Protein Kinase Inhibitors Indicated for Lung Cancer: Pharmacodynamics, Pharmacokinetics, Adverse Drug Reactions, and Evaluation in Clinical Trials

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Constance Bordet, Vincent Dongay, Yoann Zelmat, Julien Mazieres, Fabien Despas
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引用次数: 0

Abstract

WhatIs Known and Objective. Anti-EGFR (epidermal growth factor receptor) drugs are indicated for non-small-cell lung cancer (NSCLC). This review summarises the information available to date on the first anti-EGFRs granted market authorisation: erlotinib TARCEVA®, gefitinib IRESSA®, afatinib GIOTRIF®, dacomitinib VIZIMPRO®, and osimertinib TAGRISSO®. Methods. A literature search was conducted in the PubMed database including studies published in English using the terms gefitinib, erlotinib, afatinib, dacomitinib, and osimertinib. Furthermore, bibliographies of selected references were also studied for relevant articles. Clinical trial (CT) data were extracted from clinicaltrials.gov (ongoing trials and adverse events (AEs)). Assessment of AEs for these drugs was conducted using global pharmacovigilance data from VigiBase®. Results and Discussion. Erlotinib and gefitinib are first-generation anti-EGFR drugs, able to bind competitively and reversibly to the ATP- (adenosine triphosphate-) binding site of the EGFR exon 19 and exon 21 mutations. Afatinib and dacomitinib are second-generation anti-EGFRs able to bind covalently and irreversibly to the ATP site and inhibit EGFR and HER (human epidermal growth factor receptor) such as HER2 and HER4 enzyme activity. Osimertinib is a third-generation PKI and overcomes the EGFR T790M gatekeeper mutation through covalent binding at the ATP site. Medical interactions with these drugs are reported, notably with cytochrome P450 inducers or inhibitors. The most reported AEs in CTs are cutaneous reactions and gastrointestinal disorders. The occurrence of cutaneous reactions is less reported with third generation than with first- and second-generation anti-EGFR drugs. These results are consistent with the results from the VigiBase® global pharmacovigilance database. What Is New and Conclusion. This review summarises current knowledge regarding five anti-EGFRs in the literature. The third-generation anti-EGFR appears to be more effective than the first and second generations and is indicated as first-line therapy. This trial is registered with NCT01523587, NCT01466660, NCT01774721, NCT01360554, and NCT02296125.

Abstract Image

适用于肺癌的蛋白激酶抑制剂:药效学、药代动力学、药物不良反应和临床试验评估
已知信息和目标。抗表皮生长因子受体(EGFR)药物适用于非小细胞肺癌(NSCLC)。本综述总结了迄今为止获得市场授权的首批抗表皮生长因子受体药物的相关信息:厄洛替尼 TARCEVA®、吉非替尼 IRESSA®、阿法替尼 GIOTRIF®、达科米替尼 VIZIMPRO® 和奥西美替尼 TAGRISSO®。研究方法在PubMed数据库中使用吉非替尼、厄洛替尼、阿法替尼、达科米替尼和奥希替尼等词条进行文献检索,包括用英语发表的研究。此外,还研究了部分参考文献的书目,以查找相关文章。临床试验(CT)数据摘自 clinicaltrials.gov(正在进行的试验和不良事件(AEs))。使用 VigiBase® 中的全球药物警戒数据对这些药物的 AEs 进行了评估。结果与讨论厄洛替尼和吉非替尼是第一代抗表皮生长因子受体药物,能与表皮生长因子受体19号外显子和21号外显子突变的ATP(三磷酸腺苷)结合位点发生竞争性和可逆性结合。阿法替尼(Afatinib)和达科米替尼(dacomitinib)是第二代抗表皮生长因子受体药物,能够与 ATP 位点共价和不可逆地结合,抑制表皮生长因子受体和 HER(人表皮生长因子受体),如 HER2 和 HER4 的酶活性。奥希替尼是第三代 PKI,通过与 ATP 位点共价结合克服表皮生长因子受体 T790M 守门员突变。据报道,这些药物会发生医学相互作用,特别是与细胞色素 P450 诱导剂或抑制剂的相互作用。CT 中报告最多的 AE 是皮肤反应和胃肠功能紊乱。与第一代和第二代抗表皮生长因子受体(EGFR)药物相比,第三代药物发生皮肤反应的报道较少。这些结果与 VigiBase® 全球药物警戒数据库的结果一致。新内容与结论。本综述总结了目前文献中有关五种抗EGFR 药物的知识。第三代抗EGFR似乎比第一代和第二代更有效,可作为一线疗法。该试验已在 NCT01523587、NCT01466660、NCT01774721、NCT01360554 和 NCT02296125 上注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
226
审稿时长
6 months
期刊介绍: The Journal of Clinical Pharmacy and Therapeutics provides a forum for clinicians, pharmacists and pharmacologists to explore and report on issues of common interest. Reports and commentaries on current issues in medical and pharmaceutical practice are encouraged. Papers on evidence-based clinical practice and multidisciplinary collaborative work are particularly welcome. Regular sections in the journal include: editorials, commentaries, reviews (including systematic overviews and meta-analyses), original research and reports, and book reviews. Its scope embraces all aspects of clinical drug development and therapeutics, including: Rational therapeutics Evidence-based practice Safety, cost-effectiveness and clinical efficacy of drugs Drug interactions Clinical impact of drug formulations Pharmacogenetics Personalised, stratified and translational medicine Clinical pharmacokinetics.
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