...
首页> 外文期刊>Journal of Ovarian Research >Bevacizumab in combination with chemotherapy for the treatment of advanced ovarian cancer: a systematic review
【24h】

Bevacizumab in combination with chemotherapy for the treatment of advanced ovarian cancer: a systematic review

机译:贝伐单抗联合化疗治疗晚期卵巢癌:系统评价

获取原文
           

摘要

As increased angiogenesis has been linked with the progression of ovarian cancer, a number of anti-angiogenic agents have been investigated, or are currently in development, as potential treatment options for patients with advanced disease. Bevacizumab, a recombinant monoclonal antibody against vascular endothelial growth factor, has gained European Medicines Agency approval for the front-line treatment of advanced epithelial ovarian cancer, fallopian tube cancer or primary peritoneal cancer in combination with carboplatin and paclitaxel, and for the treatment of first recurrence of platinum-sensitive ovarian cancer in combination with carboplatin and gemcitabine. We conducted a systematic literature review to identify available efficacy and safety data for bevacizumab in ovarian cancer as well as for newer anti-angiogenic agents in development. We analyzed published data from randomized, controlled phase II/III clinical trials enrolling women with ovarian cancer to receive treatment with bevacizumab. We also reviewed available data for emerging anti-angiogenic agents currently in phase II/III development, including trebananib, aflibercept, nintedanib, cediranib, imatinib, pazopanib, sorafenib and sunitinib. Significant efficacy gains were achieved with the addition of bevacizumab to standard chemotherapy in four randomized, double-blind, phase III trials, both as front-line treatment (GOG-0218 and ICON7) and in patients with recurrent disease (OCEANS and AURELIA). The type and frequency of bevacizumab-related adverse events was as expected in these studies based on published data. Promising efficacy data have been published for a number of emerging anti-angiogenic agents in phase III development for advanced ovarian cancer. Further research is needed to identify predictive or prognostic markers of response to bevacizumab in order to optimize patient selection and treatment benefit. Data from phase III trials of newer anti-angiogenic agents in ovarian cancer are awaited.
机译:由于增加的血管生成与卵巢癌的发展有关,因此已经研究或目前正在开发许多抗血管生成剂,作为晚期疾病患者的潜在治疗选择。贝伐单抗是一种抗血管内皮生长因子的重组单克隆抗体,已获得欧洲药品管理局的批准,可与卡铂和紫杉醇联合用于晚期上皮性卵巢癌,输卵管癌或原发性腹膜癌的一线治疗,铂敏感性卵巢癌与卡铂和吉西他滨合用的复发。我们进行了系统的文献综述,以鉴定贝伐单抗在卵巢癌以及正在开发的新型抗血管生成剂中的可用疗效和安全性数据。我们分析了来自卵巢癌女性接受贝伐单抗治疗的随机,对照II / III期临床试验的公开数据。我们还审查了目前处于II / III期开发阶段的新兴抗血管生成药物的可用数据,包括曲巴尼单抗,阿柏西普,nintedanib,西地尼单抗,伊马替尼,帕唑帕尼,索拉非尼和舒尼替尼。在四项随机,双盲,III期试验中,将贝伐单抗加入标准化疗中获得了显着的疗效提高,无论是作为一线治疗(GOG-0218和ICON7)还是复发性疾病患者(OCEANS和AURELIA)。与贝伐单抗相关的不良事件的类型和发生频率与这些研究基于公开数据的预期相同。在晚期卵巢癌的III期开发中,许多新兴的抗血管生成药物的疗效数据已经发表。为了进一步优化患者选择和治疗获益,需要进一步的研究来确定贝伐单抗反应的预测或预后指标。等待来自卵巢癌中新的抗血管生成剂的III期试验数据。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号