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非小细胞肺癌二线和三线治疗中分子靶向治疗的最新进展:聚焦 EGFR 抑制剂和抗血管生成药物。

An update on molecularly targeted therapies in second- and third-line treatment in non-small cell lung cancer: focus on EGFR inhibitors and anti-angiogenic agents.

机构信息

Medical Oncology Service, Hospital de la Santa Creu i Sant Pau, c/Sant Antoni Maria Claret 167, 08025, Barcelona, Spain.

出版信息

Clin Transl Oncol. 2013 May;15(5):343-57. doi: 10.1007/s12094-012-0964-2. Epub 2013 Jan 29.

DOI:10.1007/s12094-012-0964-2
PMID:23359171
Abstract

Docetaxel, pemetrexed and epidermal growth factor receptor tyrosine kinase inhibitors (gefitinib and erlotinib) are recommended second-line therapy for advanced non-small cell lung cancer (NSCLC) patients with disease progression. Although erlotinib is the only recommended third-line therapy, several drugs are being used in the clinic. Recent studies have focused on combining targeted agents with approved therapies, including broad-spectrum multikinase inhibitors targeting multiple ErbB Family receptors and multitargeted anti-angiogenic agents targeting the vascular endothelial growth factor receptor, platelet-derived growth factor receptor and fibroblast growth factor receptor pathways. Here, we review targeted therapies that are being evaluated in second- and third-line settings in NSCLC, including the ErbB Family Blocker afatinib (BIBW 2992), multityrosine kinase inhibitors (pelitinib [EKB-56]), neratinib [HKI-272], canertinib [CI-1033], lapatinib [GW-572016], dacomitinib [PF-299804]) and multitargeted anti-angiogenic agents (vandetanib [ZD6474], sunitinib [SU11248], sorafenib [BAY43-9006], nintedanib [BIBF1120], axitinib [AG-013736], cediranib [AZD2171], motesanib [AMG 706], linifanib [ABT869] and pazopanib [GW786034]).

摘要

多西他赛、培美曲塞和表皮生长因子受体酪氨酸激酶抑制剂(吉非替尼和厄洛替尼)被推荐用于疾病进展的晚期非小细胞肺癌(NSCLC)患者的二线治疗。虽然厄洛替尼是唯一推荐的三线治疗药物,但临床上也有几种药物在使用。最近的研究集中在将靶向药物与已批准的治疗方法联合使用,包括针对多个 ErbB 家族受体的广谱多激酶抑制剂和针对血管内皮生长因子受体、血小板衍生生长因子受体和成纤维细胞生长因子受体途径的多靶点抗血管生成药物。在这里,我们综述了正在 NSCLC 二线和三线治疗中评估的靶向治疗药物,包括 ErbB 家族阻滞剂阿法替尼(BIBW 2992)、多酪氨酸激酶抑制剂(培立替尼[EKB-56])、奈拉替尼[HKI-272]、卡奈替尼[CI-1033]、拉帕替尼[GW-572016]、达克替尼[PF-299804]和多靶点抗血管生成药物(凡德他尼[ZD6474]、舒尼替尼[SU11248]、索拉非尼[BAY43-9006]、尼达尼布[BIBF1120]、阿昔替尼[AG-013736]、西地尼布[AZD2171]、莫特塞尼布[AMG 706]、linifanib [ABT869]和帕唑帕尼[GW786034])。

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本文引用的文献

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吲哚连接的嘧啶衍生物同时抑制表皮生长因子受体和其他血管生成激酶的构效关系
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Response to alectinib after one year of discontinuation of crizotinib in anaplastic lymphoma kinase-positive non-small-cell lung cancer: A case report.间变性淋巴瘤激酶阳性非小细胞肺癌患者停用克唑替尼一年后对阿来替尼的反应:一例报告
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Canertinib induces ototoxicity in three preclinical models.卡奈替尼在三种临床前模型中诱发耳毒性。
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Afatinib for patients with lung adenocarcinoma and epidermal growth factor receptor mutations (LUX-Lung 2): a phase 2 trial.阿法替尼治疗表皮生长因子受体突变的肺腺癌患者(LUX-Lung 2):一项 2 期临床试验。
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Vandetanib Versus placebo in patients with advanced non-small-cell lung cancer after prior therapy with an epidermal growth factor receptor tyrosine kinase inhibitor: a randomized, double-blind phase III trial (ZEPHYR).凡德他尼与安慰剂在表皮生长因子受体酪氨酸激酶抑制剂治疗后进展的晚期非小细胞肺癌患者中的比较:一项随机、双盲 III 期试验(ZEPHYR)。
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The effect of dacomitinib (PF-00299804) on CYP2D6 activity in healthy volunteers who are extensive or intermediate metabolizers.达可替尼(PF-00299804)对 CYP2D6 活性的影响,在广泛代谢者或中间代谢者的健康志愿者中。
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Afatinib (BIBW 2992) development in non-small-cell lung cancer.阿法替尼(BIBW 2992)在非小细胞肺癌中的研发。
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Phase II study of sunitinib in patients with non-small cell lung cancer and irradiated brain metastases.舒尼替尼治疗非小细胞肺癌伴脑转移放疗患者的 II 期研究。
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