A Phase IV, Randomized, Multi-center Clinical Trial to Compare the Efficacy of Orbital Radiotherapy in Association With Intravenous Glucocorticoids vs Intravenous Glucocorticoids Alone for Moderately Severe and Active Graves' Orbitopathy
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 入组人数
- 120
- 主要终点
- Comparison of overall GO outcome determined using a composite evaluation
研究概览
简要总结
Graves' orbitopathy (GO) is a disfiguring and disabling disease that profoundly impairs the quality of life of affected patients. High dose intravenous (iv) glucocorticoids (GC) (ivGC) is a well established, widely used treatment for active GO. The use of systemic glucocorticoids takes advantage from their immune suppressive and antiinflammatory actions, resulting in an overall beneficial effect ranging from ~35 to ~60% of patients in various studies. The intravenous route of administration has been shown to be superior to the oral route, both in terms of GO outcome and side effect profile. The combination of ivGC and orbital radiotherapy (OR) is used routinely in patients with moderate-severe, active GO, as a second-line treatment, as also recommended in the recent Guidelines published by the European Thyroid Association/European Group on Graves' Orbitopathy. Thus, the majority of studies have shown that OR increases the response rate to GC. Those studies were performed using oral GC, whereas it is not known whether OR potentiate also the effects of ivGC.
The present study is aimed at determining whether OR potentiate the effects of ivGC in the treatment of moderately severe and active GO, in terms of GO outcome and quality of life. A possible extension of the study can be foreseen, aimed at investigating the very long time GO outcome.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Investigator)
盲法说明
Ophthalmology blinded to treatment
入排标准
- 年龄范围
- 35 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •A diagnosis of Graves' disease based on the presence of hyperthyroidism (either untreated or treated with antithyroid drugs) associated with detectable anti-TSH receptor autoantibodies
- •No major treatments for hyperthyroidism (thyroidectomy or radioiodine) in the last 3 months
- •Euthyroidism on anti-thyroid medications or L'thyroxine (LT4) since at least 2 months
- •GO symptoms lasting since no more than one year
- •Active GO: CAS ≥ 3 out of 7 (worst eye)
- •Moderate or moderately severe GO: at least one of the following signs (worst eye):
- •Exophthalmos ≥ 22 mm
- •Eye muscle involvement with mono-ocular ductions in any direction of gaze of less than 30° or evident dismotility
- •Diplopia according to Gorman score of grades a-c
- •No corticosteroids or immunosuppressive treatment for GO in the last 3 months
- •No contraindication to OR: diabetes, hypertension, retinopathy of any type, glaucoma
- •Male and female patients of age: 35-75 years
- •Effective method of contraception during the whole trial and at least six weeks after last intake of trial drugs (only female of reproducing age)
- •No mental illness that prevent patients from comprehensive, written informed consent
- •Compliant patient, regular follow-up possible
排除标准
- •Absence of Graves' hyperthyroidism (present or past)
- •Thyroidectomy or radioiodine in the last 3 months
- •Uncontrolled hyperthyroidism or hypothyroidism
- •GO symptoms lasting since more than one year
- •CAS <3 (worst eye)
- •Optic neuropathy
- •Contraindications to OR (diabetes, retinopathy of any kind)
- •Pregnancy, breast-feeding women
- •No informed consent
- •Acute or chronic liver disease
- •Relevant Malignancy
- •Chronic renal failure or other diseases of any relevance to prevent steroid treatment 13) Corticosteroids or other immunosuppressive agents within last 3 months
- •Recent (≤1 year) history of alcoholism or drug abuse
- •Previous orbital disease other than GO, eye injuries or surgery
研究组 & 干预措施
No Radiotherapy
Patients with moderately severe GO treated with Intravenous glucocorticoids alone
干预措施: Methylprednisolone (Drug)
Radiotherapy
Patients with moderately severe GO treated with Intravenous glucocorticoids associated with orbital radiotherapy
干预措施: Orbital radiotherapy (Radiation)
Radiotherapy
Patients with moderately severe GO treated with Intravenous glucocorticoids associated with orbital radiotherapy
干预措施: Methylprednisolone (Drug)
结局指标
主要结局
Comparison of overall GO outcome determined using a composite evaluation
时间窗: 52 weeks
A composite evaluation of GO was described previously. Improvement is defined as amelioration of two parameters in at least one eye, without deterioration of any parameters in both eyes: Deterioration is defined as worsening in two parameters in at least one eye: All other cases are defined as "no change" The parameters are: * Eyelid swelling (improvement/worsening according to EUGOGO Atlas evaluation) * Lid aperture in mm (significant variation: 2 or more mm) * Clinical activity score (CAS) (7 items: spontaneous pain, evoked pain, eyelid edema, eyelid redness, conjunctiva redness, caruncle edema, chemosis; significant change: at least 2 points) * Exophthalmos in mm (significant variation 2 or more mm) * Eye muscle involvement - diplopia score (Gorman score) (significant variation: disappearance or change in the degree, or improvement of ≥12 degrees in motility)
次要结局
- Comparison of overall GO outcome determined using a composite evaluation(26 weeks)
- Comparison of a disease specific quality of life questionnaire (GO-QoL)(52 weeks)
- GO relapse(52 weeks)
研究者
Marinò Michele
Ricercatore (Assistant Professor)
University of Pisa