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学科主题: 临床医学
题名:
Tofacitinib in Combination With Nonbiologic Disease-Modifying Antirheumatic Drugs in Patients With Active Rheumatoid Arthritis A Randomized Trial
作者: Kremer, Joel; Li, Zhan-Guo; Hall, Stephen; Fleischmann, Roy; Genovese, Mark; Martin-Mola, Emilio; Isaacs, John D.; Gruben, David; Wallenstein, Gene; Krishnaswami, Sriram; Zwillich, Samuel H.; Koncz, Tamas; Riese, Richard9; Bradley, John
刊名: ANNALS OF INTERNAL MEDICINE
发表日期: 2013-08-20
卷: 159, 期:4, 页:253-+
收录类别: SCI
文章类型: Article
WOS标题词: Science & Technology
类目[WOS]: Medicine, General & Internal
研究领域[WOS]: General & Internal Medicine
关键词[WOS]: INADEQUATE RESPONSE ; JAK INHIBITOR ; METHOTREXATE ; CP-690,550 ; PLACEBO ; ADALIMUMAB ; MALIGNANCY ; EFFICACY ; SAFETY ; RISK
英文摘要:

Background: Many patients with rheumatoid arthritis (RA) do not achieve adequate and safe responses with disease-modifying antirheumatic drugs (DMARDs). Tofacitinib is a novel, oral, Janus kinase inhibitor that treats RA.

Objective: To evaluate the efficacy and safety of tofacitinib in combination with nonbiologic DMARDs.

Design: 1-year, double-blind, randomized trial (ClinicalTrials.gov:NCT00856544).

Setting: 114 centers in 19 countries.

Patients: 792 patients with active RA despite nonbiologic DMARD therapy.

Intervention: Patients were randomly assigned 4:4:1:1 to oral tofacitinib, 5 mg or 10 mg twice daily, or placebo advanced to tofacitinib, 5 mg or 10 mg twice daily.

Measurements: Primary end points were 20% improvement in American College of Rheumatology (ACR20) criteria; Disease Activity Score for 28-joint counts based on the erythrocyte sedimentation rate (DAS28-4[ESR]) of less than 2.6; DAS28-4(ESR)-defined remission, change in Health Assessment Questionnaire Disability Index (HAQ-DI) score, and safety assessments.

Results: Mean treatment differences for ACR20 response rates (month 6) for the 5-mg and 10-mg tofacitinib groups compared with the combined placebo groups were 21.2% (95% CI, 12.2% to 30.3%; P < 0.001) and 25.8% (CI, 16.8% to 34.8%; P < 0.001), respectively. The HAQ-DI scores (month 3) and DAS28-4( ESR) less than 2.6 response rates (month 6) were also superior in the tofacitinib groups versus placebo. The incidence rates of serious adverse events for patients receiving 5-mg tofacitinib, 10-mg tofacitinib, or placebo were 6.9, 7.3, or 10.9 events per 100 patient-years of exposure, respectively. In the tofacitinib groups, 2 cases of tuberculosis, 2 cases of other opportunistic infections, 3 cardiovascular events, and 4 deaths occurred. Neutrophil counts decreased, hemoglobin and low-and high-density lipoprotein cholesterol levels increased, and serum creatinine levels had small increases in the tofacitinib groups

Limitations: Placebo groups were smaller and of shorter duration. Patients received primarily methotrexate. The ability to assess drug combinations other than tofacitinib plus methotrexate was limited.

Conclusion: Tofacitinib improved disease control in patients with active RA despite treatment with nonbiologic DMARDs, primarily methotrexate.

语种: 英语
项目资助者: Pfizer
WOS记录号: WOS:000323421700015
Citation statistics:
内容类型: 期刊论文
URI标识: http://ir.bjmu.edu.cn/handle/400002259/65841
Appears in Collections:北京大学第二临床医学院_期刊论文

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作者单位: 1.Albany Med Coll, Albany, NY 12208 USA
2.Peking Univ, Peoples Hosp, Beijing 100871, Peoples R China
3.Cabrini Med Ctr, Malvern, Vic, Australia
4.Metroplex Clin Res Ctr, Dallas, TX USA
5.Stanford Univ, Stanford, CA 94305 USA
6.Hosp Univ La Paz, Madrid, Spain
7.Newcastle Univ, Newcastle Biomed Res Ctr, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
8.Newcastle Tyne Hosp NHS Trust, Newcastle Upon Tyne, Tyne & Wear, England
9.Pfizer Inc, Groton, CT 06340 USA
10.Pfizer, New York, NY USA

Recommended Citation:
Kremer, Joel,Li, Zhan-Guo,Hall, Stephen,et al. Tofacitinib in Combination With Nonbiologic Disease-Modifying Antirheumatic Drugs in Patients With Active Rheumatoid Arthritis A Randomized Trial[J]. ANNALS OF INTERNAL MEDICINE,2013,159(4):253-+.
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