Henry Michael D, Wen Shenghua, Silva Matthew D, Chandra Sudeep, Milton Mark, Worland Peter J
Department of Cancer Pharmacology, Millennium Pharmaceuticals, Inc., Cambridge, Massachusetts 02139, USA.
Cancer Res. 2004 Nov 1;64(21):7995-8001. doi: 10.1158/0008-5472.CAN-04-1722.
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 approximately 100 days could be achieved on the optimized schedule of one dose of 60 mg/kg MLN2704 every 14 days for five doses (q14dx5). 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.
MLN2704是一种抗体-化疗偶联物,设计用于靶向前列腺特异性膜抗原(PSMA)。PSMA是一种跨膜受体,其表达主要局限于前列腺上皮和前列腺癌细胞,并且在恶性肿瘤进展过程中其表达水平会升高。MLN2704由一种去免疫的、对PSMA特异的单克隆抗体组成,该抗体与药物美登素1(DM1,一种微管解聚化合物)偶联。抗体与PSMA结合并使该复合物随后被细胞内化后,DM1被释放,导致细胞死亡。在携带CWR22肿瘤组织的重度联合免疫缺陷小鼠中,MLN2704的半衰期约为39小时,并且该抗体可有效穿透异种移植肿瘤组织。MLN2704给药剂量和方案的优化确定了这些条件之间的相互依赖性,即在无明显毒性的情况下使疗效最大化。按照每14天给予一剂60 mg/kg MLN2704,共五剂(q14dx5)的优化方案,可使肿瘤生长延迟约100天。未偶联的抗体(MLN591)基本无抗肿瘤活性,单独的DM1或非PSMA靶向的抗体-DM1偶联物仅有微弱活性。此外,我们表明MLN2704在一种新的成骨性前列腺癌转移模型中具有活性。