Active immunotherapy in HER2 overexpressing breast cancer: current status and future perspectives

被引:72
作者
Milani, A. [1 ,2 ]
Sangiolo, D. [1 ,2 ]
Montemurro, F. [1 ,3 ]
Aglietta, M. [1 ,2 ]
Valabrega, G. [1 ,2 ]
机构
[1] FPO, Inst Canc Res & Treatment IRCC Candiolo, I-10060 Turin, Italy
[2] Univ Torino, Dept Oncol, Sch Med, Candiolo, Italy
[3] Investigative Clin Oncol Unit INCO, Candiolo, Italy
关键词
active immunotherapy; breast cancer; HER2; vaccine; GROUP-STUDY I-01; COLONY-STIMULATING FACTOR; CYTOTOXIC T-LYMPHOCYTES; I CLINICAL-TRIAL; METASTATIC BREAST; E75; VACCINE; PEPTIDE VACCINE; ADJUVANT CHEMOTHERAPY; IMMUNE-RESPONSE; TUMOR-ANTIGEN;
D O I
10.1093/annonc/mdt133
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The use of anti-HER2 monoclonal antibodies (mAbs) has improved the clinical outcome of HER2-overexpressing breast cancers (BCs). Unfortunately, often these tumors tend to relapse and, when metastatic, the duration of clinical benefit is limited over time and almost invariably followed by tumor progression. Alternative approaches to this essentially passive immunotherapy are therefore needed in HER2-overexpressing BC patients. As HER2 is one of the most suitable targets for active immunotherapy in BC, manipulating the immune system is a highly attractive approach. Material and methods: A computer-based literature search was carried out using PubMed (keywords: breast neoplasm, HER2 vaccine, immunology); data reported at international meetings were included. Results: This review provides a focus on the following active vaccinal approaches under clinical investigation against HER2-overexpressing BC: (i) peptide and protein based; (ii) DNA based; (iii) whole tumor cell based; (iv) dendritic cell based. Moreover, the review discuss future challenges in the field, trying to define the best setting for the development of this innovative strategy, considering both immunological and clinical aspects of HER2 targeting. Conclusions: Development of effective vaccines for BC remains a distinct challenge but is likely to become a substantial advance for patients with HER2-overexpressing BCs.
引用
收藏
页码:1740 / 1748
页数:9
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