阿西替尼治疗转移性肾细胞癌。

Biologics in therapy Pub Date : 2012-10-16 eCollection Date: 2012-01-01 DOI:10.1007/s13554-012-0005-2
Kriti Mittal, Laura S Wood, Brian I Rini
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引用次数: 11

摘要

靶向药物彻底改变了转移性肾细胞癌(RCC)的治疗。阿西替尼(Axitinib)是一种血管内皮生长因子受体(VEGFR)抑制剂,是目前晚期RCC治疗的重要补充。它在纳摩尔浓度下抑制vegfr的能力使其成为一种有效的酪氨酸激酶抑制剂,在临床适用浓度下对VEGFR-1、2和3具有更高的选择性。3期AXIS试验已经确立了其在延长既往治疗的RCC患者无进展生存期(PFS)方面的优势(阿西替尼的中位PFS为6.7个月,索拉非尼的中位PFS为4.7个月)。阿西替尼的常见毒性包括高血压、腹泻、恶心、手足综合征、疲劳和甲状腺功能减退。阿西替尼诱导的舒张压升高可能与改善的临床结果相关,可能反映了阿西替尼的“靶标”效应。剂量递增以达到治疗血浆药物水平是相当重要的临床兴趣。虽然阿西替尼在以前用一种药物治疗的患者中已经建立了疗效,但它在一线环境中的使用目前是正在进行的研究的主题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Axitinib in Metastatic Renal Cell Carcinoma.

Targeted agents have revolutionized the management of metastatic renal cell carcinoma (RCC). Axitinib, an inhibitor of vascular endothelial growth factor receptor (VEGFR), has been an important addition to currently available therapies for advanced RCC. Its ability to inhibit VEGFRs at nanomolar concentrations distinguishes it as a potent tyrosine kinase inhibitor, with increased selectivity for VEGFR-1, 2, and 3 at clinically applicable concentrations. The phase 3 AXIS trial has established its superiority in prolonging progression-free survival (PFS) in previously treated RCC patients (median PFS 6.7 months for axitinib vs. 4.7 months for sorafenib). Common toxicities of axitinib include hypertension, diarrhea, nausea, hand-foot syndrome, fatigue, and hypothyroidism. Axitinib-induced diastolic blood pressure elevation may be associated with improved clinical outcome, likely reflecting the "on-target" effect of axitinib. Dose escalation to achieve therapeutic plasma drug levels is of considerable clinical interest. Although axitinib has established efficacy in patients treated with one previous agent, its use in the frontline setting is currently the subject of ongoing research.

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