Ponte Jose F, Ab Olga, Lanieri Leanne, Lee Jenny, Coccia Jennifer, Bartle Laura M, Themeles Marian, Zhou Yinghui, Pinkas Jan, Ruiz-Soto Rodrigo
ImmunoGen, Inc., Waltham, MA, USA.
ImmunoGen, Inc., Waltham, MA, USA.
Neoplasia. 2016 Dec;18(12):775-784. doi: 10.1016/j.neo.2016.11.002. Epub 2016 Nov 25.
Elevated folate receptor alpha (FRα) expression is characteristic of epithelial ovarian cancer (EOC), thus establishing this receptor as a candidate target for the development of novel therapeutics to treat this disease. Mirvetuximab soravtansine (IMGN853) is an antibody-drug conjugate (ADC) that targets FRα for tumor-directed delivery of the maytansinoid DM4, a potent agent that induces mitotic arrest by suppressing microtubule dynamics. Here, combinations of IMGN853 with approved therapeutics were evaluated in preclinical models of EOC. Combinations of IMGN853 with carboplatin or doxorubicin resulted in synergistic antiproliferative effects in the IGROV-1 ovarian cancer cell line in vitro. IMGN853 potentiated the cytotoxic activity of carboplatin via growth arrest and augmented DNA damage; cell cycle perturbations were also observed in cells treated with the IMGN853/doxorubicin combination. These benefits translated into improved antitumor activity in patient-derived xenograft models in vivo in both the platinum-sensitive (IMGN853/carboplatin) and platinum-resistant (IMGN853/pegylated liposomal doxorubicin) settings. IMGN853 co-treatment also improved the in vivo efficacy of bevacizumab in platinum-resistant EOC models, with combination regimens causing significant regressions and complete responses in the majority of tumor-bearing mice. Histological analysis of OV-90 ovarian xenograft tumors revealed that concurrent administration of IMGN853 and bevacizumab caused rapid disruption of tumor microvasculature and extensive necrosis, underscoring the superior bioactivity profile of the combination regimen. Overall, these demonstrations of combinatorial benefit conferred by the addition of the first FRα-targeting ADC to established therapies provide a compelling framework for the potential application of IMGN853 in the treatment of patients with advanced ovarian cancer.
叶酸受体α(FRα)表达升高是上皮性卵巢癌(EOC)的特征,因此将该受体确立为开发治疗该疾病新疗法的候选靶点。Mirvetuximab soravtansine(IMGN853)是一种抗体药物偶联物(ADC),靶向FRα以实现对肿瘤的靶向递送美登素DM4,这是一种通过抑制微管动力学诱导有丝分裂停滞的强效药物。在此,在EOC的临床前模型中评估了IMGN853与已批准疗法的联合应用。IMGN853与卡铂或多柔比星联合在体外IGROV-1卵巢癌细胞系中产生协同抗增殖作用。IMGN853通过生长停滞增强卡铂的细胞毒活性并增加DNA损伤;在用IMGN853/多柔比星联合治疗的细胞中也观察到细胞周期紊乱。这些益处转化为在体内铂敏感(IMGN853/卡铂)和铂耐药(IMGN853/聚乙二醇化脂质体多柔比星)环境下患者来源的异种移植模型中抗肿瘤活性的提高。IMGN853联合治疗还提高了贝伐单抗在铂耐药EOC模型中的体内疗效,联合方案在大多数荷瘤小鼠中导致显著的肿瘤消退和完全缓解。对OV-90卵巢异种移植肿瘤的组织学分析表明,同时给予IMGN853和贝伐单抗会导致肿瘤微血管迅速破坏和广泛坏死,突出了联合方案优越的生物活性特征。总体而言,将首个靶向FRα的ADC添加到既定疗法中所带来的联合益处的这些证明为IMGN853在晚期卵巢癌患者治疗中的潜在应用提供了令人信服的框架。