Tyrosine Kinase Inhibitors and Interstitial Lung Disease: A Disproportionality Analysis Using the European Post-marketing EudraVigilance Database.

IF 1.9 Q3 PHARMACOLOGY & PHARMACY
Devron R Shah, Simon P Hart, Dominic L Sykes
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Abstract

Background: Increasing global frequency of drug-induced interstitial lung disease (ILD) coincides with increasing market introduction of tyrosine kinase inhibitors (TKIs).

Objectives: The aim was to detect disproportional reporting of TKI-induced ILD in the EudraVigilance post-marketing safety database and to scrutinise the prescribing information of these TKIs.

Methods: Data were gathered on the number of total and individual ILD case safety reports for each TKI marketed in the European Union (EU), together with indications and patient demographics. Information was also obtained on numbers of total and ILD reports for all drugs in the entire database, covering the period January 2002 to March 2024. Chi-squared analyses and two measures of disproportionality, the proportional reporting ratio (PRR) and reporting odds ratio (ROR), were used to ascertain the ILD-inducing potential of TKIs, both as a group and with each TKI individually. The latest prescribing information for each TKI was evaluated for ILD-related information.

Results: TKIs were collectively associated with a significantly stronger disproportionality signal for ILD reports compared to all non-TKI drugs (p < 0.001). There was marked variation in the disproportionality of ILD reporting across the 51 TKIs studied. Potential risk factors included male gender (p < 0.001), age 65-85 years (p < 0.001) and an oncological indication (p < 0.001), particularly non-small cell lung cancer (NSCLC). Fatality rates among cases of TKI-induced ILD were 17.4% overall, 22.2% in patients with NSCLC and 11.5% in those with a non-oncological indication. The prescribing information of 11 TKIs lacked any reference to ILD despite a strong signal that indicated their potential association with ILD.

Conclusions: Drug-induced ILD is emerging as an important safety issue, and physicians need to maintain a high index of suspicion of ILD in patients treated with a TKI.

酪氨酸激酶抑制剂和间质性肺疾病:使用欧洲上市后EudraVigilance数据库的歧化分析
背景:全球药物性间质性肺疾病(ILD)发病率的增加与酪氨酸激酶抑制剂(TKIs)市场引入的增加相一致。目的:目的是在eudravilance上市后安全性数据库中检测tki诱导ILD的不成比例报告,并仔细检查这些tki的处方信息。方法:收集在欧盟(EU)销售的每种TKI的总体和个体ILD病例安全报告数量,以及适应症和患者人口统计数据。还获得了整个数据库中所有药物的总数和ILD报告数量的信息,涵盖2002年1月至2024年3月。采用卡方分析和比例报告比(PRR)和报告优势比(ROR)两种不相称性测量来确定TKI作为一个群体和每个TKI单独诱导ild的潜力。评估每种TKI的最新处方信息,以获取ild相关信息。结果:与所有非tki药物相比,tki与ILD报告的歧化信号显著更强(p < 0.001)。在研究的51例tki中,ILD报告的不相称性存在显著差异。潜在的危险因素包括男性(p < 0.001)、65-85岁(p < 0.001)和肿瘤适应症(p < 0.001),特别是非小细胞肺癌(NSCLC)。tki诱导ILD的病死率为17.4%,非小细胞肺癌患者为22.2%,非肿瘤指征患者为11.5%。11例tki的处方信息缺乏任何与ILD相关的信息,尽管有强烈的信号表明它们可能与ILD相关。结论:药物性ILD正在成为一个重要的安全问题,医生需要对接受TKI治疗的患者保持高度的ILD怀疑指数。
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来源期刊
Drugs - Real World Outcomes
Drugs - Real World Outcomes PHARMACOLOGY & PHARMACY-
CiteScore
3.60
自引率
5.00%
发文量
49
审稿时长
8 weeks
期刊介绍: Drugs - Real World Outcomes targets original research and definitive reviews regarding the use of real-world data to evaluate health outcomes and inform healthcare decision-making on drugs, devices and other interventions in clinical practice. The journal includes, but is not limited to, the following research areas: Using registries/databases/health records and other non-selected observational datasets to investigate: drug use and treatment outcomes prescription patterns drug safety signals adherence to treatment guidelines benefit : risk profiles comparative effectiveness economic analyses including cost-of-illness Data-driven research methodologies, including the capture, curation, search, sharing, analysis and interpretation of ‘big data’ Techniques and approaches to optimise real-world modelling.
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