Application of biomarkers in the development of drugs intended for the treatment of osteoarthritis

被引:257
作者
Kraus, V. B. [1 ]
Burnett, B. [2 ]
Coindreau, J. [3 ]
Cottrell, S. [4 ]
Eyre, D. [5 ]
Gendreau, M. [6 ]
Gardiner, J. [7 ]
Garnero, P. [8 ,9 ,10 ,11 ]
Hardin, J. [12 ,13 ,14 ]
Henrotin, Y. [15 ]
Heinegard, D. [16 ]
Ko, A. [17 ]
Lohmander, L. S. [18 ]
Matthews, G. [19 ]
Menetski, J. [17 ]
Moskowitz, R. [20 ]
Persiani, S. [20 ,21 ]
Poole, A. R. [22 ]
Rousseau, J. -C. [9 ,10 ]
Todman, M. [23 ]
机构
[1] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[2] Duke Univ, Sch Med, Duke Translat Med Inst, Durham, NC 27710 USA
[3] Novartis Pharmaceut, E Hanover, NJ USA
[4] Amgen Inc, Seattle, WA USA
[5] Univ Washington, Dept Orthopaed & Sports Med, Seattle, WA 98195 USA
[6] Cypress Biosci Inc, San Diego, CA USA
[7] Wyeth Res, Discovery Translat Med, Collegeville, PA USA
[8] INSERM, UMR1033, F-69008 Lyon, France
[9] Univ Lyon, F-69008 Lyon, France
[10] Hosp Civils Lyon, Lyon, France
[11] Cis Bioassays, Codolet, France
[12] Albert Einstein Coll Med, Bronx, NY 10467 USA
[13] Montefiore Med Ctr, Bronx, NY 10467 USA
[14] Arthrit Fdn Natl Off, Atlanta, GA USA
[15] CHU Sart Tilman, Bone & Cartilage Res Unit, Inst Pathol, B-4000 Liege, Belgium
[16] Lund Univ, Dept Clin Sci, Rheumatol Sect, Lund, Sweden
[17] Merck & Co Inc, Rahway, NJ 07065 USA
[18] Lund Univ, Dept Orthopaed, Lund, Sweden
[19] Genzyme Corp, Cambridge, MA USA
[20] Case Western Reserve Univ, Univ Hosp, Cleveland, OH 44106 USA
[21] ROTTAPHARM MADAUS Monza, Dept Translat Sci & Pharmacokinet, Monza, Italy
[22] McGill Univ, Dept Surg, Montreal, PQ H3A 2T5, Canada
[23] Smith & Nephew Res Ctr, York, N Yorkshire, England
关键词
Osteoarthritis; Biomarkers; Clinical trial; OLIGOMERIC MATRIX PROTEIN; II COLLAGEN DEGRADATION; SURROGATE END-POINTS; OF-RHEUMATOLOGY CRITERIA; TOTAL-BODY BURDEN; KNEE OSTEOARTHRITIS; BIOCHEMICAL MARKERS; ARTICULAR-CARTILAGE; SYNOVIAL-FLUID; SERUM-LEVELS;
D O I
10.1016/j.joca.2010.08.019
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
Objective: Osteoarthritis (OA) is a chronic and slowly progressive disease for which biomarkers may be able to provide a more rapid indication of therapeutic responses to therapy than is currently available; this could accelerate and facilitate OA drug discovery and development programs. The goal of this document is to provide a summary and guide to the application of in vitro (biochemical and other soluble) biomarkers in the development of drugs for OA and to outline and stimulate a research agenda that will further this goal. Methods: The Biomarkers Working Group representing experts in the field of OA biomarker research from both academia and industry developed this consensus document between 2007 and 2009 at the behest of the Osteoarthritis Research Society International Federal Drug Administration initiative (OARSI FDA initiative). Results: This document summarizes definitions and classification systems for biomarkers, the current outcome measures used in OA clinical trials, applications and potential utility of biomarkers for development of OA therapeutics, the current state of qualification of OA-related biomarkers, pathways for biomarker qualification, critical needs to advance the use of biomarkers for drug development, recommendations regarding practices and clinical trials, and a research agenda to advance the science of OA-related biomarkers. Conclusions: Although many OA-related biomarkers are currently available they exist in various states of qualification and validation. The biomarkers that are likely to have the earliest beneficial impact on clinical trials fall into two general categories, those that will allow targeting of subjects most likely to either respond and/or progress (prognostic value) within a reasonable and manageable time frame for a clinical study (for instance within 1-2 years for an OA trial), and those that provide early feedback for preclinical decision-making and for trial organizers that a drug is having the desired biochemical effect. As in vitro biomarkers are increasingly investigated in the context of specific drug treatments, advances in the field can be expected that will lead to rapid expansion of the list of available biomarkers with increasing understanding of the molecular processes that they represent. (C) 2011 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:515 / 542
页数:28
相关论文
共 127 条
[1]
Recommendations for the use of new methods to assess the efficacy of disease-modifying drugs in the treatment of osteoarthritis [J].
Abadie, E ;
Ethgen, D ;
Avouac, B ;
Bouvenot, G ;
Branco, J ;
Bruyere, O ;
Calvo, G ;
Devogelaer, JP ;
Dreiser, RL ;
Herrero-Beaumont, G ;
Kahan, A ;
Kreutz, G ;
Laslop, A ;
Lemme, EM ;
Nuki, G ;
Van de Putte, L ;
Vanhaelst, L ;
Reginster, JY .
