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尼达尼布治疗非小细胞肺癌:迄今的证据及在治疗中的地位。

Nintedanib in NSCLC: evidence to date and place in therapy.

作者信息

Bronte Giuseppe, Passiglia Francesco, Galvano Antonio, Barraco Nadia, Listì Angela, Castiglia Marta, Rizzo Sergio, Fiorentino Eugenio, Bazan Viviana, Russo Antonio

机构信息

Oncological and Oral Sciences, Section of Medical Oncology, University of Palermo, Italy.

Department of Surgical, Oncological and Oral Sciences, Section of Medical Oncology, University of Palermo, Via del Vespro 129, 90127 Palermo, Italy.

出版信息

Ther Adv Med Oncol. 2016 May;8(3):188-97. doi: 10.1177/1758834016630976. Epub 2016 Feb 16.

Abstract

The treatment of advanced non-small cell lung cancer (NSCLC) is currently driven by the detection of targetable oncogenic drivers, i.e. epidermal growth factor receptor, echinoderm microtubule-associated protein-like 4-anaplastic lymphoma kinase, etc. Those patients who are wildtype for known and valuable oncogenes can receive standard chemotherapy as first-line treatment, with the possibility of adding bevacizumab. With regard to second-line treatment, nintedanib can improve the efficacy of docetaxel. Nintedanib is a tyrosine kinase inhibitor targeting three angiogenesis-related transmembrane receptors. The usefulness of nintedanib as an anticancer agent for NSCLC has been proved by both preclinical and clinical phase I and II trials; however, its approval for the use in clinical practice has been possible because of the positive results of the LUME-Lung 1 trial (nintedanib + docetaxel versus docetaxel alone) in terms of progression-free survival and overall survival, and a manageable tolerability profile. Therefore, the good results seen in the clinical trials with nintedanib in the second-line setting for NSCLC patients with adenocarcinoma subtype are encouraging enough to recommend it in clinical practice.

摘要

目前,晚期非小细胞肺癌(NSCLC)的治疗取决于可靶向致癌驱动因子的检测,即表皮生长因子受体、棘皮动物微管相关蛋白样4-间变性淋巴瘤激酶等。那些已知有价值的致癌基因呈野生型的患者可接受标准化疗作为一线治疗,并有可能加用贝伐单抗。关于二线治疗,尼达尼布可提高多西他赛的疗效。尼达尼布是一种靶向三种血管生成相关跨膜受体的酪氨酸激酶抑制剂。临床前以及临床I期和II期试验均已证明尼达尼布作为NSCLC抗癌药物的有效性;然而,由于LUME-Lung 1试验(尼达尼布+多西他赛对比单用多西他赛)在无进展生存期和总生存期方面取得了阳性结果,且耐受性可控,其才得以获批用于临床实践。因此,在腺癌亚型NSCLC患者的二线治疗中,尼达尼布在临床试验中取得的良好结果足以令人鼓舞,从而推荐其在临床实践中应用。

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