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用于癌症治疗的程序性死亡受体 1 配体(PD-L1)阻断:MEDI4736。

PD-L1 blockade for cancer treatment: MEDI4736.

作者信息

Ibrahim Ramy, Stewart Ross, Shalabi Aiman

机构信息

AstraZeneca Immuno-Oncology, Gaithersburg, MD.

MedImmune Ltd, Cambridge, UK.

出版信息

Semin Oncol. 2015 Jun;42(3):474-83. doi: 10.1053/j.seminoncol.2015.02.007. Epub 2015 Feb 25.

Abstract

MEDI4736 is a human immunoglobulin (Ig) G1к monoclonal antibody that blocks programmed cell death ligand-1 (PD-L1) binding to its receptors, allowing T cells to recognize and kill tumor cells. Key attributes include high affinity and selectivity for PD-L1, sustained drug exposure for up to 1 year of dosing, and engineering of the antibody to prevent antibody-dependent cell-mediated cytotoxicity. No immunogenicity impacting on the pharmacokinetics/pharmacodynamics of MEDI4736 has been reported at the 10 mg/kg every 2 weeks dose selected for further clinical development. The current safety profile and encouraging early anti-tumor activity of MEDI4736 support further clinical assessment. A broad development program for MEDI4736, both as monotherapy and in combination, is underway across a range of tumor types. This includes a large, multicenter, phase I, dose-escalation/expansion study in solid tumors (with a smaller corresponding study in Japanese patients), a phase I study in myelodysplastic syndrome, and a phase II study in advanced colorectal cancer. In addition, multiple phase I combination studies are ongoing with different agents, including those targeting MEK/BRAF in melanoma, epidermal growth factor receptor, programmed cell death-1, cytotoxic T-lymphocyte antigen-4, OX40, chemokine (C-C motif) receptor 4, and indoleamine 2,3-dioxygenase. Development is most advanced in non-small cell lung cancer, with a program currently comprising four pivotal studies and three phase I combination studies. A pivotal program for MEDI4736 in head and neck cancer began in late 2014.

摘要

MEDI4736是一种人免疫球蛋白(Ig)G1к单克隆抗体,可阻断程序性细胞死亡配体-1(PD-L1)与其受体的结合,使T细胞能够识别并杀死肿瘤细胞。关键特性包括对PD-L1具有高亲和力和选择性、长达1年给药期的持续药物暴露,以及对抗体进行改造以防止抗体依赖性细胞介导的细胞毒性。在为进一步临床开发选定的每2周10 mg/kg剂量下,尚未有影响MEDI4736药代动力学/药效学的免疫原性报告。MEDI4736目前的安全性概况和令人鼓舞的早期抗肿瘤活性支持进一步的临床评估。针对MEDI4736的广泛开发计划正在进行,包括单药治疗和联合治疗,涉及多种肿瘤类型。这包括一项针对实体瘤的大型多中心I期剂量递增/扩展研究(在日本患者中有一项规模较小的相应研究)、一项针对骨髓增生异常综合征的I期研究,以及一项针对晚期结直肠癌的II期研究。此外,正在开展多项与不同药物的I期联合研究,包括针对黑色素瘤中MEK/BRAF、表皮生长因子受体、程序性细胞死亡-1、细胞毒性T淋巴细胞抗原-4、OX40、趋化因子(C-C基序)受体4和吲哚胺2,3-双加氧酶的药物。在非小细胞肺癌中的开发进展最为显著,目前该计划包括四项关键研究和三项I期联合研究。MEDI4736针对头颈癌的关键计划于2014年末启动。

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