Emerging immunotherapy strategies in breast cancer

被引:2
作者
Page, David B. [1 ]
Naidoo, Jarushka [1 ]
McArthur, Heather L. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10065 USA
关键词
adoptive therapy; breast cancer; immunotherapy; ipilimumab; nivolumab; trastuzumab; tremelimumab; ABERRANTLY GLYCOSYLATED MUC1; METASTATIC BREAST; T-CELLS; CTLA-4; BLOCKADE; OPEN-LABEL; OVEREXPRESSING BREAST; MONOCLONAL-ANTIBODY; IMMUNE CHECKPOINT; MELANOMA PATIENTS; ADVERSE EVENTS;
D O I
10.2217/IMT.13.166
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although immunogenicity is typically associated with renal cell carcinomas and melanoma, there are several compelling reasons why immune-based therapies should be explored in breast cancer. First, breast cancers express multiple putative tumor-associated antigens, such as HER-2 and MUC-1, which have been the successful focus of vaccine development over the past decade, translating into tumor-specific immune responses and, in some cases, clinical benefit. Second, passive immune strategies with anti-HER-2 antibodies, such as trastuzumab and pertuzumab, have led to survival benefits in breast cancer. Finally, the successes observed with novel immunotherapeutic strategies, such as immune checkpoint blockade and adoptive T-cell therapies in other malignancies, combined with a growing body of literature that supports an interplay between solid tumors and the immune system, indicate that these strategies have the potential to revolutionize the treatment of breast cancer.
引用
收藏
页码:195 / 209
页数:15
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