前列腺癌
谷氨酸羧肽酶Ⅱ
单克隆抗体
抗体
癌症研究
前列腺
内化
抗原
结合
转移
医学
癌症
抗体-药物偶联物
免疫学
内科学
受体
数学分析
数学
作者
Michael D. Henry,Shenghua Wen,Matthew D. Silva,Sudeep Chandra,Mark Milton,Peter J. Worland
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2004-11-01
卷期号:64 (21): 7995-8001
被引量:153
标识
DOI:10.1158/0008-5472.can-04-1722
摘要
Abstract MLN2704 is an antibody-chemotherapeutic conjugate designed to target prostate-specific membrane antigen (PSMA). PSMA is a transmembrane receptor whose expression is largely restricted to prostatic epithelium and prostate cancer cells with its expression level increasing during the progression of malignancy. MLN2704 consists of a de-immunized, monoclonal antibody that is specific for PSMA conjugated to drug maytansinoid 1 (DM1), a microtubule-depolymerizing compound. After antibody binding to PSMA and the subsequent cellular internalization of this complex, DM1 is released leading to cell death. MLN2704 has an approximate half-life of 39 hours in scid mice bearing CWR22 tumor tissue, and the antibody effectively penetrates xenograft tumor tissue. Optimization of dosage and schedule of MLN2704 administration defined interdependency between these conditions that maximized efficacy with no apparent toxicity. Tumor growth delays of ∼100 days could be achieved on the optimized schedule of one dose of 60 mg/kg MLN2704 every 14 days for five doses (q14d×5). The unconjugated antibody (MLN591) demonstrated essentially no antitumor activity and DM1 alone or a non-PSMA targeted antibody–DM1 conjugate was only weakly active. Furthermore, we show that MLN2704 is active in a novel model of osteoblastic prostate cancer metastasis.
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