布仑妥昔单抗维多汀
抗体-药物偶联物
细胞毒性T细胞
单克隆抗体
抗原
医学
癌症研究
抗体
癌细胞
癌症
CD30
肿瘤科
免疫学
内科学
生物
肿瘤细胞
体外
生物化学
作者
Eric L. Sievers,Peter D. Senter
标识
DOI:10.1146/annurev-med-050311-201823
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.
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