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奥法妥珠单抗,一种新型抗 CD20 单克隆抗体,用于治疗 B 细胞恶性肿瘤。

Ofatumumab, a novel anti-CD20 monoclonal antibody for the treatment of B-cell malignancies.

机构信息

Georgetown University Hospital, Lombardi Comprehensive Cancer Center, 3800 Reservoir Rd NW, Washington, DC 20007, USA.

出版信息

J Clin Oncol. 2010 Jul 20;28(21):3525-30. doi: 10.1200/JCO.2010.27.9836. Epub 2010 May 10.

Abstract

The availability of safe and effective monoclonal antibodies (mAbs) has dramatically altered treatment strategies for B-cell malignancies. Rituximab, a type I chimeric anti-CD20 mAb, not only has activity against a broad range of CD20-positive B-cell malignancies but also, when combined with chemotherapy or other biologic agents, has improved response rates; in addition, in certain situations, progression-free survival and even overall survival may be prolonged. Recently, other anti-CD20 mAbs have been developed to improve on the activity achieved with rituximab or to demonstrate efficacy in patients whose diseases are resistant to rituximab. The most extensively studied of these is ofatumumab, a type I human antibody that binds to a different epitope of CD20 than rituximab. Preclinical data suggest improved complement-dependent cytotoxicity and antibody-dependent cellular cytotoxicity compared with rituximab. In early clinical trials, ofatumumab demonstrated single-agent activity against chronic lymphocytic leukemia (CLL) and a number of histologies of B-cell non-Hodgkin's lymphomas. This antibody was recently approved by the US Food and Drug Administration for the treatment of CLL that is resistant to both fludarabine and alemtuzumab. Additional study is ongoing with ofatumumab in combination with chemotherapy and biologic agents to further enhance its efficacy. Ofatumumab offers another effective agent with which to improve the outcome of patients with B-cell malignancies.

摘要

安全有效的单克隆抗体(mAbs)的出现极大地改变了 B 细胞恶性肿瘤的治疗策略。利妥昔单抗是一种 I 型嵌合抗 CD20 mAb,不仅对广泛的 CD20 阳性 B 细胞恶性肿瘤具有活性,而且与化疗或其他生物制剂联合使用时可提高反应率;此外,在某些情况下,无进展生存期甚至总生存期可能会延长。最近,开发了其他抗 CD20 mAbs 以提高利妥昔单抗的活性,或在对利妥昔单抗耐药的患者中证明疗效。其中研究最多的是奥法妥珠单抗,这是一种 I 型人源抗体,与利妥昔单抗结合的 CD20 表位不同。临床前数据表明与利妥昔单抗相比,补体依赖性细胞毒性和抗体依赖性细胞毒性得到了改善。在早期临床试验中,奥法妥珠单抗在慢性淋巴细胞白血病(CLL)和多种 B 细胞非霍奇金淋巴瘤组织学中表现出单药活性。该抗体最近已获得美国食品和药物管理局批准,用于治疗对氟达拉滨和阿仑单抗均耐药的 CLL。正在进行奥法妥珠单抗与化疗和生物制剂联合使用的研究,以进一步提高其疗效。奥法妥珠单抗提供了另一种有效药物,可改善 B 细胞恶性肿瘤患者的预后。

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