Targeted therapies in ovarian cancer: where we stand and where we are heading

被引:0
|
作者
Lee, Taek Sang [1 ]
机构
[1] SMG SNU Boramae Med Ctr, Dept Obstet & Gynecol, Seoul, South Korea
来源
关键词
Ovarian cancer; Molecular targeted therapy; Vascular endothelial growth factor; Poly(ADP-ribose) polymerase inhibitors; OPEN-LABEL; COMBINATION CEDIRANIB; EPITHELIAL OVARIAN; TUMOR ANGIOGENESIS; DOUBLE-BLIND; PHASE-I; RECURRENT; BEVACIZUMAB; CARCINOMA; OLAPARIB;
D O I
10.5124/jkma.2023.66.6.384
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Ovarian cancer is a highly lethal gynecological cancer globally. The standard treatment for this disease is cytoreductive surgery followed by platinum-based chemotherapy. However, most patients develop platinum resistance after multiple relapses and have an inadequate response to second-line chemotherapy. Additionally, molecular heterogeneity poses a challenge to effective treatment. Current Concepts: Advancements in understanding the molecular mechanisms of cancer progression provide insight into novel targeted therapies, which have emerged as groundbreaking and promising cancer treatment strategies. Poly(ADP-ribose) polymerase inhibitors and anti-vascular endothelial growth factor monoclonal antibodies are currently the two approved and most effective targeted drugs for ovarian cancer. Discussion and Conclusion: This review article discusses related clinical trials assessing the efficacy and safety of promising targets in ovarian cancer as well as challenges associated with targeted therapy, including drug resistance, heterogeneity, and toxicity. Additionally, possible solutions to optimize treatment effects are proposed. Targeting these molecular abnormalities will bring us closer to the goal of personalized therapy and improve the prognosis for patients with ovarian cancer.
引用
收藏
页码:384 / 392
页数:9
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