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阿法替尼(BIBW 2992)

[Afatinib (BIBW 2992)].

作者信息

Prim N, Fore M, Mennecier B

机构信息

Service de pneumologie, pôle de pathologie thoracique, nouvel hôpital civil, hôpitaux universitaires de Strasbourg, 1, porte de l'Hôpital, 67091 Strasbourg cedex, France.

Service de pneumologie, pôle de pathologie thoracique, nouvel hôpital civil, hôpitaux universitaires de Strasbourg, 1, porte de l'Hôpital, 67091 Strasbourg cedex, France.

出版信息

Rev Pneumol Clin. 2014 Oct;70(5):279-85. doi: 10.1016/j.pneumo.2014.03.002. Epub 2014 May 27.

Abstract

Afatinib (BIBW 2992) is an irreversible multi-target HER receptor tyrosine kinase inhibitor developed in patients with advanced solid tumours. Several phase I studies were conducted in patients with non-small cell lung cancer (NSCLC), as a single agent or in combination. In further phase II or III studies, patients were selected based on the duration of response to first generation EGFR-TKI in previous line (supposed to have greater chance to have an activating EGFR mutation) or based directly on the EGFR activating mutation status. Here, we report and comment the main results of these studies in lung cancer patients. This drug has been approved by the Food and Drug Administration in June 2013 for the first-line treatment of patients with metastatic NSCLC whose tumours have EGFR mutation. In Europe, it has been approved in September 2013 in the same indication.

摘要

阿法替尼(BIBW 2992)是一种不可逆的多靶点HER受体酪氨酸激酶抑制剂,用于晚期实体瘤患者。开展了多项I期研究,以非小细胞肺癌(NSCLC)患者为对象,采用单药治疗或联合治疗。在后续的II期或III期研究中,根据患者对一线第一代EGFR-TKI的反应持续时间(假定有更大机会发生EGFR激活突变)或直接根据EGFR激活突变状态进行患者选择。在此,我们报告并评论这些针对肺癌患者的研究的主要结果。该药物于2013年6月获美国食品药品监督管理局批准,用于一线治疗肿瘤具有EGFR突变的转移性NSCLC患者。在欧洲,该药于2013年9月获批用于相同适应症。

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