首页> 外文期刊>Expert opinion on biological therapy >Tremelimumab (CP-675,206): a fully human anticytotoxic T lymphocyte-associated antigen 4 monoclonal antibody for treatment of patients with advanced cancers.
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Tremelimumab (CP-675,206): a fully human anticytotoxic T lymphocyte-associated antigen 4 monoclonal antibody for treatment of patients with advanced cancers.

机译:Tremelimumab(CP-675,206):一种用于治疗晚期癌症的完全人抗细胞毒性T淋巴细胞相关抗原4单克隆抗体。

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摘要

Tremelimumab, a fully human monoclonal IgG2 antibody targeting cytotoxic T lymphocyte-associated antigen 4 (CTLA4), is being developed by Pfizer for treatment of patients with advanced cancers. Treatment with an anti-CTLA4 mAb prevents normal downregulation of T cells and prolongs T cell activation, thereby enhancing immune function. In Phase I and II studies, tremelimumab was well tolerated with predictable and manageable side effects. Antitumor activity with monotherapy was observed in patients with advanced melanoma and colorectal cancer (objective response rates of approximately 10 and 2%, respectively), and most objective responses were durable (defined as lasting > 180 days). Additional Phase II and III studies in combination with other agents will assess antitumor activity in multiple tumor types as well as attempt to identify patient populations most likely to respond.
机译:辉瑞公司正在开发针对细胞毒性T淋巴细胞相关抗原4(CTLA4)的全人类单克隆IgG2抗体Tremelimumab,该药物可用于治疗晚期癌症患者。抗CTLA4 mAb的治疗可防止T细胞正常下调并延长T细胞活化,从而增强免疫功能。在I和II期研究中,tremelimumab具有可预测和可控制的副作用,耐受性良好。在晚期黑素瘤和结直肠癌患者中观察到单药治疗的抗肿瘤活性(客观缓解率分别约为10%和2%),并且大多数客观缓解是持久的(定义为持续> 180天)。与其他药物联合进行的其他II和III期研究将评估多种肿瘤类型的抗肿瘤活性,并尝试确定最有可能做出反应的患者人群。

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