Maloney D G, Press O W
Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Oncology (Williston Park). 1998 Oct;12(10 Suppl 8):63-76.
Significant advances have been made in the application of monoclonal antibody-based therapies to the treatment of patients with lymphoma. The most promising areas appear to be the use of unconjugated monoclonal antibodies and the use of radiolabeled monoclonal antibodies. The recent approval by the US Food and Drug Administration (FDA) of rituximab (Rituxan), an unconjugated chimeric antibody against the CD20 antigen for the treatment of relapsed low-grade or follicular B-cell non-Hodgkin's lymphoma marked a milestone in the development of these antibody-based treatments. Other new drug applications to the FDA are pending using both unconjugated and radiolabeled monoclonal antibodies, and it is anticipated that further new treatment options based on monoclonal antibody technology will soon be available for the treatment of patients with non-Hodgkin's lymphoma. Forthcoming clinical trial results combining these new agents with current therapies are needed to determine if the addition of these new biologic agents to our armamentarium against lymphoma will alter the natural history of this disease for our patients. The most promising of these treatments and the comparison of these strategies are reviewed here.
基于单克隆抗体的疗法在淋巴瘤患者治疗中的应用已取得显著进展。最有前景的领域似乎是未偶联单克隆抗体的使用和放射性标记单克隆抗体的使用。美国食品药品监督管理局(FDA)最近批准了利妥昔单抗(美罗华),一种针对CD20抗原的未偶联嵌合抗体,用于治疗复发的低度或滤泡性B细胞非霍奇金淋巴瘤,这标志着这些基于抗体的治疗方法发展中的一个里程碑。其他使用未偶联和放射性标记单克隆抗体的新药申请正在等待FDA审批,预计基于单克隆抗体技术的更多新治疗选择很快将可用于非霍奇金淋巴瘤患者的治疗。需要即将开展的将这些新药与现有疗法相结合的临床试验结果,以确定在我们对抗淋巴瘤的武器库中添加这些新生物制剂是否会改变我们患者的这种疾病的自然病程。本文将对这些最有前景的治疗方法以及这些策略的比较进行综述。