Clinical translation of folate receptor-targeted therapeutics

被引:68
|
作者
Teng, Lesheng [1 ,2 ]
Xie, Jing [1 ,2 ]
Teng, Lirong [1 ]
Lee, Robert J. [1 ,2 ]
机构
[1] Jilin Univ, Inst Life Sci, Changchun 130023, Jili, Peoples R China
[2] Ohio State Univ, Coll Pharm, Div Pharmaceut, Columbus, OH 43210 USA
基金
美国国家科学基金会;
关键词
cancer; drug delivery; drug targeting; folate receptor; leukemia; HUMANIZED MONOCLONAL-ANTIBODY; OVARIAN-CANCER; DRUG-DELIVERY; ALPHA; EXPRESSION; CONJUGATE; BINDING; EC145; TISSUE; CELLS;
D O I
10.1517/17425247.2012.694863
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Folate receptor-alpha (FR-alpha) has been established as a membrane marker for ovarian cancer. In addition, it is frequently overexpressed in other major types of epithelial tumors. FR-alpha-based tumor-targeted therapy and drug carriers have been an active area of laboratory research for more than 20 years. Recently, there has been a great increase in the effort to finally translate this promising technology into the clinic and bring FR-targeted therapeutics into the market. Areas covered: Two FR-targeted therapeutic agents have moved into Phase III clinical trials, the monoclonal antibody farletuzumab and the low molecular weight vintafolide, combined with etarfolatide as a companion imaging agent, representing two alternative strategies for targeting the FR. Expert opinion: Each of the two strategies has advantages and disadvantages. Identification of the best target patient population is likely critical to the ultimate success of FR-targeted agents in the clinic. A successful clinical strategy may require the integration between FR expression analysis and an optimal combination of FR-targeted therapy and standard chemotherapy. Advancement into Phase III trials and the ongoing clinical development of several additional folate conjugates are likely to usher in a new era of clinical translation and validation of FR-targeted imaging and therapeutic agents.
引用
收藏
页码:901 / 908
页数:8
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