Literature DB >> 25965366

PD-L1 blockade for cancer treatment: MEDI4736.

Ramy Ibrahim1, Ross Stewart2, Aiman Shalabi3.   

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.
Copyright © 2015 Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 25965366     DOI: 10.1053/j.seminoncol.2015.02.007

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  39 in total

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Review 2.  Assessment of the PD-L1 status by immunohistochemistry: challenges and perspectives for therapeutic strategies in lung cancer patients.

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4.  Tumor vaccines and cellular immunotherapies.

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5.  Durvalumab after chemoradiotherapy in stage III non-small cell lung cancer.

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Review 6.  Novel cancer antigens for personalized immunotherapies: latest evidence and clinical potential.

Authors:  Gregory T Wurz; Chiao-Jung Kao; Michael W DeGregorio
Journal:  Ther Adv Med Oncol       Date:  2016-01       Impact factor: 8.168

7.  Emerging immunotherapeutics in adenocarcinomas: A focus on CAR-T cells.

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Review 8.  Brain-immune interactions in perinatal hypoxic-ischemic brain injury.

Authors:  Bo Li; Katherine Concepcion; Xianmei Meng; Lubo Zhang
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Review 9.  Immune checkpoint blockade in human cancer therapy: lung cancer and hematologic malignancies.

Authors:  Murali Janakiram; Vipul Pareek; Haiying Cheng; Deepa M Narasimhulu; Xingxing Zang
Journal:  Immunotherapy       Date:  2016-06       Impact factor: 4.196

10.  PD-L1 Monoclonal Antibody Treats Ischemic Stroke by Controlling Central Nervous System Inflammation.

Authors:  Sheetal Bodhankar; Yingxin Chen; Andrew Lapato; Abby L Dotson; Jianming Wang; Arthur A Vandenbark; Julie A Saugstad; Halina Offner
Journal:  Stroke       Date:  2015-08-25       Impact factor: 7.914

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