Infliximab (chimeric anti-tumour necrosis factor α monoclonal antibody) versus placebo in rheumatoid arthritis patients receiving concomitant methotrexate:: a randomised phase III trial

被引:1972
作者
Maini, R [1 ]
St Clair, EW
Breedveld, F
Furst, D
Kalden, J
Weisman, M
Smolen, J
Emery, P
Harriman, G
Feldmann, M
Lipsky, P
机构
[1] Kennedy Inst Rheumatol, London W8 8LH, England
[2] Charing Cross Hosp, Imperial Coll, Sch Med, London W8 8LH, England
[3] Duke Univ, Durham, NC USA
[4] Leiden Univ, Leiden, Netherlands
[5] Virginia Mason Res Ctr, Seattle, WA 98101 USA
[6] Inst Clin Immunol & Rheumatol, Erlangen, Germany
[7] Univ Calif San Diego, La Jolla, CA 92093 USA
[8] Univ Vienna, A-1010 Vienna, Austria
[9] Univ Leeds, Rheumatol & Rehabil Res Unit, Leeds LS2 9JT, W Yorkshire, England
[10] Centocor Inc, Malvern, PA 19355 USA
[11] Univ Texas, SW Med Ctr, Dallas, TX USA
关键词
D O I
10.1016/S0140-6736(99)05246-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Not all patients with rheumatoid arthritis can tolerate or respond to methotrexate, a standard treatment for this disease. There is evidence that antitumour necrosis factor alpha (TNF alpha) is efficacious in relief of signs and symptoms. We therefore investigated whether infliximab, a chimeric human-mouse anti-TNF alpha monoclonal antibody would provide additional clinical benefit to patients who had active rheumatoid arthritis despite receiving methotrexate. Methods In an international double-blind placebo-controlled phase III clinical trial, 428 patients who had active rheumatoid arthritis, who had received continuous methotrexate for at least 3 months and at a stable dose for at least 4 weeks, were randomised to placebo (n=88) or one of four regimens of infliximab at weeks 0, 2, and 6. Additional infusions of the same dose were given every 4 or 8 weeks thereafter on a background of a stable dose of methotrexate (median 15 mg/week for greater than or equal to 6 months; range 10-35 mg/wk). Patients were assessed every 4 weeks for 30 weeks. Findings At 30 weeks, the American College of Rheumatology (20) response criteria, representing a 20% improvement from baseline, were achieved in 53, 50, 58, and 52% of patients receiving 3 mg/kg every 4 or 8 weeks or 10 mg/kg every 4 or 8 weeks, respectively, compared with 20% of patients receiving placebo plus methotrexate (p<0.001 for each of the four infliximab regimens vs placebo). A 50% improvement was achieved in 29, 27, 26, and 31% of infliximab plus methotrexate in the same treatment groups, compared with 5% of patients on placebo plus methotrexate (p<0.001). Infliximab was well-tolerated; withdrawals for adverse events as well as the occurrence of serious adverse events or serious infections did not exceed those in the placebo group. Interpretation During 30 weeks, treatment with infliximab plus methotrexate was more efficacious than methotrexate alone in patients with active rheumatoid arthritis not previously responding to methotrexate.
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收藏
页码:1932 / 1939
页数:8
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