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使用MPDL3280A抑制程序性死亡受体1配体1(PD-L1)治疗实体瘤。

PD-L1 inhibition with MPDL3280A for solid tumors.

作者信息

Cha Edward, Wallin Jeffrey, Kowanetz Marcin

机构信息

Product Development Oncology, Genentech, Inc, South San Francisco, CA.

Oncology Biomarker Development, Genentech, Inc, South San Francisco, CA.

出版信息

Semin Oncol. 2015 Jun;42(3):484-7. doi: 10.1053/j.seminoncol.2015.02.002. Epub 2015 Feb 12.

Abstract

Cancer immunotherapy has become a popular anticancer approach, with the goal of stimulating immune responses against tumor cells. Recent evidence has demonstrated that the use of monoclonal antibodies targeting the programmed death ligand-1 (PD-L1)/programmed death-1 (PD-1) checkpoint pathway can result in well-tolerated clinical responses in a wide variety of tumor types. This review summarizes the safety, clinical activity and biomarker data for the anti-PD-L1 antibody, MPDL3280A, from a phase Ia multicenter, dose-escalation and -expansion trial. The data to date suggest that MPDL3280A is most effective in patients with pre-existing immunity suppressed by PD-L1 and reinvigorated upon antibody treatment.

摘要

癌症免疫疗法已成为一种流行的抗癌方法,其目标是激发针对肿瘤细胞的免疫反应。最近的证据表明,使用靶向程序性死亡配体-1(PD-L1)/程序性死亡-1(PD-1)检查点通路的单克隆抗体可在多种肿瘤类型中产生耐受性良好的临床反应。本综述总结了来自一项Ia期多中心、剂量递增和扩展试验的抗PD-L1抗体MPDL3280A的安全性、临床活性和生物标志物数据。迄今为止的数据表明,MPDL3280A在那些预先存在的免疫被PD-L1抑制且在抗体治疗后恢复活力的患者中最为有效。

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