Gubbi Ajit, Kendrick James E, Finkler Neil J
Florida Hospital Cancer Institute - Gynecologic Oncology, 2501 North Orange Ave, Orlando, Florida 32804, USA.
Expert Rev Anticancer Ther. 2014 Oct;14(10):1105-13. doi: 10.1586/14737140.2014.956095. Epub 2014 Sep 4.
The majority of women with ovarian cancer will experience a recurrence of their disease despite aggressive primary cytoreduction and adjuvant cytotoxic chemotherapy. Notwithstanding the high rate of recurrence, targeted and biologic agents have helped to decrease the dependence on cytotoxic chemotherapy. Bevacizumab, a vascular endothelial growth factor inhibitor, has been shown to cause regression in tumor vasculature, inhibition of angiogenesis and prevention of progenitor cell recruitment. Phase III clinical trials of bevacizumab in patients with primary epithelial ovarian cancer and in patients with platinum-sensitive ovarian cancer have shown an improvement in progression free survival without an appreciable difference in overall survival. The addition of bevacizumab to standard cytotoxic chemotherapy regimens has demonstrated improved response rates, and improved progression free survival. These results have stimulated research in additional angiogenesis inhibitors and trials to further incorporate bevacizumab into the treatment schema for patients with recurrent ovarian cancer.
尽管进行了积极的初次肿瘤细胞减灭术和辅助细胞毒性化疗,但大多数卵巢癌女性患者仍会出现疾病复发。尽管复发率很高,但靶向药物和生物制剂有助于减少对细胞毒性化疗的依赖。贝伐单抗是一种血管内皮生长因子抑制剂,已被证明可导致肿瘤血管消退、抑制血管生成并防止祖细胞募集。贝伐单抗在原发性上皮性卵巢癌患者和铂敏感型卵巢癌患者中的III期临床试验表明,无进展生存期有所改善,总生存期无明显差异。在标准细胞毒性化疗方案中添加贝伐单抗已证明有效率提高,无进展生存期延长。这些结果激发了对其他血管生成抑制剂的研究,并开展了相关试验,以进一步将贝伐单抗纳入复发性卵巢癌患者的治疗方案。