Azole-echinocandin Combination Therapy for Invasive Aspergillosis (IA-DUET)
Azole-echinocandin Combination Therapy for Invasive Aspergillosis A Randomized Pragmatic Superiority Trial
The goals of this study are 3-fold:
First, the main study and the primary endpoint will evaluate if the overall mortality can be decreased with initial azole-echinocandin combination therapy compared with triazole monotherapy in patients with IA and documented voriconazole susceptibility.
Second, the study design described will also allow to study several other subpopulations; Indeed, the outcome of the following subgroups will be evaluated as well; a. Patients starting azole monotherapy but who switch to directed therapy when it has become clear that the infection is caused by an azole resistant A. fumigatus. b. patients in which eventually no resistance data become available in relation to the treatment they received.
Third, the study will evaluate what the outcome is of patients that turn out to be infected with a triazole resistant A. fumigatus who started with a triazole-echinocandin combination therapy.
研究概览
详细说明
Background of the study:
Patients with underlying haematological malignancies or immunocompromised for various other reasons, are prone to fungal infections. Invasive aspergillosis (IA) is a common complication during remission inducing chemotherapy for acute leukemia or other hematological malignancies, as well as those who have undergone allogeneic hematopoietic stem cell transplantation (HSCT) or solid organ transplantation (SOT).
For more than 15 years voriconazole, a drug of the triazole class, has been the recommended treatment for this life-threatening infection after a pivotal randomized trial showed an improved survival with voriconazole compared with amphotericin B deoxycholate. However, also with voriconazole the overall 6-week mortality is still unacceptably high at 25-30%.
Therefore, a randomized controlled trial assed the efficacy of voriconazole with or without anidulafungin for the treatment of IA in haematology patients to prove that combination therapy can improve outcome.Among the 277 patients with IA in this study, the 6-week mortality with combination therapy was 30% lower (19.3%) than with monotherapy (27.5%), p=0.087. In a post-hoc analysis of the 222 patients with radiographic abnormalities and a positive galactomannan antigen test, a statistically significant difference in mortality was observed (p=0.037). Though, this study did not result in conclusive evidence in favor of combination therapy, it is a credible study which adds to the already existing in vitro and animal studies in support of echinocandin triazole combination therapy for IA and thus paves the way for a second larger and pragmatic clinical trial. Another important and new consideration about the management of IA is the upcoming of infections with triazole-resistant A. fumigatus. This is increasingly becoming a worldwide problem and leads to longer hospital stay, higher costs and is associated with a very high mortality.
It is very likely that the excessive use of antifungals of the triazole class in agriculture has formed the basis of this problem.
Since 2018 the Dutch Working Party on Antibiotic therapy (SWAB) guideline on the management of invasive fungal infections therefore recommends upfront combination therapy (azole plus echinocandins or liposomal-amfotericine B) until resistance can be excluded as one of the treatment options for IA. Given the evidence in favor of voriconazole-echinocandin combination therapy as well as the increasing incidence of voriconazoleresistant A. fumigatus in Belgium and the Netherlands, a large clinical study on the value of combination therapy is urgently needed.
Objective of the study:
Primary objective
1. Evaluate if the survival in patients with a triazole susceptible IA can be improved when the initial therapy consists of triazole and echinocandin combination therapy instead of triazole monotherapy.
Secondary objectives
- Evaluate if a triazole/echinocandin combination therapy improves the overall quality of life and if it is a cost-effective intervention
- Evaluate the outcome of patients in which a triazole-resistant A. fumigatus is detected in relation to the initial antifungal therapy patients had received (i.e. triazole monotherapy or combination therapy).
- Evaluate the outcome of patients in which resistance testing is unsuccessful in function of the antifungal therapy they received.
- Evaluate if the baseline serum galactomannan value and the serum galactomannan kinetics are predictive of overall 6-week survival.
Study design:
A non-blinded phase 3 randomized pragmatic clinical trial.
Study population:
Immunocompromised patients who fulfill the EORTC/MSG host factor and mycological criteria of invasive aspergillosis ICU patients with influenza who fulfill a definition of IA specific for this population
Intervention:
Treatment with a triazole (voriconazole or isavuconazole or posaconazole) + anidulafungin IV. The triazole is administered for at least 6 weeks while anidulafungin is given for at least 7 and a maximum of 28 days.
Comparator:
Treatment with a triazole (voriconazole or isavuconazole or posaconazole) for at least 6 weeks.
