Biomarkers in drug development: friend or foe? A personal reflection gained working within oncology

被引:11
作者
Carroll, Kevin J. [1 ]
机构
[1] AstraZeneca Pharm, Global Clin Funct, Macclesfield, Cheshire, England
关键词
biomarkers; surgery; prognostic; predictive; oncology;
D O I
10.1002/pst.269
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hopes and expectations for the use and utility of new, emerging biomarkers in drug development have probably never been higher, especially in oncology. Biomarkers are exalted as vital patient selection tools in an effort to target those most likely to benefit from a new drug, and so to reduce development costs, lessen risk and expedite developments times. It is further hoped that biomarkers can be used as surrogate endpoints for clinical outcomes, to demonstrate effectiveness and, ultimately, to support drug approval. However, I perceive that all is not straightforward, and, particularly in terms of the promise of accelerated drug development, biomarker strategies may not in all cases deliver the advances and advantages hoped for. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:253 / 260
页数:8
相关论文
共 16 条
[1]   VALUE OF A RUN-IN PERIOD IN A DRUG TRIAL DURING PREGNANCY [J].
BLACKWELDER, WC ;
HASTINGS, BK ;
LEE, MLF ;
DELORIA, MA .
CONTROLLED CLINICAL TRIALS, 1990, 11 (03) :187-198
[2]   THE RUN-IN PERIOD IN CLINICAL-TRIALS - THE EFFECT OF MISCLASSIFICATION ON EFFICIENCY [J].
BRITTAIN, E ;
WITTES, J .
CONTROLLED CLINICAL TRIALS, 1990, 11 (05) :327-338
[3]   Criteria for the validation of surrogate endpoints in randomized experiments [J].
Buyse, M ;
Molenberghs, G .
BIOMETRICS, 1998, 54 (03) :1014-1029
[4]  
BUYSE M, 2005, J CLIN ONCOLOGY 1, V23
[5]   Is prostate-specific antigen a valid surrogate end point for survival in hormonally treated patients with metastatic prostate cancer?: Joint research of the European Organisation for Research and Treatment of Cancer, the Limburgs Universitair Centrum, and AstraZeneca Pharmaceuticals [J].
Collette, L ;
Burzykowski, T ;
Carroll, KJ ;
Newling, D ;
Morris, T ;
Schröder, FH .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :6139-6148
[6]   Considerations in the evaluation of surrogate endpoints in clinical trials: Summary of a National Institutes of Health Workshop [J].
De Gruttola, VG ;
Clax, P ;
DeMets, DL ;
Downing, GJ ;
Ellenberg, SS ;
Friedman, L ;
Gail, MH ;
Prentice, R ;
Wittes, J ;
Zeger, SL .
CONTROLLED CLINICAL TRIALS, 2001, 22 (05) :485-502
[7]   Mutations in the epidermal growth factor receptor and in KRAS are predictive and prognostic indicators in patients with non-small-cell lung cancer treated with chemotherapy alone and in combination with erlotinib [J].
Eberhard, DA ;
Johnson, BE ;
Amler, LC ;
Goddard, AD ;
Heldens, SL ;
Herbst, RS ;
Ince, WL ;
Jänne, PA ;
Januario, T ;
Johnson, DH ;
Klein, P ;
Miller, VA ;
Ostland, MA ;
Ramies, DA ;
Sebisanovic, D ;
Stinson, JA ;
Zhang, YR ;
Seshagiri, S ;
Hillan, KJ .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :5900-5909
[8]  
*FDA, 2004, FDA PUBL WORKSH CLIN
[9]   STATISTICAL VALIDATION OF INTERMEDIATE END-POINTS FOR CHRONIC DISEASES [J].
FREEDMAN, LS ;
GRAUBARD, BI ;
SCHATZKIN, A .
STATISTICS IN MEDICINE, 1992, 11 (02) :167-178
[10]   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