Department of Medicine, Roswell Park Cancer Institute, Elm & Carlton Streets, Buffalo, NY 14263, USA.
Future Oncol. 2011 Aug;7(8):963-79. doi: 10.2217/fon.11.79.
The year 1997 was pivotal in lymphoma research, as it was the year that the US FDA approved rituximab. Rituximab significantly altered clinical management and outcomes of patients with B-cell malignancies. Despite a high initial response rate, the majority of patients subsequently develop variable degrees of therapeutic resistance to rituximab. Research attempting to understand the mechanisms of rituximab resistance and potential ways to overcome them has given rise to the development of novel targeted immunotherapeutics. This article will update the readers on advances in bioengineering of monoclonal antibodies and immunoconjugates that target CD20, as well as other surface antigens. Some additional novel immunotherapeutics, including small modular immunopharmaceuticals, bispecific monoclonal antibodies, T-cell engaging antibodies and immunoconjugates, will also be discussed.
1997 年是淋巴瘤研究的关键一年,因为这一年美国 FDA 批准了利妥昔单抗。利妥昔单抗显著改变了 B 细胞恶性肿瘤患者的临床管理和预后。尽管初始反应率很高,但大多数患者随后对利妥昔单抗产生不同程度的治疗耐药性。为了了解利妥昔单抗耐药的机制和潜在的克服方法的研究,催生了新型靶向免疫治疗药物的发展。本文将为读者提供有关靶向 CD20 的单克隆抗体和免疫偶联物的生物工程学方面的最新进展,以及其他表面抗原的相关信息。本文还将讨论一些其他新型免疫治疗药物,包括小分子模块化免疫药物、双特异性单克隆抗体、T 细胞衔接抗体和免疫偶联物。