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酪氨酸激酶抑制剂的肝毒性:临床与监管视角。

Hepatotoxicity of tyrosine kinase inhibitors: clinical and regulatory perspectives.

机构信息

Rashmi Shah Consultancy Ltd, 8 Birchdale, Gerrards Cross, Buckinghamshire, SL9 7JA, UK.

出版信息

Drug Saf. 2013 Jul;36(7):491-503. doi: 10.1007/s40264-013-0048-4.

Abstract

The introduction of small-molecule tyrosine kinase inhibitors (TKIs) in clinical oncology has transformed the treatment of certain forms of cancers. As of 31 March 2013, 18 such agents have been approved by the US Food and Drug Administration (FDA), 15 of these also by the European Medicines Agency (EMA), and a large number of others are in development or under regulatory review. Unexpectedly, however, their use has been found to be associated with serious toxic effects on a number of vital organs including the liver. Drug-induced hepatotoxicity has resulted in withdrawal from the market of many widely used drugs and is a major public health issue that continues to concern all the stakeholders. This review focuses on hepatotoxic potential of TKIs. The majority of TKIs approved to date are reported to induce hepatic injury. Five of these (lapatinib, pazopanib, ponatinib, regorafenib and sunitinib) are sufficiently potent in this respect as to require a boxed label warning. Onset of TKI-induced hepatotoxicity is usually within the first 2 months of initiating treatment, but may be delayed, and is usually reversible. Fatality from TKI-induced hepatotoxicity is uncommon compared to hepatotoxic drugs in other classes but may lead to long-term consequences such as cirrhosis. Patients should be carefully monitored for TKI-induced hepatotoxicity, the management of which requires individually tailored reappraisal of the risk/benefit. The risk is usually manageable by dose adjustment or a switch to a suitable alternative TKI. Confirmation of TKI-induced hepatotoxicity can present challenges in the presence of hepatic metastasis and potential drug interactions. Its diagnosis in a patient with TKI-sensitive cancer requires great care if therapy with the TKI suspected to be causal is to be modified or interrupted as a result. Post-marketing experience with drugs such as imatinib, lapatinib and sorafenib suggests that the hepatotoxic safety of all the TKIs requires diligent surveillance.

摘要

小分子酪氨酸激酶抑制剂(TKI)在临床肿瘤学中的应用改变了某些类型癌症的治疗方法。截至 2013 年 3 月 31 日,美国食品和药物管理局(FDA)已批准了 18 种此类药物,其中 15 种也获得了欧洲药品管理局(EMA)的批准,还有大量其他药物正在开发或处于监管审查中。然而,出乎意料的是,它们的使用被发现与许多重要器官(包括肝脏)的严重毒性作用有关。药物性肝毒性导致许多广泛使用的药物被撤出市场,这是一个继续引起所有利益相关者关注的主要公共卫生问题。本综述重点介绍 TKI 的肝毒性潜力。迄今为止批准的大多数 TKI 据报道可引起肝损伤。其中 5 种(拉帕替尼、帕唑帕尼、波那替尼、瑞戈非尼和舒尼替尼)在这方面的效力足够强,需要使用黑框警告。TKI 诱导的肝毒性通常在开始治疗的前 2 个月内发生,但可能会延迟,并且通常是可逆的。与其他类别的肝毒性药物相比,TKI 诱导的肝毒性导致死亡的情况并不常见,但可能导致肝硬化等长期后果。应仔细监测患者的 TKI 诱导的肝毒性,其管理需要个体化评估风险/获益。通常可以通过调整剂量或改用合适的替代 TKI 来控制风险。在存在肝转移和潜在药物相互作用的情况下,确认 TKI 诱导的肝毒性可能会带来挑战。如果怀疑导致肝毒性的 TKI 药物需要修改或中断治疗,则在 TKI 敏感癌症患者中诊断 TKI 诱导的肝毒性需要格外小心。伊马替尼、拉帕替尼和索拉非尼等药物的上市后经验表明,所有 TKI 的肝毒性安全性都需要进行仔细监测。

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