研究类型
注册 (预期的)
阶段
- 第三阶段
联系人和位置
学习联系方式
- 姓名：Bart Rijnders, MD, PhD
- 电话号码：+31107033510
- 邮箱：b.rijnders@erasmusmc.nl
研究联系人备份
- 姓名：Sammy Huygens
- 邮箱：s.huygens@erasmusmc.nl
学习地点
-
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Ghent、比利时
- 招聘中
- UZ Ghent
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接触：
- Alexander Schauwvlieghe, MD
- 邮箱：Alexander.Schauwvlieghe@uzgent.be
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Leuven、比利时
- 招聘中
- UZ Leuven
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接触：
- Johan Maertens, MD
- 邮箱：johan.maertens@uzleuven.be
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接触：
- Robina Aerts, MD
- 邮箱：robina.aerts@uzleuven.be
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Nijmegen、荷兰
- 尚未招聘
- Radboud Universitair Medisch Centrum
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接触：
- N. Blijlevens
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Zuid Holland
-
Rotterdam、Zuid Holland、荷兰、3000 CA
- 招聘中
- Erasmus Medical Center (EMC)
-
接触：
- Bart J Rijnders, MD, PhD
- 电话号码：31107033510
- 邮箱：b.rijnders@erasmusmc.nl
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-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- 18 years or older
- Have started or will start voriconazole or isavuconazole (or posaconazole if voriconazole or isavuconazole cannot be given as per treating physician's decision) as antifungal therapy on the baseline visit.
- For all patients: presence of one of the EORTC/MSG host factors as defined in appendix 1 or being admitted to the ICU with influenza
- For non-ICU patients or ICU patients without influenza: Meet the EORTC/MSG clinical criterium (appendix 1)
- For non-ICU patients or ICU patients without influenza: Meet the mycological criterium (appendix 1) or fulfil inclusion criterium 7
- For ICU patients with influenza we consider an isolated positive sputum culture for Aspergillus spp. insufficient as amycological criterium. Therefore, in these patients only one of the following mycological criteria are acceptable; Serum galactomannan ≥0.5, BAL galactomannan ≥1.0 or Aspergillus spp. cultured in BAL fluid.
- Please note that patients with AML receiving chemotherapy or patients with ALL receiving or having received corticosteroid therapy within the last 4 weeks in the context of their pre-phase, induction, consolidation, intensification or interphase treatment as well as patients receiving systemic immunosuppressive therapy for GVHD can be included before the mycological criterium is fulfilled on condition that they fulfill the EORTC/MSG lung CT radiology criteria (halo sign, well-described nodule, cavity as described in appendix 1) at the time of inclusion and as long as the mycological test results are expected to become available within 96 and no later than 7 days after inclusion. If these test results turn out to be negative, the patient will be withdrawn from the study and further treatment is at physician's discretion.
- Written informed consent by patient or legal representative.
Exclusion Criteria:
- Known history of allergy, hypersensitivity or serious reaction to azole or echinocandin antifungals;
- Patients with chronic invasive aspergillosis or a chronic non-invasive aspergillus infection (e.g. aspergilloma) defined as the clinical or radiological sign of infection being present for >28 days.
- Receipt of itraconazole, voriconazole, posaconazole or isavuconazole as prophylaxis for at least 7 days in the 14 days preceding the date of the first radiological signs of the Aspergillus infection. Patients in which the most recent serum level of the triazole given as prophylaxis was subtherapeutic can be included (*).
- Receipt of echinocandin prophylaxis for >96 hours in the preceding 7 days
- Receipt of systemic antifungal treatment with an echinocandin or an azole for the current episode of invasive aspergillosis for a duration of > 96 hours.
