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Rituxan: The First 20 Years

机译:Rituxan:头20年

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摘要

Rituximab (Rituxan) was the first chimeric monoclonal antibody approved by the Food and Drug Administration (FDA) and the first approved for the treatment of cancer. Since then, combination therapy with various chemotherapeutic agents has increased response rates in lymphoma to almost 100% and has resulted in many cures. After its approval in 1997 for "relapsed or refractory, B-cell, low-grade, or follicular non-Hodgkin's lymphoma," Rituxan has subsequently been approved for other hematological indications as well as for use in several autoimmune diseases, including rheumatoid arthritis. Not only was Rituxan successful in treating lymphoma, but it also overcame the prevailing myth at that time, that monoclonal antibodies were not useful as therapeutics. It also opened the door for future development of many more monoclonal antibodies for treating cancer.
机译:利妥昔单抗(利特曲)是食品药品监督管理局(FDA)批准的第一个嵌合单克隆抗体,也是第一个批准用于治疗癌症的抗体。 从那时起,与各种化学治疗剂的联合疗法在淋巴瘤中的反应率提高到近100%,并导致了许多治疗方法。 在1997年批准“复发或耐火,B细胞,低度或卵泡非霍奇金淋巴瘤”之后,Rituxan随后被批准用于其他血液学适应症,以及在包括类风湿关节炎在内的几种自身免疫性疾病中使用。 Rituxan不仅成功地治疗了淋巴瘤,而且还克服了当时普遍存在的神话,单克隆抗体并不像疗法一样有用。 它还为未来开发更多用于治疗癌症的单克隆抗体开发了大门。

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