Impact of Omalizumab Withdrawal After a 3 Year Duration Treatment in Well Controlled Severe Allergic Asthma : a Multicentric Randomized Controlled Trial
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 入组人数
- 234
- 试验地点
- 1
- 主要终点
- Number of exacerbations
研究概览
简要总结
The optimal duration of the treatment by OMA remains unclear when asthma is well controlled. Data suggest that a large part of patients with well controlled asthma can discontinue OMA therapy without any asthma control deterioration or with an acceptable decrease in asthma control, therefore French experts propose that omalizumab can be given for "3 to 5 yrs if asthma remains well controlled".
The costs related to OMA are high and frequent injections represent severe constraints for patients. For all these reasons, evaluating whether shortening duration of OMA therapy is feasible while maintaining acceptable asthma control is a critical point. Therefore, the aim of this study is to evaluate asthma control after OMA discontinuation after at least 33 months of treatment when asthma is well controlled.
详细描述
Omalizumab (OMA) is a monoclonal anti IgE antibody, developed for severe uncontrolled allergic asthma. Efficacy of OMA in this indication is well documented in randomized trials as well as in real life studies, reducing the number of severe exacerbations by about 50% and improving asthma control score .
However, despite commercialized since 2006 in France, the optimal duration of the treatment remains unclear when asthma is well controlled. In particular, there is no guideline to apply the "step down theory" to biologics in well controlled patients.
It seems clear that a treatment given for less than one year is associated with an early relapse of the disease. However, in a randomized controlled study including 176 patients, stopping the treatment after 5 years induced a small, but acceptable loss of control (average decrease of asthma control test (ACT) by 2.88 and 1.16 point, p= 0.18), but some patients had uncontrolled asthma when the treatment was stopped. In a smaller cohort of 49 patients in Spain who voluntarily accepted to discontinue OMA treatment after 6 years of therapy, asthma deterioration (defined by one or more exacerbation and any Asthma Control Test change during the 1st year) was observed in 24% of patients during the first year following discontinuation , with a maximal rate of 2 exacerbations/yr. After 4 years of discontinuation, 60% of patients still take advantage of the 6 yrs of treatment with OMA. A retrospective study in France found that 14/26 patients treated for at least 3 years kept the same level of control after discontinuation. All these data suggest that a large part of patients with well controlled asthma can discontinue OMA therapy without any asthma control deterioration or with an acceptable decrease in asthma control.
Inducing long term asthma remissions, rather than complete cure, is one potential goal of biologics. OMA is supposed to have disease modifying effects , explaining why there is a hope for a good asthma control being maintained after discontinuation. For this reason, French experts propose that omalizumab can be given for "3 to 5 yrs if asthma remains well controlled" . After an asthma relapse, OMA can be prescribed again theoretically, but no data regarding clinical response after a "second line" of treatment with the same biologic are available. The question of optimal treatment duration is also questioned with other biologics.
The costs related to OMA are high (estimated to 12 k€/year/patient). Frequent injections (1 subcutaneous injection every 4 weeks for the lowest dose to 4 injections every 2 weeks for the highest dose) represent severe constraints for patients, especially for the youngest ones. For all these reasons, evaluating whether shortening duration of OMA therapy is feasible while maintaining acceptable asthma control is a critical point. The main objective is to demonstrate the non-inferiority (i.e. no more exacerbations at 12 months) of OMA withdrawal attempt compared to OMA continuation in asthma-controlled patients treated for at least 33 months with OMA. Secondary objectives are to compare OMA withdrawal attempt versus OMA continuation in asthma-controlled patients treated for at least 33 months with OMA on other asthma control features at 6 and 12 months.
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
- None
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
- •Adult patient >18 years old
- •Treated with OMA, prescribed by a pulmonologist , for at least 33 months for severe allergic asthma
- •Well controlled with the treatment (ACT score ⩾ 18) and having experienced no more than one exacerbation in the year preceding inclusion. An exacerbation is defined as an oral or injectable steroid course for at least 2 days and/or a minimum doubling of the usual steroid dose for at least 2 days for steroid dependent patients
排除标准
- •Patient refusing to stop OMA treatment, whatever the reason
- •Patient with other reason other than good asthma control to stop OMA, such as a side effect, planned or ongoing pregnancy, or planned switch to another step 5 asthma treatment (mepolizumab, benralizumab, dupilumab, reslizumab, daily oral steroids, bronchial thermoplasty, ...)
- •Patient not covered by Health Insurance
- •Patient under curatorship, guardianship or safeguarding of justice
- •Patient whose adherence to asthma treatments is considered poor or questionable by the investigator
- •Patient participating in another intervention research
- •Pregnant or lactating patient
- •Patient refusing to sign consent
研究组 & 干预措施
OMA withdrawal attempt
Patients will be told to stop abruptly (no progressive decrease of the dose) their Omalizumab treatment and they will not be prescribed new OMA
干预措施: Attempt to withdrawal OMA treatment (Other)
OMA continuation
Patients will be prescribed the same dosage of Omalizumab than they received before randomization
干预措施: Continuation of OMA treatment (Drug)
结局指标
主要结局
Number of exacerbations
时间窗: 12 months
Number of asthma exacerbations in the year following randomization. An exacerbation is defined as an oral or injectable steroid course for at least 2 days and/or a minimum doubling of the usual steroid dose for at least 2 days for steroid dependent patients. They will be assessed every 6 months from patients log book, written reports of ER visits or hospitalizations, and prescriptions
次要结局
- Time to exacerbation(12 months)
- Asthma control (ACT)(12 months)
- 5 points-decrease of asthma control (ACT)(12 months)
- Time to loss of asthma control(12 months)
- Asthma quality of life (AQLQ)(12 months)
- Number of asthma controller drugs(12 months)
- Dose of inhaled steroids(12 months)
- Dose of oral steroids(12 months)
- Patients increasing their dose of oral steroids of 20%(12 months)
- Patients increasing their dose of oral steroids of 50%(12 months)
- Patients increasing their dose of oral steroids of 80%(12 months)
- Allergy manifestations(12 months)
- FEV1(12 months)
- Effect of OMA treatment duration on asthma control(12 months)
- Effect of OMA dosage on asthma control(12 months)
- Effect of eosinophils rate on asthma control(12 months)
- Effect of OMA treatment duration on time to loss of asthma control(12 months)
- Effect of OMA dosage on time to loss of asthma control(12 months)
- Effect of eosinophils rate on time to loss of asthma control(12 months)
- Effect of OMA treatment duration on exacerbations(12 months)
- Effect of OMA dosage on exacerbations(12 months)
- Effect of eosinophils rate on exacerbations(12 months)
- Hospitalisation for asthma(12 months)
- Emergency room visits for asthma(12 months)
- St. George's Respiratory Questionnaire (SGRQ)(12 months)