- For patients in the Netherlands only: Diagnostic testing to exclude azole resistance will not be possible (sputum cultures are negative and BAL sampling will not be performed)
- ICU patients only: Patients with a sequential organ failure assessment (SOFA) score >11 at the time of screening for the study are excluded. If randomization is done >24 hours after screening the calculation should be repeated before the patient can be randomized (appendix 3)
- ICU patients only: Patients in which weaning from the ventilator or ECMO system is deemed unlikely due to irreversible lung damage
- Patients with any condition which, in the opinion of the investigator, could affect patient safety, preclude evaluation of response (e.g. because survival beyond 6 weeks is unlikely due to the underlying disease status)
- Patient previously included in this study
学习计划
研究是如何设计的？
设计细节
- 主要用途：治疗
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器：Azole monotherapy
Azole monotherapy Voriconazole or isavuconazole or posaconazole will be dosed according to the SPC and according to the route of administration (IV or orally) that is preferred by the treating physician. However, the dose may be changed based on therapeutic drug monitoring levels according to the local standard of care. |
Dosing according to the SPC
其他名称：
|
|
实验性的：Azole + Anidulafungin
Azole + Anidulafungin Voriconazole or isavuconazole or posaconazole will be dosed according to the SPC and according to the route of administration (IV or orally) that is preferred by the treating physician. However, the dose may be changed based on therapeutic drug monitoring levels according to the local standard of care. Anidulafungin (Ecalta) is available as an intravenous formulation only. It will be used at the licensed dose of a 200mg loading dose on day 1 and 100mg QD thereafter. No dose adjustment is needed in patients with renal or hepatic insufficiency of any grade. |
Dosing according to the SPC
其他名称：
200mg loading dose on day 1 and 100mg QD thereafter
其他名称：
|
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Overall survival 42 days
大体时间：42 days after the start of antifungal therapy
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Overall survival 42 days after the start of antifungal therapy in the MITT population
|
42 days after the start of antifungal therapy
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Overall aspergillus attributable mortality
大体时间：12 weeks after the start of antifungal therapy
|
Overall aspergillus attributable mortality 12 weeks after the start of antifungal therapy.
|
12 weeks after the start of antifungal therapy
|
|
Overall survival 12 weeks
大体时间：12 weeks after the start of antifungal therapy
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Overall survival 12 weeks after the start of antifungal therapy in the MITT population
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12 weeks after the start of antifungal therapy
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Overall survival 6 weeks (subgroup with positive serum galactomannan at baseline)
大体时间：6 weeks after the start of therapy
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Overall survival 6 weeks after the start of therapy in the subgroup of patients in the MITT population with a positive serum galactomannan test at baseline.
|
6 weeks after the start of therapy
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|
Overall survival 6 weeks (subgroup non-ICU patients who fulfill the EORTC/MSG probable or proven definition)
大体时间：6 weeks after the start of therapy
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Overall survival 6 weeks after the start of therapy in the subgroup of non-ICU patients who fulfill the EORTC/MSG probable or proven definition (MITT population).
|
6 weeks after the start of therapy
|
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Overall survival 6 weeks (subgroup of non-ICU patients with an underlying haematological disease (MITT population))
大体时间：6 weeks after the start of therapy
|
Overall survival 6 weeks after the start of therapy in the subgroup of non-ICU patients with an underlying haematological disease (MITT population)
|
6 weeks after the start of therapy
|
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Overall survival 6 weeks (subgroup of non-ICU patients without an underlying haematological disease (MITT population))
大体时间：6 weeks after the start of therapy
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Overall survival 6 weeks after the start of therapy in the subgroup of non-ICU patients without an underlying haematological disease (MITT population)
|
6 weeks after the start of therapy
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Overall survival 6 weeks in patients that started with triazole monotherapy and in which triazole resistance is detected during follow-up (MITT population)
大体时间：6 weeks after the start of therapy
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Overall survival 6 weeks after the start of therapy in patients that started with triazole monotherapy and in which triazole resistance is detected during follow-up (MITT population)
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6 weeks after the start of therapy
|
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Overall survival 6 weeks after the start of therapy in patients that started with triazole-anidulafungin combination therapy and in which triazole resistance is detected during follow-up (MITT population)
大体时间：6 weeks after the start of therapy
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Overall survival 6 weeks after the start of therapy in patients that started with triazole-anidulafungin combination therapy and in which triazole resistance is detected during follow-up (MITT population)
|
6 weeks after the start of therapy
|
|
Kinetics of serum galactomannan levels
大体时间：6 weeks after the start of therapy
|
In the subgroup of patients with a positive serum galactomannan; Kinetics of serum galactomannan levels with combination versus monotherapy
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6 weeks after the start of therapy
|
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Mortality of patients in which resistance testing was unsuccessful
大体时间：12 weeks after the start of therapy
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Mortality of patients in which resistance testing was unsuccessful
|
12 weeks after the start of therapy
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Time to hospital discharge
大体时间：24 weeks after the start of therapy
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Time to hospital discharge (in the MITT subgroup of patients admitted to the hospital at baseline)
|
24 weeks after the start of therapy
|
合作者和调查者
合作者
调查人员
- 首席研究员：Bart Rijnders, MD, PhD、Erasmus Medical Center
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (预期的)
研究完成 (预期的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- NL72950.078.20
- 2020-000627-40 (EudraCT编号)
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