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临床试验/NCT02927535
NCT02927535已完成不适用

Evaluation of TNFα Blockers Monotherapy in Early Rheumatoid Arthritis in France

Centre Hospitalier Universitaire de Nīmes1 个研究点 分布在 1 个国家目标入组 813 人开始时间: 2016年1月15日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
813
试验地点
1
主要终点
Frequency of use of TNF blocker monotherapy

研究概览

简要总结

Aim: To describe 1) The use of TNF blockers monotherapy in early arthritis in daily clinical practice in France 2) To evaluate symptomatic, structural efficacy, and retention rate over 5 years of TNF blockers monotherapy 3) To evaluate predictive factors for TNF blocker response monotherapy Type of study: Observational cohort study using cross-section and longitudinal data.

Description of the project methodology

  • Patients: All patients in the ESPOIR cohort (multicentre French cohort study of early RA).A sub-analysis will be conducted among patients satisfying the ACR-EULAR 2010 criteria.
  • Data collected: Patient characteristics, Clinical data regarding RA and related pathologies, Characteristics of treatments received The analysis will be conducted using data collected at baseline, 6, 12, 18, 24, 36, 48, 60 months.
  • Analyses:
  1. Frequency of use of TNF blockers monotherapy: we will calculate the % of patients initiating TNF blockers monotherapy (Kaplan-Meier method), and we will describe the type of TNF blocker, the route of administration, the dosage, and the place of the TNF blockers monotherapy in the treatment strategy during the first 5 years.
  2. Identification of potential predictive factors for initiation of TNF blockers monotherapy: a survival curve (Kaplan-Meier) will be performed. The baseline characteristics of the patients with regard to the initiation of TNF blocker monotherapy during the first 5 years of the disease will be compared by univariate analysis and Log-rank test will be performed in all variables. A stepwise multivariate analysis (Cox analysis) will be performed.
  3. Therapeutical effect: we will calculate the retention rate over time, and will compare the changes in different variables in the group of patients who have received TNF blockers monotherapy matched (using a propensity score) to 1,2 or 3 patients who have received TNF blockers in combination with synthetic DMARDs. We will assess and compare DAS28 and HAQ at short term (after at least 8 weeks of treatment) and long term (last available visit) in groups. The structural efficacy was evaluated by the radiographic progression at last available visit. We will identically estimate the drug effect depending on the TNF blocker used, by calculating the retention rate and comparing DAS28 at short term and long term.
  4. Identification of predictive factors for TNF blocker monotherapy response: To evaluate the impact of baseline demographics and disease conditions on the DAS28 and HAQ response during the first 5 years will be compared by univariate and multivariate analysis.

Expected results:

Increase knowledge on the use of TNF blocker monotherapy, its efficacy and retention rate, and on predictive factors for TNF blocker monotherapy response in early RA patients.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age 18 to 70 years
  • more than 2 swollen joints for >6 weeks and <6 months
  • suspected or confirmed diagnosis of RA
  • no previous intake of DMARDs or steroids (except if <2 weeks).

排除标准

  • Patients were excluded if the referring physician judged they had other clearly defined inflammatory rheumatic diseases.

结局指标

主要结局

Frequency of use of TNF blocker monotherapy

时间窗: 120 months

Frequency of use of TNF blocker monotherapy

时间窗: baseline (day 0)

Frequency of use of TNF blocker monotherapy

时间窗: 6 months

Frequency of use of TNF blocker monotherapy

时间窗: 12 months

Frequency of use of TNF blocker monotherapy

时间窗: 18 months

Frequency of use of TNF blocker monotherapy

时间窗: 24 months

Frequency of use of TNF blocker monotherapy

时间窗: 36 months

Frequency of use of TNF blocker monotherapy

时间窗: 48 months

Frequency of use of TNF blocker monotherapy

时间窗: 60 months

次要结局

未报告次要终点

研究者

发起方
Centre Hospitalier Universitaire de Nīmes
申办方类型
Other
责任方
Sponsor

研究点 (1)

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