Prospects of chimeric antigen receptor T cell therapy in ovarian cancer

被引:18
作者
Jindal, Vishal [1 ]
Arora, Ena [2 ]
Gupta, Sorab [4 ]
Lal, Amos [1 ]
Masab, Muhammad [3 ]
Potdar, Rashmika [4 ]
机构
[1] St Vincent Hosp, Dept Internal Med, 123 Summer St, Worcester, MA 01608 USA
[2] Govt Med Coll & Hosp, Dept Internal Med, Chandigarh, India
[3] Einstein Healthcare Network, Dept Internal Med, Philadelphia, PA USA
[4] Einstein Healthcare Network, Dept Hematol & Oncol, Philadelphia, PA USA
关键词
Ovarian cancer; Chimeric antigen receptor; Immunotherapy; TUMOR-INFILTRATING LYMPHOCYTES; ANTITUMOR-ACTIVITY; ADOPTIVE TRANSFER; FOLATE RECEPTOR; PHASE-I; MONOCLONAL-ANTIBODY; MALIGNANT-CELLS; MESOTHELIN; EXPRESSION; MUC16;
D O I
10.1007/s12032-018-1131-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite advances in various chemotherapy regimens, current therapeutic options are limited for ovarian cancer patients. Immunotherapy provides a promising and novel treatment option for ovarian cancer. Recently, chimeric antigen receptor (CAR) T cell therapy has shown promising results in hematological tumors and current research is going on in various solid tumors like ovarian cancer. CAR T cells are genetically engineered T cells with major histocompatibility complexindependent, tumor-specific, immune-mediated cytolytic actions against cancer cells. Initial studies of CAR T cell therapy have shown promising results in ovarian cancer, but there are some obstacles like impaired T cell trafficking, lack of antigenic targets, cytokine release syndrome and most important immunosuppressive tumor microenvironment. Optimization of design, improving tumor microenvironment and combinations with other therapies may help us in improving CAR T cell efficacy. In this review article, we highlight the current knowledge regarding CAR T cell therapy in ovarian cancer. We have discussed basic functioning of CAR T cells, their rationale and clinical outcome in ovarian cancer with limitations.
引用
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页数:8
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