Antibody-Drug Conjugates in Cancer Therapy

被引:582
作者
Sievers, Eric L. [1 ]
Senter, Peter D. [1 ]
机构
[1] Seattle Genet, Bothell, WA 98021 USA
来源
ANNUAL REVIEW OF MEDICINE, VOL 64 | 2013年 / 64卷
关键词
immunotherapy; chemotherapeutic; monoclonal antibody; tumor; drug delivery; targeting; ACUTE MYELOID-LEUKEMIA; METASTATIC BREAST-CANCER; LARGE-CELL LYMPHOMA; GEMTUZUMAB OZOGAMICIN; MONOCLONAL-ANTIBODY; BRENTUXIMAB VEDOTIN; ANTITUMOR-ACTIVITY; PHASE-II; INOTUZUMAB OZOGAMICIN; HODGKIN LYMPHOMA;
D O I
10.1146/annurev-med-050311-201823
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
An antibody-drug conjugate (ADC) provides the possibility of selectively ablating cancer cells by combining the specificity of a monoclonal antibody (mAb) for a target antigen with the delivery of a highly potent cytotoxic agent. ADC target antigens are typically highly expressed on the surface of cancer cells compared to normal cells. The tumor target, the cytotoxic agent, and the manner in which the agent is attached to the antibody are key determinants of clinical activity and tolerability. Recently, several clinical trials have demonstrated that ADCs achieve higher clinical response rates than unconjugated mAbs targeting the same cell surface antigen. Brentuximab vedotin represents one such ADC that has recently been approved for the treatment of relapsed Hodgkin and systemic anaplastic large cell lymphomas-both characterized by high expression of the target antigen, CD30, on the surface of malignant cells. This review summarizes key characteristics of current, clinically active ADCs and highlights recent clinical data illustrating the benefit of antibody-targeted delivery of cytotoxic agents to cancer cells.
引用
收藏
页码:15 / 29
页数:15
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