Methodology and limits of preclinical evaluation during the development of anticancer drug combinations

被引:0
|
作者
Vassal, G
机构
[1] Inst Gustave Roussy, Dept Pediat, F-94805 Villejuif, France
[2] Inst Gustave Roussy, Lab Pharmacotoxicol & Pharmacogenet, CNRS, UMR 1772, F-94805 Villejuif, France
关键词
synergism; additivity; antagonism;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In chemosensitive tumors, cancer chemotherapy is active as drug combinations. During the development of new anticancer drugs, preclinical experimental models may help to design drug combinations. Indeed, in vitro models are able to define drug interactions in terms of synergism, additivity or antagonism, while in vivo models can evaluate therapeutic synergism along with toxicity in a clinical setting. The methodology for in vitro and in vivo evaluation of anticancer drug combinations is described. The limits are discussed. In conclusion, preclinical models contribute to the clinical therapeutic principles.
引用
收藏
页码:929 / 934
页数:6
相关论文
共 50 条
  • [31] Chemotherapeutic Drug Delivery Nanoplatform Development: From Physicochemical to Preclinical Evaluation
    Kontogiannis, Orestis
    Selianitis, Dimitrios
    Palikaras, Konstantinos
    Pippa, Natassa
    Pispas, Stergios
    Efstathopoulos, Efstathios
    Gazouli, Maria
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (21)
  • [32] Preclinical and clinical drug development
    Henry, Brian
    IDRUGS, 2007, 10 (02) : 106 - 108
  • [33] A Physiologically Based Modeling Strategy during Preclinical CNS Drug Development
    Ball, Kathryn
    Bouzom, Francois
    Scherrmann, Jean-Michel
    Walther, Bernard
    Decleves, Xavier
    MOLECULAR PHARMACEUTICS, 2014, 11 (03) : 836 - 848
  • [34] GASTROSCOPY IN THE CONSCIOUS DOG DURING TOXICOLOGICAL STUDIES IN PRECLINICAL DRUG DEVELOPMENT
    SCHMITT, PJ
    LABORATORY ANIMAL SCIENCE, 1987, 37 (04): : 521 - 522
  • [35] Evaluation of drug risk during pregnancy: methodology and risk management
    Elefant, E
    SainteCroix, A
    THERAPIE, 1997, 52 (04): : 307 - 312
  • [36] Cytotoxicity of TRAIL/anticancer drug combinations in human normal cells
    Meurette, Olivier
    Fontaine, Anne
    Rebillard, Amelie
    Le Moigne, Gwenaelle
    Lamy, Thierry
    Lagadic-Gossmann, Dominique
    Dimanche-Boitrel, Marie-Therese
    SIGNAL TRANSDUCTION PATHWAYS, PT A: APOPTOTIC AND EXTRACELLULAR SIGNALING, 2006, 1090 : 209 - 216
  • [37] drugCARD: a database of anticancer treatment regimens and drug combinations.
    Fernandez, Eric
    Pang, Jianxiong
    Snell, Chris
    Derow, Cathy
    Brightman, Frances
    Chassagnoie, Christophe
    Jackson, Robert
    CANCER RESEARCH, 2013, 73 (08)
  • [38] Deep graph embedding for prioritizing synergistic anticancer drug combinations
    Jiang, Peiran
    Huang, Shujun
    Fu, Zhenyuan
    Sun, Zexuan
    Lakowski, Ted M.
    Hu, Pingzhao
    COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, 2020, 18 : 427 - 438
  • [39] Enhancing anticancer activity of macrophages through rational drug combinations
    Mills, Gordon B.
    Labrie, Marilyne
    JOURNAL OF CLINICAL INVESTIGATION, 2024, 134 (09):
  • [40] Medicoeconomic evaluation: aims, methodology, limits
    Daures, JP
    Delande, G
    GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE, 2000, 24 (11): : 1029 - 1031