Han Ernest S, Lin Paul, Wakabayashi Mark
Division of Gynecologic Oncology, Department of Surgery, City of Hope, Duarte, CA 91010-3000, USA.
Curr Treat Options Oncol. 2009 Apr;10(1-2):54-66. doi: 10.1007/s11864-009-0100-x. Epub 2009 Apr 21.
Treatment of epithelial ovarian cancer generally involves surgical staging followed by chemotherapy with a combination of a platinum and a taxane-containing agent. However, a majority of patients recur and ultimately succumb to their cancer. Novel therapies that target specific pathways involved in ovarian tumorigenesis are rapidly emerging. In ovarian cancer, targeted therapies have focused on both the vascular endothelial growth factor (VEGF) and epidermal growth factor receptor (EGFR) pathways. Single-agent bevacizumab, a VEGF inhibitor, demonstrated significant clinical activity in multiple phase II studies. Various combinations of cytotoxic and biologic agents with bevacizumab as well as newer anti-angiogenesis agents are being tested. In contrast, EGFR inhibitors have not shared the same clinical activity in epithelial ovarian cancers as compared to the VEGF inhibitors. Translational studies are needed to help design rational combinations of targeted agents and to help predict response to therapy.
上皮性卵巢癌的治疗通常包括手术分期,随后使用铂类和含紫杉烷类药物联合进行化疗。然而,大多数患者会复发并最终死于癌症。针对卵巢肿瘤发生过程中特定途径的新型疗法正在迅速涌现。在卵巢癌中,靶向治疗主要集中在血管内皮生长因子(VEGF)和表皮生长因子受体(EGFR)途径。单克隆抗体贝伐单抗是一种VEGF抑制剂,在多项II期研究中显示出显著的临床活性。目前正在测试细胞毒性药物和生物制剂与贝伐单抗以及新型抗血管生成药物的各种联合应用。相比之下,与VEGF抑制剂相比,EGFR抑制剂在上皮性卵巢癌中并未表现出相同的临床活性。需要开展转化研究,以帮助设计合理的靶向药物联合方案,并帮助预测治疗反应。