Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
Cytokine Growth Factor Rev. 2010 Feb;21(1):21-6. doi: 10.1016/j.cytogfr.2009.11.003. Epub 2009 Dec 11.
FDA approval of several inhibitors of the VEGF pathway has enabled significant advances in the therapy of cancer and neovascular age-related macular degeneration. However, similar to other therapies, inherent/acquired resistance to anti-angiogenic drugs may occur in patients, leading to disease progression. So far the lack of predictive biomarkers has precluded identification of patients most likely to respond to such treatments. Recent suggest that both tumor and non-tumor (stromal) cell types are involved in the reduced responsiveness to the treatments. The present review examines the role of tumor- as well as stromal cell-derived pathways involved in tumor growth and in refractoriness to anti-VEGF therapies.
美国食品和药物管理局(FDA)批准了几种血管内皮生长因子(VEGF)通路抑制剂,这使得癌症和新生血管性年龄相关性黄斑变性的治疗取得了重大进展。然而,与其他疗法类似,患者可能会对抗血管生成药物产生内在/获得性耐药,从而导致疾病进展。到目前为止,缺乏预测性生物标志物使得无法确定最有可能对这些治疗有反应的患者。最近的研究表明,肿瘤和非肿瘤(基质)细胞类型都参与了对这些治疗的反应降低。本综述检查了肿瘤和基质细胞衍生的途径在肿瘤生长和对抗 VEGF 治疗的耐药性中的作用。