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碘难治性分化型甲状腺癌的激酶抑制剂——聚焦于治疗相关高血压的发生、机制和管理。

Kinase-Inhibitors in Iodine-Refractory Differentiated Thyroid Cancer-Focus on Occurrence, Mechanisms, and Management of Treatment-Related Hypertension.

机构信息

Department of Biomedicine, Aarhus University, Ole Worms Allé 4, 8000 Aarhus, Denmark.

Division of Nuclear Medicine, Department of Radiology and Nuclear Medicine, Otto von Guericke University, Leipziger Str. 44, 39120 Magdeburg, Germany.

出版信息

Int J Mol Sci. 2021 Nov 12;22(22):12217. doi: 10.3390/ijms222212217.

Abstract

Differentiated thyroid cancer (DTC) usually has a good prognosis when treated conventionally with thyroidectomy, radioactive iodine (RAI) and thyroid-stimulating hormone suppression, but some tumors develop a resistance to RAI therapy, requiring alternative treatments. Sorafenib, lenvatinib and cabozantinib are multikinase inhibitors (MKIs) approved for the treatment of RAI-refractory DTC. The drugs have been shown to improve progression-free survival (PFS) and overall survival (OS) via the inhibition of different receptor tyrosine kinases (RTKs) that are involved in tumorigenesis and angiogenesis. Both sorafenib and lenvatinib have been approved irrespective of the line of therapy for the treatment of RAI-refractory DTC, whereas cabozantinib has only been approved as a second-line treatment. Adverse effects (AEs) such as hypertension are often seen with MKI treatment, but are generally well manageable. In this review, current clinical studies will be discussed, and the toxicity and safety of sorafenib, lenvatinib and cabozantinib treatment will be evaluated, with a focus on AE hypertension and its treatment options. In short, treatment-emergent hypertension (TE-HTN) occurs with all three drugs, but is usually well manageable and leads only to a few dose modifications or even discontinuations. This is emphasized by the fact that lenvatinib is widely considered the first-line drug of choice, despite its higher rate of TE-HTN.

摘要

分化型甲状腺癌(DTC)在常规接受甲状腺切除术、放射性碘(RAI)和甲状腺刺激激素抑制治疗时,预后通常良好,但有些肿瘤对 RAI 治疗产生耐药性,需要替代治疗。索拉非尼、仑伐替尼和卡博替尼是用于治疗 RAI 难治性 DTC 的多激酶抑制剂(MKIs)。这些药物通过抑制参与肿瘤发生和血管生成的不同受体酪氨酸激酶(RTKs),改善无进展生存期(PFS)和总生存期(OS)。索拉非尼和仑伐替尼均已被批准用于治疗 RAI 难治性 DTC,无论治疗线如何,而卡博替尼仅被批准作为二线治疗药物。与 MKI 治疗相关的不良反应(AE),如高血压,通常较为常见,但一般易于管理。在这篇综述中,将讨论目前的临床研究,并评估索拉非尼、仑伐替尼和卡博替尼治疗的毒性和安全性,重点关注 AE 高血压及其治疗选择。简而言之,这三种药物均会引发治疗后高血压(TE-HTN),但通常易于管理,仅导致少数剂量调整,甚至停药。仑伐替尼尽管 TE-HTN 发生率更高,但被广泛认为是一线治疗药物,这一事实也强调了这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dc7/8623313/3361f4aa57c7/ijms-22-12217-g001.jpg

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