McLaughlin P, White C A, Grillo-López A J, Maloney D G
Department of Lymphoma and Myeloma, UT M. D. Anderson Cancer Center, Houston, Texas, USA.
Oncology (Williston Park). 1998 Dec;12(12):1763-9; discussion 1769-70, 1775-7,.
Rituximab (IDEC-C2B8 [Rituxan]) is a chimeric anti-CD20 monoclonal antibody (MoAb) that was recently approved by the FDA for the treatment of patients with low-grade or follicular B-cell non-Hodgkin's lymphoma. Its potential efficacy in other B-cell malignancies is currently being explored. This article reviews the mechanisms of action of rituximab, as well as preclinical data and results of the clinical trials that led to its approval. Also discussed are the mechanics of administering rituximab on the recommended weekly x 4 outpatient schedule. Finally, the article describes ongoing and planned trials of rituximab in other dosage schedules, in other B-cell neoplasms, and in conjunction with chemotherapy. As the first MoAb to gain FDA approval for the treatment of a malignancy, rituximab signals the beginning of a promising new era in cancer therapy.
利妥昔单抗(IDEC-C2B8 [美罗华])是一种嵌合型抗CD20单克隆抗体(MoAb),最近被美国食品药品监督管理局(FDA)批准用于治疗低度或滤泡性B细胞非霍奇金淋巴瘤患者。目前正在探索其在其他B细胞恶性肿瘤中的潜在疗效。本文回顾了利妥昔单抗的作用机制,以及导致其获批的临床前数据和临床试验结果。还讨论了按照推荐的每周一次、共4次的门诊给药方案使用利妥昔单抗的具体方法。最后,本文描述了利妥昔单抗在其他给药方案、其他B细胞肿瘤以及与化疗联合使用方面正在进行和计划开展的试验。作为首个获得FDA批准用于治疗恶性肿瘤的单克隆抗体,利妥昔单抗标志着癌症治疗一个充满希望的新时代的开始。