Bevacizumab use in the frontline, maintenance and recurrent settings for ovarian cancer

被引:70
作者
Haunschild, Carolyn E. [1 ,2 ]
Tewari, Krishnansu S. [2 ,3 ]
机构
[1] Univ Calif Irvine, Dept Obstet & Gynecol, 333 City Blvd West,Suite 1400, Orange, CA 92868 USA
[2] Univ Calif Irvine, Div Gynecol Oncol, 333 City Blvd West,Suite 1400, Orange, CA 92868 USA
[3] Univ Calif Irvine, Dept Obstet Gynecol, City Tower,333 City Blvd,West Suite 1400, Orange, CA 92868 USA
关键词
bevacizumab; biological therapy; clinical trials; gynecologic; ovarian; GYNECOLOGIC-ONCOLOGY-GROUP; PHASE-III TRIAL; PEGYLATED LIPOSOMAL DOXORUBICIN; ADVANCED EPITHELIAL OVARIAN; INTERVAL DEBULKING SURGERY; PRIMARY PERITONEAL; OPEN-LABEL; FALLOPIAN-TUBE; INTRAPERITONEAL CISPLATIN; NEOADJUVANT CHEMOTHERAPY;
D O I
10.2217/fon-2019-0042
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
On 13 June 2018, Genentech, Inc. issued a press release announcing that the US FDA had approved the antiangiogenesis drug, bevacizumab, in combination with chemotherapy for frontline and maintenance therapy for women with newly diagnosed ovarian cancer. Regulatory approval was based on the National Cancer Institute-sponsored Gynecologic Oncology Group (GOG) protocol 0218, the Phase III, randomized, placebo-controlled, double-blind, multi-center and multi-national clinical trial that met its primary end point, progression-free survival. Bevacizumab is now approved in the frontline, platinum-sensitive recurrent and platinum-resistant recurrent settings for epithelial ovarian cancer. This review will address the broad range of clinical trials addressing the efficacy of bevacizumab use in ovarian cancer.
引用
收藏
页码:225 / 246
页数:22
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