OSTEOARTHRITIS AND CARTILAGE, 2004, 12 (04) :263-268
[2]
Whole-Body Bone Scintigraphy Provides a Measure of the Total-Body Burden of Osteoarthritis for the Purpose of Systemic Biomarker Validation [J].
Addison, Shelby ;
Coleman, R. Edward ;
Feng, Sheng ;
McDaniel, Gary ;
Kraus, Virginia Byers .
ARTHRITIS AND RHEUMATISM, 2009, 60 (11) :3366-3373
[3]
THE AMERICAN-COLLEGE-OF-RHEUMATOLOGY CRITERIA FOR THE CLASSIFICATION AND REPORTING OF OSTEOARTHRITIS OF THE HIP [J].
ALTMAN, R ;
ALARCON, G ;
APPELROUTH, D ;
BLOCH, D ;
BORENSTEIN, D ;
BRANDT, K ;
BROWN, C ;
COOKE, TD ;
DANIEL, W ;
FELDMAN, D ;
GREENWALD, R ;
HOCHBERG, M ;
HOWELL, D ;
IKE, R ;
KAPILA, P ;
KAPLAN, D ;
KOOPMAN, W ;
MARINO, C ;
MCDONALD, E ;
MCSHANE, DJ ;
MEDSGER, T ;
MICHEL, B ;
MURPHY, WA ;
OSIAL, T ;
RAMSEYGOLDMAN, R ;
ROTHSCHILD, B ;
WOLFE, F .
ARTHRITIS AND RHEUMATISM, 1991, 34 (05) :505-514
[4]
THE AMERICAN-COLLEGE-OF-RHEUMATOLOGY CRITERIA FOR THE CLASSIFICATION AND REPORTING OF OSTEOARTHRITIS OF THE HAND [J].
ALTMAN, R ;
ALARCON, G ;
APPELROUTH, D ;
BLOCH, D ;
BORENSTEIN, D ;
BRANDT, K ;
BROWN, C ;
COOKE, TD ;
DANIEL, W ;
GRAY, R ;
GREENWALD, R ;
HOCHBERG, M ;
HOWELL, D ;
IKE, R ;
KAPILA, P ;
KAPLAN, D ;
KOOPMAN, W ;
LONGLEY, S ;
MCSHANE, DJ ;
MEDSGER, T ;
MICHEL, B ;
MURPHY, W ;
OSIAL, T ;
RAMSEYGOLDMAN, R ;
ROTHSCHILD, B ;
STARK, K ;
WOLFE, F .
ARTHRITIS AND RHEUMATISM, 1990, 33 (11) :1601-1610
[5]
DEVELOPMENT OF CRITERIA FOR THE CLASSIFICATION AND REPORTING OF OSTEOARTHRITIS - CLASSIFICATION OF OSTEOARTHRITIS OF THE KNEE [J].
ALTMAN, R ;
ASCH, E ;
BLOCH, D ;
BOLE, G ;
BORENSTEIN, D ;
BRANDT, K ;
CHRISTY, W ;
COOKE, TD ;
GREENWALD, R ;
HOCHBERG, M ;
HOWELL, D ;
KAPLAN, D ;
KOOPMAN, W ;
LONGLEY, S ;
MANKIN, H ;
MCSHANE, DJ ;
MEDSGER, T ;
MEENAN, R ;
MIKKELSEN, W ;
MOSKOWITZ, R ;
MURPHY, W ;
ROTHSCHILD, B ;
SEGAL, M ;
SOKOLOFF, L ;
WOLFE, F .
ARTHRITIS AND RHEUMATISM, 1986, 29 (08) :1039-1049
[6]
Serum levels of Cartilage Oligomeric Matrix Protein (COMP) increase temporarily after physical exercise in patients with knee osteoarthritis [J].
Andersson, Maria L. E. ;
Thorstensson, Carina A. ;
Roos, Ewa M. ;
Petersson, Ingemar F. ;
Heinegard, Dick ;
Saxne, Tore .
BMC MUSCULOSKELETAL DISORDERS, 2006, 7 (1)
[7]
Soy protein may alleviate osteoarthritis symptoms [J].
Arjmandi, BH ;
Khalil, DA ;
Lucas, EA ;
Smith, BJ ;
Sinichi, N ;
Hodges, SB ;
Juma, S ;
Munson, ME ;
Payton, ME ;
Tivis, RD ;
Svanborg, A .
PHYTOMEDICINE, 2004, 11 (7-8) :567-575
[8]
Biomarkers and surrogate endpoints: Preferred definitions and conceptual framework [J].
Atkinson, AJ ;
Colburn, WA ;
DeGruttola, VG ;
DeMets, DL ;
Downing, GJ ;
Hoth, DF ;
Oates, JA ;
Peck, CC ;
Schooley, RT ;
Spilker, BA ;
Woodcock, J ;
Zeger, SL .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2001, 69 (03) :89-95
[9]
ATLEY LM, 1998, T ORTHOP RES SOC, V23, P850
[10]
Differential matrix degradation and turnover in early cartilage lesions of human knee and ankle joints [J].
Aurich, M ;
Squires, GR ;
Reiner, A ;
Mollenhauer, JA ;
Kuettner, KE ;
Poole, AR ;
Cole, AA .
ARTHRITIS AND RHEUMATISM, 2005, 52 (01) :112-119