Tanezumab for the Treatment of Pain from Osteoarthritis of the Knee

被引:498
|
作者
Lane, Nancy E. [1 ]
Schnitzer, Thomas J. [2 ]
Birbara, Charles A. [3 ]
Mokhtarani, Masoud [4 ]
Shelton, David L. [4 ]
Smith, Mike D. [5 ]
Brown, Mark T. [5 ]
机构
[1] Univ Calif Davis, Sch Med, Dept Med, Sacramento, CA 95817 USA
[2] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
[3] Univ Massachusetts, Sch Med, Worcester, MA USA
[4] Rinat Neurosci, San Francisco, CA USA
[5] Pfizer, New London, CT USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2010年 / 363卷 / 16期
基金
美国国家卫生研究院;
关键词
NERVE GROWTH-FACTOR; CLINICAL-TRIALS; NGF; METAANALYSIS; ARTHRITIS; AFFINITY; CRITERIA; RECEPTOR; SULFATE; DRUGS;
D O I
10.1056/NEJMoa0901510
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Increased expression of nerve growth factor in injured or inflamed tissue is associated with increased pain. This proof-of-concept study was designed to investigate the safety and analgesic efficacy of tanezumab, a humanized monoclonal antibody that binds and inhibits nerve growth factor. METHODS We randomly assigned 450 patients with osteoarthritis of the knee to receive tanezumab (administered at a dose of 10, 25, 50, 100, or 200 mu g per kilogram of body weight) or placebo on days 1 and 56. The primary efficacy measures were knee pain while walking and the patient's global assessment of response to therapy. We also assessed pain, stiffness, and physical function using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC); the rate of response using the criteria of the Outcome Measures for Rheumatology Committee and Osteoarthritis Research Society International Standing Committee for Clinical Trials Response Criteria Initiative (OMERACT-OARSI); and safety. RESULTS When averaged over weeks 1 through 16, the mean reductions from baseline in knee pain while walking ranged from 45 to 62% with various doses of tanezumab, as compared with 22% with placebo (P<0.001). Tanezumab, as compared with placebo, was also associated with significantly greater improvements in the response to therapy as assessed with the use of the patients' global assessment measure (mean increases in score of 29 to 47% with various doses of tanezumab, as compared with 19% with placebo; P <= 0.001). The rate of response according to the OMERACT-OARSI criteria ranged from 74 to 93% with tanezumab treatment, as compared with 44% with placebo (P<0.001). The rates of adverse events were 68% and 55% in the tanezumab and placebo groups, respectively. The most common adverse events among tanezumab-treated patients were headache (9% of the patients), upper respiratory tract infection (7%), and paresthesia (7%). CONCLUSIONS In this proof-of-concept study, treatment with tanezumab was associated with a reduction in joint pain and improvement in function, with mild and moderate adverse events, among patients with moderate-to-severe osteoarthritis of the knee.
引用
收藏
页码:1521 / 1531
页数:11
相关论文
共 50 条
  • [31] Pooled analysis of tanezumab efficacy and safety with subgroup analyses of phase III clinical trials in patients with osteoarthritis pain of the knee or hip
    Tive, Leslie
    Bello, Alfonso E.
    Raclin, David
    Schnitzer, Thomas J.
    Nguyen, Ha
    Brown, Mark T.
    West, Christine R.
    JOURNAL OF PAIN RESEARCH, 2019, 12 : 975 - 995
  • [32] Subcutaneous tanezumab for osteoarthritis: Is the early improvement in pain and function meaningful and sustained?
    Berenbaum, Francis
    Langford, Richard
    Perrot, Serge
    Miki, Kenji
    Blanco, Francisco J.
    Yamabe, Takaharu
    Isogawa, Naoki
    Junor, Rod
    Carey, William
    Viktrup, Lars
    West, Christine R.
    Brown, Mark T.
    Verburg, Kenneth M.
    EUROPEAN JOURNAL OF PAIN, 2021, 25 (07) : 1525 - 1539
  • [33] Association of Knee Pain Patterns Determined From the Intermittent and Constant Osteoarthritis Pain Instrument with Knee Pain Severity: The Multicenter Osteoarthritis Study
    Neogi, Tuhina
    Niu, Jingbo
    Felson, David T.
    Nevitt, Michael C.
    Lewis, C. E.
    Torner, James
    French, Melissa
    Hawker, Gillian A.
    ARTHRITIS AND RHEUMATISM, 2011, 63 (10): : S636 - S637
  • [34] Responsiveness of the Intermittent and Constant Osteoarthritis Pain (ICOAP) scale in a trial of duloxetine for treatment of osteoarthritis knee pain
    Risser, R. C.
    Hochberg, M. C.
    Gaynor, P. J.
    D'Souza, D. N.
    Frakes, E. P.
    OSTEOARTHRITIS AND CARTILAGE, 2013, 21 (05) : 691 - 694
  • [35] Surgical Knee Denervation for the Treatment of Pain Caused by Primary Osteoarthritis
    Hustedt, Joshua W.
    Reichenbach, Rachel
    Merrell, Dallin
    Watzig, Ben
    Robainia, Joey
    Silvestri, Brianna
    PLASTIC AND RECONSTRUCTIVE SURGERY, 2024, 154 (01) : 228 - 234
  • [36] SYNTHETIC TRANSDERMAL CANNABIDIOL FOR THE TREATMENT OF KNEE PAIN DUE TO OSTEOARTHRITIS
    Hunter, D.
    Oldfield, G.
    Tich, N.
    Messenheimer, J.
    Sebree, T.
    OSTEOARTHRITIS AND CARTILAGE, 2018, 26 : S26 - S26
  • [37] Conditioned pain modulation and treatment response in patients with knee osteoarthritis
    Cornelius, M.
    Edwards, R.
    JOURNAL OF PAIN, 2014, 15 (04): : S96 - S96
  • [38] INTERACTIONS OF JOINT KINEMATICS AND PHARMACOLOGIC TREATMENT FOR KNEE OSTEOARTHRITIS PAIN
    Boyer, K. A.
    Andiracchi, K.
    Andriacchi, T. P.
    OSTEOARTHRITIS AND CARTILAGE, 2013, 21 : S98 - S99
  • [39] Genicular Artery Embolization for the Treatment of Knee Pain Secondary to Osteoarthritis
    Bagla, Sandeep
    Piechowiak, Rachel
    Hartman, Terry
    Orlando, Julie
    Del Gaizo, Daniel
    Isaacson, Ari
    JOURNAL OF VASCULAR AND INTERVENTIONAL RADIOLOGY, 2020, 31 (07) : 1096 - 1102
  • [40] EFFICIENCY OF INTRA-ARTICULAR TREATMENT ON PAIN IN KNEE OSTEOARTHRITIS
    Rogoveanu, O. C.
    Cioroianu, G. O.
    Gofita, C.
    Musetescu, A.
    Traistaru, R.
    OSTEOPOROSIS INTERNATIONAL, 2021, 32 (SUPPL 1) : S168 - S168