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首页> 外文期刊>OncoTargets and therapy >Lenvatinib and other tyrosine kinase inhibitors for the treatment of radioiodine refractory, advanced, and progressive thyroid cancer
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Lenvatinib and other tyrosine kinase inhibitors for the treatment of radioiodine refractory, advanced, and progressive thyroid cancer

机译:Lenvatinib和其他酪氨酸激酶抑制剂用于治疗难治性,晚期和进行性甲状腺癌的放射性碘

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摘要

Lenvatinib is a small oral molecule able to inhibit three of the extracellular and intracellular molecules involved in the modulation of angiogenesis and lymphangiogenesis: vascular endothelial growth factor receptor 1–3, fibroblast growth factor receptor 1–4, and platelet-derived growth factor receptor alpha. Since it is also able to inhibit the REarranged during Transfection oncogene and the protooncogene c-KIT , this drug can also be used to control tumor cell proliferation. The maximum tolerated dose, as demonstrated in Phase I studies, is 25 mg daily. The drug is rapidly absorbed with maximum concentrations achieved within 3 and 5 hours after administration in fasting and nonfasting treated patients, respectively. The most common adverse events, reported in Phase I study and confirmed in the subsequent Phase II and III studies, are hypertension, proteinuria, and gastrointestinal symptoms such as nausea, diarrhea, and stomatitis. In Phase I studies, efficacy of lenvatinib in solid tumors was demonstrated, and these encouraging results have led to the development of a Phase II study using lenvatinib in advance radioiodine-refractory differentiated thyroid cancer (DTCs) patients. Since an overall response rate of 50% was reported, this study also confirmed the efficacy of lenvatinib in DTCs patients with an acceptable toxicity profile. Recently, a Phase III study in patients with DTCs (SELECT study) demonstrated the lenvatinib efficacy in prolonging progression-free survival with respect to the placebo (18.3 vs 3.6 months; P 65?years). The study confirmed that the most common side effects of this drug are hypertension, diarrhea, decreased appetite, weight loss, nausea, and proteinuria. In this review, we report the results of the main studies on lenvatinib efficacy in patients with advanced and progressive thyroid cancer, mainly in DTCs but also in medullary and anaplastic thyroid cancer. We also compared the efficacy of lenvatinib with that of other tyrosine kinase inhibitors, mainly sorafenib, already tested in the same type of patient population.
机译:Lenvatinib是一种小型口服分子,能够抑制涉及血管生成和淋巴管生成调节的三种细胞外和细胞内分子:血管内皮生长因子受体1-3,成纤维细胞生长因子受体1-4和血小板衍生生长因子受体α 。由于它也能抑制转染癌基因和原癌基因c-KIT期间的重排,因此该药也可用于控制肿瘤细胞的增殖。如第一期研究所示,最大耐受剂量为每天25 mg。在禁食和非禁食治疗的患者中,药物分别在给药后3到5个小时内迅速吸收并达到最大浓度。在I期研究中报告并在随后的II和III期研究中证实的最常见不良事件是高血压,蛋白尿和胃肠道症状,例如恶心,腹泻和口腔炎。在I期研究中,证明了lenvatinib在实体瘤中的功效,这些令人鼓舞的结果已导致使用lenvatinib在放射性碘难治性分化型甲状腺癌(DTC)预先患者中进行II期研究。由于报告的总缓解率为50%,因此该研究还证实了lenvatinib在具有可接受毒性谱的DTC患者中的疗效。最近,一项针对DTC患者的III期研究(SELECT研究)表明,与安慰剂相比,lenvatinib可以延长无进展生存期(18.3 vs 3.6个月; P 65岁)。研究证实,这种药物最常见的副作用是高血压,腹泻,食欲下降,体重减轻,恶心和蛋白尿。在本综述中,我们报告了lenvatinib在晚期和进行性甲状腺癌患者中的主要研究结果,主要在DTC中,而且在髓样和间变性甲状腺癌中也是如此。我们还比较了lenvatinib与其他酪氨酸激酶抑制剂(主要是索拉非尼)的功效,这些抑制剂已经在相同类型的患者人群中进行了测试。

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