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新型抗血管生成药物在非小细胞肺癌治疗中的应用:瓦格鲁(BIBF 1120)及其他药物。

New antiangiogenics in non-small cell lung cancer treatment: Vargatef™ (BIBF 1120) and beyond.

机构信息

Oncological-Pulmonary Unit 1st, San Camillo Hospital, Rome, Italy.

出版信息

Ther Clin Risk Manag. 2011;7:429-40. doi: 10.2147/TCRM.S22079. Epub 2011 Nov 17.

Abstract

Lung cancer is the leading cause of mortality worldwide. Non-small cell lung cancer (NSCLC) is a particularly aggressive cancer, the optimum management of which is still being determined. In the metastatic disease, the standard therapy is a platinum-based combination chemotherapy; however, in spite of available treatment options for patients who progress beyond first-line therapy, prognosis remains poor. Angiogenesis is a tightly regulated process which comprises a complex, complementary, and overlapping network. Inhibition of tumor-related angiogenesis has become an attractive target for anticancer therapy. Antiangiogenic strategy includes: monoclonal antibodies against vascular endothelial growth factor (VEGF) and VEGF receptor (VEGFR), small molecule inhibitors of VEGF tyrosine kinase activity, VEGF Trap, and a new class named "vascular disrupting agents," tested in ongoing clinical trials which will further define their role in the management of NSCLC. BIBF 1120 is an investigational orally administered receptor tyrosine kinase inhibitor that has shown antiangiogenic and antineoplastic activity, inhibiting VEGFR, platelet-derived growth factor receptor, and fibroblast growth factor receptor tyrosine kinases, preventing tumor growth and interfering with the angiogenesis-signaling cascade and overcoming drug resistances.

摘要

肺癌是全球范围内导致死亡的主要原因。非小细胞肺癌(NSCLC)是一种特别具有侵袭性的癌症,其最佳治疗方法仍在确定中。在转移性疾病中,标准治疗是基于铂的联合化疗;然而,尽管有针对一线治疗后进展的患者的可用治疗选择,预后仍然很差。血管生成是一个受严格调控的过程,包括一个复杂、互补和重叠的网络。抑制肿瘤相关的血管生成已成为抗癌治疗的一个有吸引力的目标。抗血管生成策略包括:针对血管内皮生长因子(VEGF)和血管内皮生长因子受体(VEGFR)的单克隆抗体、VEGF 酪氨酸激酶活性的小分子抑制剂、VEGF 陷阱,以及一类名为“血管破坏剂”的新型药物,正在进行的临床试验进一步确定了它们在 NSCLC 治疗中的作用。BIBF 1120 是一种研究性的口服受体酪氨酸激酶抑制剂,具有抗血管生成和抗肿瘤活性,抑制 VEGFR、血小板衍生生长因子受体和成纤维细胞生长因子受体酪氨酸激酶,阻止肿瘤生长并干扰血管生成信号级联,克服药物耐药性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f9b/3253753/795af8249531/tcrm-7-429f1.jpg

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