Clinical and economic impact of the nonresponder phenomenon - implications for systems based discovery

被引:7
作者
Jackson, David B. [1 ]
机构
[1] LIFE Biosyst GmbH, D-69115 Heidelberg, Germany
关键词
IMATINIB; THERAPY; CANCER;
D O I
10.1016/j.drudis.2009.01.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Molecular diversity is a hallmark of life. Unfortunately, given that the clinical benefit of a drug can only be realized under certain genetic/molecular conditions, such heterogeneity can mean the difference between survival and death. For most targeted therapies it appears that such conditions are met in only a small percentage of patients, particularly in the monotherapy context. Notwithstanding, the nonresponder phenomenon can be viewed as a low-hanging fruit among medical needs, with a large body of scientific knowledge surrounding the target and the diseased system. This knowledge, together with information about the molecular sources of nonresponse, provides a rational framework upon which novel intervention strategies can be built. Driven by such molecular considerations and the enormous economic implications, new levels of innovation are urgently required. Systems level patient characterization coupled with innovative in silico strategies hold great promise and suggest a future of theranostic-linked combination therapies, optimized cohort selection and rational prioritization of clinical opportunities.
引用
收藏
页码:380 / 385
页数:6
相关论文
共 8 条
[1]   The biology of chronic myelogenous leukemia: Implications for imatinib therapy [J].
Alvarez, Ricardo H. ;
Kantarjian, Hagop ;
Cortes, Jorge E. .
SEMINARS IN HEMATOLOGY, 2007, 44 (01) :S4-S14
[2]   Therapeutic drug monitoring in CML patients on imatinib [J].
Blasdel, Carolyn ;
Egorin, Merrill J. ;
Lagattuta, Theodore F. ;
Druker, Brian J. ;
Deininger, Michael W. .
BLOOD, 2007, 110 (05) :1699-1701
[3]  
Karatsuba A., 1963, Sov. Phys. Doklady, V7, P595
[4]   KRAS mutation status is predictive of response to cetuximab therapy in colorectal cancer [J].
Lièvre, A ;
Bachet, JB ;
Le Corre, D ;
Boige, V ;
Landi, B ;
Emile, JF ;
Côté, JF ;
Tomasic, G ;
Penna, C ;
Ducreux, M ;
Rougier, P ;
Penault-Llorca, F ;
Laurent-Puig, P .
CANCER RESEARCH, 2006, 66 (08) :3992-3995
[5]   Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib [J].
Lynch, TJ ;
Bell, DW ;
Sordella, R ;
Gurubhagavatula, S ;
Okimoto, RA ;
Brannigan, BW ;
Harris, PL ;
Haserlat, SM ;
Supko, JG ;
Haluska, FG ;
Louis, DN ;
Christiani, DC ;
Settleman, J ;
Haber, DA .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (21) :2129-2139
[6]  
Poincare H., 1902, Science and Hypothesis
[7]   The second generation of BCR-ABL tyrosine kinase inhibitors [J].
Tauchi, Tetsuzo ;
Ohyashiki, Kazuma .
INTERNATIONAL JOURNAL OF HEMATOLOGY, 2006, 83 (04) :294-300
[8]  
*WORLD BEST SELL M, 2007, MEDADNEWS