伊立替康
医学
抗体-药物偶联物
序号38
癌症
体内
前药
药代动力学
结合
药理学
抗体
癌症研究
肿瘤科
单克隆抗体
内科学
结直肠癌
免疫学
生物
生物技术
数学分析
数学
作者
David M. Goldenberg,Thomas M. Cardillo,Serengulam V. Govindan,Edmund A. Rossi,Robert M. Sharkey
出处
期刊:Oncotarget
[Impact Journals LLC]
日期:2015-06-18
卷期号:6 (26): 22496-22512
被引量:433
标识
DOI:10.18632/oncotarget.4318
摘要
Trop-2 is a novel target for ADC therapy because of its high expression by many solid cancers. The rational development of IMMU-132 represents a paradigm shift as an ADC that binds a well-known moderately-cytotoxic drug, SN-38, to the anti-Trop-2 antibody. In vitro and in vivo studies show enhanced efficacy, while there is a gradual release of SN-38 that contributes to the overall effect. IMMU-132 is most efficacious at a high drug:antibody ratio (DAR) of 7.6:1, which does not affect binding and pharmacokinetics. It targets up to 136-fold more SN-38 to a human cancer xenograft than irinotecan, SN-38's prodrug. IMMU-132 delivers SN-38 in its most active, non-glucuronidated form, which may explain the lower frequency of severe diarrhea than with irinotecan. Thus, this ADC, carrying a moderately-toxic drug targeting Trop-2 represents a novel cancer therapeutic that is showing promising activity in patients with several metastatic cancer types, including triple-negative breast cancer, non-small-cell and small-cell lung cancers.
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