Immune Checkpoint Inhibition: Therapeutic Implications in Epithelial Ovarian Cancer

被引:12
作者
Longoria, Teresa C. [1 ]
Eskander, Ramez N. [1 ]
机构
[1] Univ Calif Irvine, Med Ctr, Dept Obstet & Gynecol, Div Gynecol Oncol, Orange, CA 92868 USA
关键词
Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4); immune checkpoint; immunoediting; ipilimumab; nivolumab; ovarian cancer; pembrolizumab; programmed cell death protein 1 (PD-1); LYMPHOCYTE-ASSOCIATED ANTIGEN-4; REGULATORY T-CELLS; ADVANCED MELANOMA; METASTATIC MELANOMA; ANTITUMOR IMMUNITY; ANTIBODY BLOCKADE; CLINICAL ACTIVITY; TUMOR-REGRESSION; CTLA-4; BLOCKADE; LUNG-CANCER;
D O I
10.2174/1574892810666150504121000
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ovarian cancer accounts for more deaths than any other gynecologic malignancy. According to the Ovarian Cancer National Alliance, overall mortality rates due to ovarian cancer have not significantly improved in 40 years, a statistic that highlights the need for innovative treatment strategies. Immune checkpoint inhibitors are part of an emerging immunotherapeutic model that seeks to "inhibit the inhibitors" of adequate cancer immunosurveillance. Immune checkpoints encompass a variety of inhibitory pathways that downregulate an immune response, which allows them to assume an important physiologic role in maintaining homeostasis. While cancer cells are adept at utilizing these pathways to their advantage, basic scientists, translational researchers, and clinical trialists are making great strides in this area of investigation. This review article will focus on the development of anti-CTLA-4 and anti-PD1 monoclonal antibodies, their current role in the treatment of advanced stage EOC, and recently published patents that incorporate the use of immune checkpoint inhibition in the treatment of cancer.
引用
收藏
页码:133 / 144
页数:12
相关论文
共 107 条
[1]   PD-L1 on Tumor Cells Is Induced in Ascites and Promotes Peritoneal Dissemination of Ovarian Cancer through CTL Dysfunction [J].
Abiko, Kaoru ;
Mandai, Masaki ;
Hamanishi, Junzo ;
Yoshioka, Yumiko ;
Matsumura, Noriomi ;
Baba, Tsukasa ;
Yamaguchi, Ken ;
Murakami, Ryusuke ;
Yamamoto, Ayaka ;
Kharma, Budiman ;
Kosaka, Kenzo ;
Konishi, Ikuo .
CLINICAL CANCER RESEARCH, 2013, 19 (06) :1363-1374
[2]   Tumor antigen-specific CD8 T cells infiltrating the tumor express high levels of PD-1 and are functionally impaired [J].
Ahmadzadeh, Mojgan ;
Johnson, Laura A. ;
Heemskerk, Bianca ;
Wunderlich, John R. ;
Dudley, Mark E. ;
White, Donald E. ;
Rosenberg, Steven A. .
BLOOD, 2009, 114 (08) :1537-1544
[3]  
[Anonymous], 2011, Obstet Gynecol, V117, P742, DOI 10.1097/AOG.0b013e31821477db
[4]  
[Anonymous], [No title captured]
[5]  
[Anonymous], [No title captured]
[6]  
[Anonymous], 29 ANN M SOC IMM CAN
[7]  
[Anonymous], [No title captured]
[8]  
[Anonymous], [No title captured]
[9]  
[Anonymous], [No title captured]
[10]  
[Anonymous], AM SOC CLIN ONC ANN