How to define responders in osteoarthritis

被引:84
作者
Cooper, Cyrus [1 ]
Adachi, Jonathan D. [2 ]
Bardin, Thomas [3 ,4 ]
Berenbaum, Francis [5 ,6 ]
Flamion, Bruno [7 ]
Jonsson, Helgi [8 ]
Kanis, John A. [9 ]
Pelousse, Franz [10 ]
Lems, Willem F. [11 ]
Pelletier, Jean-Pierre [12 ]
Martel-Pelletier, Johanne [12 ]
Reiter, Susanne [13 ]
Reginster, Jean-Yves [14 ,15 ]
Rizzoli, Rene [16 ,17 ]
Bruyere, Olivier [14 ,15 ]
机构
[1] Univ Southampton, MRC Epidemiol Resource Ctr, Southampton, Hants, England
[2] McMaster Univ, Dept Med, Div Rheumatol, Hamilton, ON, Canada
[3] Lariboisiere Hosp, AP HP, Dept Rheumatol, Paris, France
[4] Univ Paris 07, Paris, France
[5] Hop St Antoine, AP HP, Dept Rheumatol, F-75571 Paris, France
[6] Univ Paris 06, Paris, France
[7] Univ Namur, Lab Physiol & Pharmacol, URPhyM, NARILIS, Namur, Belgium
[8] Univ Iceland, Landspitalinn Univ Hosp, Reykjavik, Iceland
[9] Univ Sheffield, Sch Med, WHO Collaborating Ctr Metab Bone Dis, Sheffield, S Yorkshire, England
[10] CHR Citadelle, Dept Radiodiag, Liege, Belgium
[11] Vrije Univ Amsterdam Med Ctr, Dept Rheumatol, Amsterdam, Netherlands
[12] Univ Montreal, Notre Dame Hosp, Univ Montreal Hosp Res Ctr CRCHUM, Osteoarthritis Res Unit, Montreal, PQ H3C 3J7, Canada
[13] Fed Inst Drugs & Med Devices BfArM, Bonn, Germany
[14] Univ Liege, Dept Publ Hlth Sci, B-4000 Liege, Belgium
[15] CHU Ctr Ville, Liege, Belgium
[16] Univ Hosp Geneva, Dept Rehabil & Geriatr, Div Bone Dis, Geneva, Switzerland
[17] Fac Med Geneva, Geneva, Switzerland
关键词
Magnetic resonance imaging; Osteoarthritis; Pain; Responder; Structure-modifying drug; X-ray; TOTAL JOINT REPLACEMENT; PATIENT REPORTED OUTCOMES; TOTAL KNEE ARTHROPLASTY; TOTAL HIP-ARTHROPLASTY; DOUBLE-BLIND; GLUCOSAMINE SULFATE; BIOCHEMICAL MARKERS; CARTILAGE LOSS; CHONDROITINS; RISK-FACTORS;
D O I
10.1185/03007995.2013.792793
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background: Osteoarthritis is a clinical syndrome of failure of the joint accompanied by varying degrees of joint pain, functional limitation, and reduced quality of life due to deterioration of articular cartilage and involvement of other joint structures. Scope: Regulatory agencies require relevant clinical benefit on symptoms and structure modification for registration of a new therapy as a disease-modifying osteoarthritis drug (DMOAD). An international Working Group of the European Society on Clinical and Economic Aspects of Osteoporosis and Osteoarthritis (ESCEO) and International Osteoporosis Foundation was convened to explore the current burden of osteoarthritis, review current regulatory guidelines for the conduct of clinical trials, and examine the concept of responder analyses for improving drug evaluation in osteoarthritis. Findings: The ESCEO considers that the major challenges in DMOAD development are the absence of a precise definition of the disease, particularly in the early stages, and the lack of consensus on how to detect structural changes and link them to clinically meaningful endpoints. Responder criteria should help identify progression of disease and be clinically meaningful. The ideal criterion should be sensitive to change over time and should predict disease progression and outcomes such as joint replacement. Conclusion: The ESCEO considers that, for knee osteoarthritis, clinical trial data indicate that radiographic joint space narrowing >0.5mm over 2 or 3 years might be a reliable surrogate measure for total joint replacement. On-going research using techniques such as magnetic resonance imaging and biochemical markers may allow the identification of these patients earlier in the disease process.
引用
收藏
页码:719 / 729
页数:11
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