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酪氨酸激酶抑制剂的心血管安全性:特别关注心脏复极(QT 间期)。

Cardiovascular safety of tyrosine kinase inhibitors: with a special focus on cardiac repolarisation (QT interval).

机构信息

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

出版信息

Drug Saf. 2013 May;36(5):295-316. doi: 10.1007/s40264-013-0047-5.

Abstract

The development of tyrosine kinase inhibitors (TKI) represents a major milestone in oncology. However, their use has been found to be associated with serious toxicities that impinge on various vital organs including the heart. Sixteen TKIs have been approved for use in oncology as of 30 September 2012, and a large number of others are in development or under regulatory review. Cardiovascular safety of medicinal products is a major public health issue that has concerned all the stakeholders. This review focuses on three specific cardiovascular safety aspects of TKIs, namely their propensity to induce QT interval prolongation, left ventricular (LV) dysfunction and hypertension (both systemic and pulmonary). Analyses of information in drug labels, the data submitted to the regulatory authorities and the published literature show that a number of TKIs are associated with these undesirable effects. Whereas LV dysfunction and systemic hypertension are on-target effects related to the inhibition of ligand-related signalling pathways, QT interval prolongation appears to be an off-target class III electrophysiologic effect, possibly related to the presence of a fluorine-based pharmacophore. If not adequately managed, these cardiovascular effects significantly increase the morbidity and mortality in a population already at high risk. Hitherto, the QT effect of most QT-prolonging TKIs (except lapatinib, nilotinib, sunitinib and vandetanib) is relatively mild at clinical doses and has not led to appreciable morbidity clinically. In contrast, LV dysfunction and untreated hypertension have resulted in significant morbidity. Inevitably, dilemmas arise in determining the risk/benefit of a TKI therapy in an individual patient who develops any of these effects following the treatment of the TKI-sensitive cancer. QT interval prolongation, hypertension and LV dysfunction can be managed effectively by using reliable methods of measurement and careful monitoring of patients whose clinical management requires optimisation by a close collaboration between an oncologist and a cardiologist, an evolving subspecialty referred to as cardio-oncology. Despite their potential adverse clinical impact, the effects of TKIs on hypertension and LV function are generally inadequately characterised during their development. As has been the case with QT liability of drugs, there is now a persuasive case for a regulatory requirement to study TKIs systematically for these effects. Furthermore, since most of these novel drugs are studied in trials with relatively small sample sizes and approved on an expedited basis, there is also a compelling case for their effective pharmacovigilance and on-going reassessment of their risk/benefit after approval.

摘要

酪氨酸激酶抑制剂(TKI)的发展是肿瘤学的一个重要里程碑。然而,已经发现它们的使用与严重的毒性有关,这些毒性会影响包括心脏在内的各种重要器官。截至 2012 年 9 月 30 日,已有 16 种 TKI 被批准用于肿瘤学,还有大量其他药物正在开发或正在监管审查中。药物的心血管安全性是一个主要的公共卫生问题,引起了所有利益相关者的关注。本综述重点关注 TKI 的三个特定心血管安全性方面,即它们诱导 QT 间期延长、左心室(LV)功能障碍和高血压(包括系统性和肺动脉高压)的倾向。对药物标签中的信息、向监管机构提交的数据和已发表文献的分析表明,一些 TKI 与这些不良影响有关。虽然 LV 功能障碍和系统性高血压是与配体相关信号通路抑制相关的靶标效应,但 QT 间期延长似乎是一种非靶标 III 类电生理效应,可能与氟基药效团的存在有关。如果得不到充分管理,这些心血管效应会显著增加已经处于高风险的人群的发病率和死亡率。迄今为止,大多数延长 QT 间期的 TKI(拉帕替尼、尼罗替尼、舒尼替尼和凡德他尼除外)的 QT 效应在临床剂量下相对较轻,并且在临床上没有导致明显的发病率。相比之下,LV 功能障碍和未经治疗的高血压导致了显著的发病率。不可避免的是,在确定接受 TKI 敏感癌症治疗后出现这些效应的个体患者的 TKI 治疗的风险/获益时,会出现两难境地。QT 间期延长、高血压和 LV 功能障碍可以通过使用可靠的测量方法和仔细监测来有效管理,临床管理需要肿瘤学家和心脏病学家之间的密切合作来优化,这是一个不断发展的亚专业,称为心脏肿瘤学。尽管 TKI 对高血压和 LV 功能的影响具有潜在的临床不良影响,但在其开发过程中通常对这些影响的描述不足。就像药物的 QT 倾向一样,现在有一个有说服力的案例需要监管要求系统地研究 TKI 的这些影响。此外,由于大多数这些新型药物都是在相对较小的样本量的试验中进行研究,并在加速的基础上获得批准,因此也有一个强有力的案例需要对它们进行有效的药物警戒,并在批准后对其风险/获益进行持续重新评估。

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