as proportional reporting ratio (PRR), considering the used definition of anti-cancer agent and AEs, were calculated to investigate any association with Abraxane.

Results: A total of 10,310 reports associated with Abraxane AEs were identified. Blood and lymphatic system disorders were the most frequent (ROR 6.44), followed by hepatobiliary (ROR 3.16), infections (ROR 1.45), and gastrointestinal disorders (ROR 1.42). Serious outcomes included hospitalization in 36.35% and death in 29.76% of cases. The top adverse reactions matched known profiles, including peripheral sensory neuropathy (ROR: 49.48). The analysis also found new adverse reactions, such as scleroderma-like reactions (ROR: 95.4) and vascular pseudoaneurysm ruptures (ROR: 87.71).

Conclusion: Our results re-emphasize the importance of a robust Post Marketing Surveillance system and suggest this FAERS database based analysis provides an updated, independent information on Abraxane related AEs to enrich its safety profile. A process of continuous vigilance and additional investigations on specific areas that may have some undesired events are imperative to increase our knowledge on how Abraxane should be handled in terms of its safety.

揭开隐藏风险的面纱:对 FAERS 数据库中与 Abraxane 相关的不良事件的十年更新分析。
目的:Abraxane(纳米颗粒白蛋白结合型紫杉醇)是一种常用的化疗药物,用于治疗各种癌症,包括乳腺癌、非小细胞肺癌和胰腺癌。阿勃赛尼虽然具有临床疗效,但也伴随着多种不良反应(AE),需要密切观察。本研究旨在利用FDA不良事件报告系统(FAERS)中2004年1月至2023年12月的最新数据,评估Abraxane的AE概况:阿勃赛尼相关的AE数据来自FAERS数据库。数据集包括患者的人口统计学特征以及所报告的不良事件的类型和结果信息。考虑到所使用的抗癌药和AEs定义,计算了报告几率比(ROR)和报告比例比(PRR),以研究与阿勃赛尼的任何关联:结果:共发现10,310份与阿勃赛尼相关的AE报告。最常见的是血液和淋巴系统疾病(ROR 6.44),其次是肝胆疾病(ROR 3.16)、感染(ROR 1.45)和胃肠道疾病(ROR 1.42)。严重后果包括 36.35% 的病例住院,29.76% 的病例死亡。最主要的不良反应与已知情况相符,包括外周感觉神经病变(ROR:49.48)。分析还发现了新的不良反应,如硬皮病样反应(ROR:95.4)和血管假性动脉瘤破裂(ROR:87.71):我们的研究结果再次强调了健全的上市后监测系统的重要性,并表明基于FAERS数据库的分析提供了与Abraxane相关的AEs的最新独立信息,从而丰富了其安全性概况。为了增加我们对如何处理 Abraxane 安全性的了解,必须对可能发生不良事件的特定领域进行持续警惕和额外调查。
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来源期刊
International Journal of Nanomedicine
International Journal of Nanomedicine NANOSCIENCE & NANOTECHNOLOGY-PHARMACOLOGY & PHARMACY
CiteScore
14.40
自引率
3.80%
发文量
511
审稿时长
1.4 months
期刊介绍: The International Journal of Nanomedicine is a globally recognized journal that focuses on the applications of nanotechnology in the biomedical field. It is a peer-reviewed and open-access publication that covers diverse aspects of this rapidly evolving research area. With its strong emphasis on the clinical potential of nanoparticles in disease diagnostics, prevention, and treatment, the journal aims to showcase cutting-edge research and development in the field. Starting from now, the International Journal of Nanomedicine will not accept meta-analyses for publication.
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