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临床试验/NCT07056621
NCT07056621招募中不适用

Does Belimumab Modify the Natural History of SLE? A Propensity Score-matched, Real-world Study

Biomedical Research Foundation, Academy of Athens1 个研究点 分布在 1 个国家目标入组 684 人开始时间: 2025年6月30日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
684
试验地点
1
主要终点
Bilag A flare

研究概览

简要总结

This will be a combined retrospective and prospective cohort study, that will evaluate the incidence of de novo Systemic Lupus Erythematosus major organ manifestations (defined as BILAG A flares) in patients receiving belimumab (Arm A) and compare it to 2 standard-of-care groups (SoC) (Arm B: patients on SoC; Arm C: patients on SoC followed-up up to May 1st 2014, the first date where belimumab was available in Greece).

The investigators will utilize survival analysis methods (Kaplan-Meier survival curves and Cox regression) and mixed effects longitudinal analyses. Additionally, the investigators will employ propensity score matching and/or inverse probability of treatment weighting, to create balanced cohorts and reduce bias.

详细描述

Belimumab (BEL) has been used for the treatment of SLE for over 10 years, with clear evidence for a beneficial effect in reduction of disease activity and frequency of flares, as well as prevention of damage accrual.

Whether BEL may also result in prevention of incident, major organ involvement in patients with SLE is less clear. A recent post-hoc analysis of the BLISS trials suggested that BEL (although at the low, rather than standard-dose) reduced the rate of de novo renal flares (defined by BILAG) compared to standard-of-care but real-life data are scarce. Importantly, data on the ability of belimumab to decrease major neuropsychiatric events in SLE such as strokes, seizures and cognitive dysfunction or other severe manifestations such as severe hematologic or cardiopulmonary disease is not known.

To this end, the investigators propose a propensity score-matched, real-world, with the use of longitudinal data from large patient cohorts and time-to-event analyses. Given the non-experimental setting of this study, the investigators will also employ propensity score matching (PSM), to create balanced cohorts of BEL-treated and non-BEL-treated patients and reduce bias in estimating treatment efficacy.

The study will consist of 3 arms, as follows: Arm A: patients on treatment with belimumab; Arm B: patients on standard-of-care (SoC) treatment from May 1st 2014 onwards; Arm C: a historical cohort of patients on SoC followed-up up to May 1st 2014, the first date where belimumab was available in Greece.

研究设计

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

入排标准

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

入选标准

  • •Systemic lupus erythematosus classification according to the Systemic Lupus International Collaborating Clinics (SLICC) criteria
  • •Age ≥ 18 years old
  • •Time of follow-up ≥ 6 months
  • •Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) ≥ 4
  • •Physician Global Assessment (PGA) visual analogue score > 1

排除标准

  • •Patients with incomplete medical records or missing key variables
  • •Patients with concomitant autoimmune disorders (excluding thyroid disease)

结局指标

主要结局

Bilag A flare

时间窗: From enrollment to the end of treatment (expected follow-up duration 1-4 years).

Major organ systemic lupus erythematosus manifestations as defined by the BILAG (British Isles Lupus Assessment Group) index (BILAG A flare)

次要结局

  • SLICC/ACR Damage Index(From enrollment to the end of treatment (expected follow-up duration 1-4 years).)

研究者

发起方
Biomedical Research Foundation, Academy of Athens
申办方类型
Other
责任方
Principal Investigator
主要研究者

DIMITRIOS BOUMPAS

Professor in Medicine

Biomedical Research Foundation, Academy of Athens

研究点 (1)

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