Baselga J, Norton L, Albanell J, Kim Y M, Mendelsohn J
Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Cancer Res. 1998 Jul 1;58(13):2825-31.
Recombinant humanized anti-HER2 antibody, rhuMAb HER2, inhibits the growth of breast cancer cells overexpressing HER2 and has clinical activity. We explored in preclinical models its capacity to enhance the tumoricidal effects of paclitaxel and doxorubicin. In cultures of naturally HER2-overexpressing cancer cells, rhuMAb HER2 inhibited growth and enhanced the cytotoxic effects of paclitaxel. Treatment of well established BT-474 breast cancer xenografts overexpressing HER2 in athymic mice with rhuMAb HER2 resulted in a dose-dependent antitumor activity. In combination studies, treatment with paclitaxel and rhuMAb HER2 or doxorubicin and rhuMAb HER2 resulted in greater inhibition of growth than that observed with any agent alone. The combination of paclitaxel and rhuMAb HER2 resulted in the highest tumor growth inhibition and had a significantly superior complete tumor regression rate when compared with either paclitaxel or rhuMAb HER2 alone. Clinical trials that are built on these results are under way.
重组人源化抗HER2抗体rhuMAb HER2可抑制过表达HER2的乳腺癌细胞生长,并具有临床活性。我们在临床前模型中探究了其增强紫杉醇和阿霉素杀瘤效果的能力。在天然过表达HER2的癌细胞培养物中,rhuMAb HER2可抑制生长并增强紫杉醇的细胞毒性作用。用rhuMAb HER2处理无胸腺小鼠体内已形成的过表达HER2的BT-474乳腺癌异种移植物,可产生剂量依赖性抗肿瘤活性。在联合研究中,与单独使用任何一种药物相比,紫杉醇与rhuMAb HER2联合治疗或阿霉素与rhuMAb HER2联合治疗对生长的抑制作用更强。紫杉醇与rhuMAb HER2联合使用导致最高的肿瘤生长抑制率,与单独使用紫杉醇或rhuMAb HER2相比,其完全肿瘤消退率显著更高。基于这些结果的临床试验正在进行中。