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Drug interactions with solid tumour-targeted therapies

机译:药物与实体瘤靶向疗法的相互作用

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Drug interactions are an on-going concern in the treatment of cancer, especially when targeted therapies, such as tyrosine kinase inhibitors (TKI) or mammalian target of rapamycin (mTOR) inhibitors, are being used. The emergence of elderly patients and/or patients with both cancer and other chronic co-morbidities leads to polypharmacy. Therefore, the risk of drug-drug interactions (DDI) becomes a clinically relevant issue, all the more so as TKIs and mTOR inhibitors are essentially metabolised by cytochrome P450 enzymes. These DDIs can result in variability in anticancer drug exposure, thus favouring the selection of resistant cellular clones or the occurrence of toxicity. This review provides a comprehensive overview of DDIs that involve targeted therapies approved by the FDA for the treatment of solid tumours for more than 3 years (sorafenib, sunitinib, erlotinib, gefitinib, imatinib, lapatinib, everolimus, temsirolimus) and medicinal herb or drugs. This review also provides some guidelines to help oncologists and pharmacists in their clinical practice.
机译:在癌症的治疗中,药物相互作用一直是一个持续关注的问题,尤其是当使用靶向治疗,例如酪氨酸激酶抑制剂(TKI)或雷帕霉素哺乳动物靶标(mTOR)抑制剂时。老年患者和/或患有癌症和其他慢性合并症的患者的出现导致了多药治疗。因此,药物-药物相互作用(DDI)的风险已成为临床相关问题,因为TKI和mTOR抑制剂基本上被细胞色素P450酶代谢。这些DDI可以导致抗癌药物暴露的差异,从而有利于选择抗性细胞克隆或发生毒性反应。这篇综述提供了DDI的全面概述,这些DDI涉及FDA批准的用于治疗实体瘤超过3年的靶向疗法(索拉非尼,舒尼替尼,厄洛替尼,吉非替尼,伊马替尼,拉帕替尼,依维莫司,替西罗莫司)和药用草药或药物。这篇综述还提供了一些指南,以帮助肿瘤科医生和药剂师进行临床实践。

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