药物性肿瘤疾病:全球药物警戒数据库分析。

IF 2.2 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Yoann Zelmat, Fabien Despas
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引用次数: 0

摘要

导言:癌症仍然是一个全球性的威胁,在2020年造成近1000万人死亡。美国癌症协会已经确定了已知的和可能的致癌物,包括常用的药物。本研究的目的是描述在癌症发生中最常报道的药物。方法:在全球药物警戒数据库VigiBase的所有个案安全报告(ICSRs)中,我们检索了截至2023年6月30日的50种报告最多的药物,这些药物的不良反应术语属于“恶性或未指定肿瘤”的查询。然后,我们提取歧化测量数据、信息成分(IC)和报告优势比(ROR),以评估歧化信号。结果:在VigiBase的所有icsr中,871,925例包含属于SMQ“恶性或未明确肿瘤”的不良反应。雷尼替丁是报告癌症相关不良反应最多的药物(n=106,484),其次是来那度胺(n=13,466)和依那西普(n=8014)。IC最高的药物为雷尼替丁(IC=5.2, 95%可信区间[95% CI]=5.2 ~ 5.2)、吡格列酮(1353个ICSRs, IC=4.2, 95% CI=4.2 ~ 4.2)和瑞非尼(1272个ICSRs, IC=2.8, 95% CI=2.8 ~ 2.8)。讨论:我们的研究结果表明,主要的药理学机制与雷尼替丁(与雷尼替丁类药物中n -亚硝基二甲胺的水平有关)、基因激活药物(吡格列酮:各种具有免疫抑制作用的药理学家族(蛋白激酶抑制剂、免疫调节剂、硫唑嘌呤等),某些类型的蛋白激酶抑制剂(其致癌机制尚不清楚)(瑞非尼、索拉非尼、伊马替尼、依鲁替尼等),以及激素拮抗剂(他莫昔芬、来曲唑)。可能需要对接触这些药物的患者进行特殊监测。需要进一步的研究来评估该排名中某些药物的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug-induced tumoral disease: A global pharmacovigilance database analysis

Introduction

Cancer remains a worldwide threat, having caused almost 10 million deaths in 2020. The American Cancer Society has identified both known and probable carcinogens, including commonly used drugs. The aim of this study is to describe the drugs most frequently reported in the occurrence of cancer.

Methods

Among all individual case safety reports (ICSRs) in the global pharmacovigilance database VigiBase, we searched for the 50 most reported drugs with an adverse drug reaction term belonging to the query “Malignant or unspecified tumors” until June 30, 2023. Then, we extracted the disproportionality measurement data, information component (IC), and reporting odds ratio (ROR) in order to assess a disproportionality signal.

Results

Among all ICSRs in VigiBase, 871,925 contained an ADR belonging to the SMQ “Malignant or unspecified tumors”. Ranitidine was the drug with the most reported ADRs related to cancer (n = 106,484), followed by lenalidomide (n = 13,466), and etanercept (n = 8014). The drugs with the highest IC were ranitidine (IC = 5.2, 95% confidence interval [95% CI] = 5.2–5.2), pioglitazone (1353 ICSRs, IC = 4.2, 95% CI = 4.2–4.2), and regorafenib (1272 ICSRs, IC = 2.8, 95% CI = 2.8–2.8).

Discussion

Our results show that the main pharmacological mechanisms are associated with ranitidine (link with levels of N-nitrosodimethylamine in ranitidine-based drugs), gene-activating drugs (pioglitazone: link with agonist effects on PPAR-γ gene activation), various pharmacological families with immunosuppressive effects (protein kinase inhibitors, immunomodulators, azathioprine, etc.), certain types of protein kinase inhibitors whose oncogenic mechanisms remain unclear (regorafenib, sorafenib, imatinib, ibrutinib, etc.), and hormone antagonists (tamoxifen, letrozole). Special monitoring of patients exposed to these drugs may be required. Further studies are needed to assess the risk with certain drugs in this ranking.

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来源期刊
Therapie
Therapie 医学-药学
CiteScore
3.50
自引率
7.70%
发文量
132
审稿时长
57 days
期刊介绍: Thérapie is a peer-reviewed journal devoted to Clinical Pharmacology, Therapeutics, Pharmacokinetics, Pharmacovigilance, Addictovigilance, Social Pharmacology, Pharmacoepidemiology, Pharmacoeconomics and Evidence-Based-Medicine. Thérapie publishes in French or in English original articles, general reviews, letters to the editor reporting original findings, correspondence relating to articles or letters published in the Journal, short articles, editorials on up-to-date topics, Pharmacovigilance or Addictovigilance reports that follow the French "guidelines" concerning good practice in pharmacovigilance publications. The journal also publishes thematic issues on topical subject. The journal is indexed in the main international data bases and notably in: Biosis Previews/Biological Abstracts, Embase/Excerpta Medica, Medline/Index Medicus, Science Citation Index.
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