ImmunoGen, Inc., Waltham, MA, USA.
MAbs. 2009 Nov-Dec;1(6):548-51. doi: 10.4161/mabs.1.6.10029. Epub 2009 Nov 9.
Despite recent advances in the treatment of multiple myeloma, new agents are still needed to improve the outcome for patients. The established success of monoclonal antibodies in the treatment of some cancers has promoted interest in developing antibody-based therapies for multiple myeloma. Efforts have included the development of antibodies conjugated to potent cytotoxic moieties that combine the specificity of anti-myeloma-targeting antibodies with highly active anti-tumor compounds. Two such immunoconjugates currently in clinical development are composed of antibodies that target cell surface proteins found on multiple myeloma cells, and are coupled to cytotoxic maytansinoids. IMGN901 targets the neural cell adhesion molecule, CD56, which is expressed on the majority of myeloma cells, as well as on other cancers, while BT062 targets CD138, a primary diagnostic marker for multiple myeloma. In this review, we discuss the preclinical and early clinical data for these two promising new antibody-based anti-myeloma agents.
尽管多发性骨髓瘤的治疗在最近取得了进展,但仍需要新的药物来改善患者的预后。单克隆抗体在某些癌症治疗中的成功确立,促使人们对开发用于多发性骨髓瘤的基于抗体的治疗方法产生了兴趣。为此进行了许多努力,包括开发与有效细胞毒性基团偶联的抗体,将针对骨髓瘤靶向抗体的特异性与高活性抗肿瘤化合物结合起来。目前正在临床开发的两种免疫偶联物由靶向多发性骨髓瘤细胞表面蛋白的抗体组成,并与细胞毒性美登素偶联。IMGN901 靶向神经细胞黏附分子 CD56,该分子在大多数骨髓瘤细胞以及其他癌症上表达,而 BT062 则靶向多发性骨髓瘤的主要诊断标志物 CD138。在这篇综述中,我们讨论了这两种有前途的新型基于抗体的抗骨髓瘤药物的临床前和早期临床数据。