Novel immune check point inhibiting antibodies in cancer therapy-Opportunities and challenges

被引:85
作者
Diesendruck, Yael [1 ]
Benhar, Itai [1 ]
机构
[1] Tel Aviv Univ, George S Wise Fac Life Sci, Dept Mol Microbiol & Biotechnol, IL-69978 Tel Aviv, Israel
关键词
Immune checkpoint inhibitors; Therapeutic monoclonal antibodies; CTLA4; PD-1-PDL-1; axis; Immune-related adverse events; CELL LUNG-CANCER; LYMPHOCYTE-ACTIVATION GENE-3; ADVANCED MELANOMA; DOUBLE-BLIND; MULTIDRUG-RESISTANCE; DRUG-RESISTANCE; ADVERSE EVENTS; MALIGNANT-MELANOMA; ANTITUMOR-ACTIVITY; CLINICAL ACTIVITY;
D O I
10.1016/j.drup.2017.02.001
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Drug resistance of tumor cells to chemotherapy is limiting the therapeutic efficacy of most anticancer drugs and represents a major obstacle in medical oncology. However, treatment of various human malignancies with biologics, mostly monoclonal antibodies (mAbs), is not limited by such chemoresistance mechanisms. However, other resistance or evasion mechanisms limit the efficacy to anticancer therapeutic mAbs that engage tumor-associated antigens on the surface of the malignant cells. Immune checkpoint blocking monoclonal antibodies are heralded as a promising therapeutic approach in clinical oncology. These mAbs do not directly attack the malignant cells as most anticancer mAbs; rather, they enhance the anti-tumor response of the immune system by targeting immune regulatory pathways. Three mAbs targeting immune checkpoint molecules are currently used in the clinic and new mAbs that target other potential inhibitory targets are being actively investigated. This therapeutic approach, while proving as highly beneficial for many patients, is prone to toxicities and side effects of an autoimmune nature. Defining suitable management algorithms and biomarkers that predict therapeutic effects and adverse toxicity are required to provide survival benefit for larger numbers of cancer patients. Overcoming these challenges, along with opportunities for new agents and combinatorial strategies are the main focus of immune checkpoint blockade research today. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:39 / 47
页数:9
相关论文
共 121 条
[2]
PD-1 Blockade with Nivolumab in Relapsed or Refractory Hodgkin's Lymphoma [J].
Ansell, Stephen M. ;
Lesokhin, Alexander M. ;
Borrello, Ivan ;
Halwani, Ahmad ;
Scott, Emma C. ;
Gutierrez, Martin ;
Schuster, Stephen J. ;
Millenson, Michael M. ;
Cattry, Deepika ;
Freeman, Gordon J. ;
Rodig, Scott J. ;
Chapuy, Bjoern ;
Ligon, Azra H. ;
Zhu, Lili ;
Grosso, Joseph F. ;
Kim, Su Young ;
Timmerman, John M. ;
Shipp, Margaret A. ;
Armand, Philippe .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (04) :311-319
[3]
CD39 and CD73 in immunity and inflammation [J].
Antonioli, Luca ;
Pacher, Pal ;
Vizi, E. Sylvester ;
Hasko, Gyoergy .
TRENDS IN MOLECULAR MEDICINE, 2013, 19 (06) :355-367
[4]
Molecular basis of antifolate resistance [J].
Assaraf, Yehuda G. .
CANCER AND METASTASIS REVIEWS, 2007, 26 (01) :153-181
[5]
The role of multidrug resistance efflux transporters in antifolate resistance and folate homeostasis [J].
Assaraf, Yehuda G. .
DRUG RESISTANCE UPDATES, 2006, 9 (4-5) :227-246
[6]
Autoimmunity correlates with tumor regression in patients with metastatic melanoma treated with anti-cytotoxic T-lymphocyte antigen-4 [J].
Attia, P ;
Phan, GQ ;
Maker, AV ;
Robinson, MR ;
Quezado, MM ;
Yang, JC ;
Sherry, RM ;
Topalian, SL ;
Kammula, US ;
Royal, RE ;
Restifo, NP ;
Haworth, LR ;
Levy, C ;
Mavroukakis, SA ;
Nichol, G ;
Yellin, MJ ;
Rosenberg, SA .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :6043-6053
[7]
Phase I Study of Single-Agent Anti-Programmed Death-1 (MDX-1106) in Refractory Solid Tumors: Safety, Clinical Activity, Pharmacodynamics, and Immunologic Correlates [J].
Brahmer, Julie R. ;
Drake, Charles G. ;
Wollner, Ira ;
Powderly, John D. ;
Picus, Joel ;
Sharfman, William H. ;
Stankevich, Elizabeth ;
Pons, Alice ;
Salay, Theresa M. ;
McMiller, Tracee L. ;
Gilson, Marta M. ;
Wang, Changyu ;
Selby, Mark ;
Taube, Janis M. ;
Anders, Robert ;
Chen, Lieping ;
Korman, Alan J. ;
Pardoll, Drew M. ;
Lowy, Israel ;
Topalian, Suzanne L. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (19) :3167-3175
[8]
Pidilizumab in the treatment of diffuse large B-cell lymphoma [J].
Bryan, Locke J. ;
Gordon, Leo I. .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2014, 14 (09) :1361-1368
[9]
CTLA-4-mediated inhibition in regulation of T cell responses: Mechanisms and manipulation in tumor immunotherapy [J].
Chambers, CA ;
Kuhns, MS ;
Egen, JG ;
Allison, JP .
ANNUAL REVIEW OF IMMUNOLOGY, 2001, 19 :565-594
[10]
Tremelimumab: research and clinical development [J].
Comin-Anduix, Begona ;
Escuin-Ordinas, Helena ;
Ibarrondo, Francisco Javier .
ONCOTARGETS AND THERAPY, 2016, 9 :1767-1776