The treatment of disc herniation-induced sciatica with infliximab -: Results of a randomized, controlled, 3-month follow-up study

被引:87
作者
Korhonen, T
Karppinen, J
Paimela, L
Malmivaara, A
Lindgren, KA
Järvinen, S
Niinimäki, J
Veeger, N
Seitsalo, S
Hurri, H
机构
[1] Oulu Univ Hosp, Dept Phys Med & Rehabil, Oulu 90029, Finland
[2] Oulu Univ Hosp, Dept Diagnost Radiol, Oulu, Finland
[3] Finnish Inst Occupat Hlth, Dept Occupat Med, Helsinki, Finland
[4] ORTON Orthopaed Hosp, Helsinki, Finland
[5] Finnish Off Hlth Care Technol Assessment, Helsinki, Finland
[6] Univ Groningen Hosp, Trial Coordinat Ctr, Groningen, Netherlands
关键词
lumbar radicular pain; sciatica; disc herniation; cytokine; TNF; infliximab; randomized controlled trial;
D O I
10.1097/01.brs.0000190815.13764.64
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Design. A randomized controlled trial. Objectives. To evaluate the efficacy of infliximab, a monoclonal antibody against tumor necrosis factor (TNF)-alpha in a randomized controlled setting. Summary of Background Data. Recently, we obtained encouraging results in an open-label study of infliximab in patients with disc herniation-induced sciatica. Furthermore, the results of experimental studies support the use of infliximab in sciatica. Therefore, we initiated a randomized, controlled trial (FIRST II, Finnish Infliximab Related STudy) to confirm the efficacy of a single infusion of infliximab for sciatic pain. Methods. Inclusion criteria were unilateral moderate to severe sciatic pain with an MRI-confirmed disc herniation concordant with the symptoms and signs of radicular pain. Patients had to be candidates for discectomy, as evaluated by an independent orthopedic surgeon. Forty patients were allocated to a single intravenous infusion of either infliximab 5 mg/kg or placebo. Assessments at baseline and various time points included clinical examination with measurement of straight leg raising restriction; questionnaires related to subjective symptoms ( leg and back pain by 100-mm visual analog scale, Oswestry disability); sick leaves; number of discectomies; and adverse effects possibly related to treatment. The primary endpoint was a reduction in leg pain from baseline to 12 weeks, which was analyzed using a Mann-Whitney U test and repeated-measures analysis. Results. A significant reduction in leg pain was observed in both groups, with no significant difference between treatment regimens. Similar efficacy was observed between treatment groups for secondary endpoints. Seven patients in each group required surgery. No adverse effects related to treatment were encountered. Conclusions. The results of this randomized trial do not support the use of infliximab for lumbar radicular pain in patients with disc herniation-induced sciatica.
引用
收藏
页码:2724 / 2728
页数:5
相关论文
共 15 条
[1]  
*AG HLTH CAR POL R, 1994, AC LOW BACK PROBL AD
[2]   Local application of disc-related cytokines on spinal nerve roots [J].
Aoki, Y ;
Rydevik, B ;
Kikuchi, S ;
Olmarker, K .
SPINE, 2002, 27 (15) :1614-1617
[3]   TNF-α blockade for herniated intervertebral disc-induced sciatica:: a way forward at last? [J].
Cooper, RG ;
Freemont, AJ .
RHEUMATOLOGY, 2004, 43 (02) :119-121
[4]   Efficacy of etanercept in the treatment of acute, severe sciatica: a pilot study [J].
Genevay, S ;
Stingelin, S ;
Gabay, C .
ANNALS OF THE RHEUMATIC DISEASES, 2004, 63 (09) :1120-1123
[5]   2000 Volvo Award Winner in Basic Science Studies - Exogenous tumor necrosis factor-alpha mimics nucleus pulposus-induced neuropathology - Molecular, histologic, and behavioral comparisons in rats [J].
Igarashi, T ;
Kikuchi, S ;
Shubayev, V ;
Myers, RR .
SPINE, 2000, 25 (23) :2975-2980
[6]   Tumor necrosis factor-α monoclonal antibody, infliximab, used to manage severe sciatica [J].
Karppinen, J ;
Korhonen, T ;
Malmivaara, A ;
Paimela, L ;
Kyllönen, E ;
Lindgren, KA ;
Rantanen, P ;
Tervonen, O ;
Niinimäki, J ;
Seitsalo, S ;
Hurri, H .
SPINE, 2003, 28 (08) :750-753
[7]  
MARSHALL LL, 1973, LANCET, V2, P320
[8]   THE INFLAMMATORY EFFECT OF NUCLEUS PULPOSUS - A POSSIBLE ELEMENT IN THE PATHOGENESIS OF LOW-BACK-PAIN [J].
MCCARRON, RF ;
WIMPEE, MW ;
HUDKINS, PG ;
LAROS, GS .
SPINE, 1987, 12 (08) :760-764
[9]  
Mixter WJ., 1934, N Engl J Med, V211, P210
[10]  
OLMARKER K, 1993, SPINE, V18, P1425