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肾细胞癌的分子靶向治疗

Molecular targeting therapy for renal cell carcinoma.

作者信息

Eto Masatoshi, Naito Seiji

机构信息

Department of Urology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

出版信息

Int J Clin Oncol. 2006 Jun;11(3):209-13. doi: 10.1007/s10147-006-0577-2.

Abstract

Metastatic renal cell carcinoma (RCC) is currently one of the most treatment-resistant malignancies. However, significant advances in understanding the molecular mechanisms underlying RCC have led to the development of rationally designed therapies, which are now being tested clinically. To date, the vascular endothelial growth factor receptor (VEGFR) pathway has been the most promising target, and two agents (BAY 43-9006 and SU 11248) that inhibit not only VEGFR but also other receptors, including platelet-derived growth factor receptor (PDGFR), FMS-like tyrosine kinase 3 (FLT3), KIT, and Raf kinase, were recently approved by the FDA for advanced RCC. In addition, a phase III trial investigating the addition of VEGF inhibition to interferon alpha (IFN-alpha) in RCC is also now going on. Although the clinical activity of existing agents is to be further defined in ongoing trials, the exciting clinical response data with VEGF inhibition in RCC have demonstrated a key role in the treatment of this historically resistant malignancy.

摘要

转移性肾细胞癌(RCC)是目前最难治疗的恶性肿瘤之一。然而,在理解RCC潜在分子机制方面取得的重大进展促使了合理设计疗法的开发,目前这些疗法正在进行临床测试。迄今为止,血管内皮生长因子受体(VEGFR)途径一直是最有前景的靶点,两种不仅抑制VEGFR,还抑制包括血小板衍生生长因子受体(PDGFR)、FMS样酪氨酸激酶3(FLT3)、KIT和Raf激酶在内的其他受体的药物(BAY 43-9006和SU 11248)最近已获美国食品药品监督管理局(FDA)批准用于晚期RCC。此外,一项关于在RCC中添加VEGF抑制药物至α干扰素(IFN-α)的III期试验目前也在进行。尽管现有药物的临床活性将在正在进行的试验中进一步明确,但RCC中VEGF抑制药物令人振奋的临床反应数据已证明其在治疗这种历来难治的恶性肿瘤中发挥着关键作用。

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