Linked-In: Design and Efficacy of Antibody Drug Conjugates in Oncology

被引:33
作者
Feld, Jonathan [1 ]
Barta, Stefan K. [1 ]
Schinke, Carolina [1 ]
Braunschweig, Ira [1 ]
Zhou, Yiyu [1 ]
Verma, Amit K. [1 ]
机构
[1] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
关键词
antibody drug conjugates; oncotargets; immunotoxins; IMMUNOTOXIN RFB4(DSFV)-PE38 BL22; CMC-544 INOTUZUMAB OZOGAMICIN; CHRONIC LYMPHOCYTIC-LEUKEMIA; BRENTUXIMAB VEDOTIN SGN-35; RECOMBINANT IMMUNOTOXIN; PHASE-I; ANTI-CD22; IMMUNOTOXIN; ANTITUMOR-ACTIVITY; TARGETED CHEMOTHERAPY; TRASTUZUMAB EMTANSINE;
D O I
10.18632/oncotarget.924
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The use of antibody drug conjugates (ADCs) as targeted chemotherapies has successfully entered clinical practice and holds great promise. ADCs consist of an antibody and toxin-drug combined together via a chemical linker. While the antibody and drug are of vital importance in the direct elimination of cancer cells, more advanced linker technology was instrumental in the delivery of more potent drugs with fewer side effects. Here, we discuss the preclinical experience as well as clinical trials, with a specific emphasis on the clinical outcomes and side effects, in addition to linker strategies for five different ADCs, in order to describe different approaches in the development of this new class of anticancer agents. Brentuximab vedotin is approved for use in Hodgkin's lymphoma and Trastuzumab emtansine is approved for breast cancer. Combotox, Inotuzumab Ozogamicin, and Moxetumomab Pasudotox are in various stages of clinical development and are showing significant efficacy in lymphoid malignancies. These ADCs illustrate the promise and future potential of targeted therapy for presently incurable malignancies.
引用
收藏
页码:397 / 412
页数:16
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