Unravelling Targets of Therapy in Bronchial Thermoplasty in Severe Asthma

Asthma Clinical Trial

— TASMA  

Official title:

Unravelling Targets of Therapy in Bronchial Thermoplasty in Severe Asthma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02225392
• Other study ID #: NL45394.018.13
• Secondary ID: 5.2.13.064907134
• Status: Completed
• Phase: N/A
• Start date: April 2014
• Est. completion date: December 2019

Study information

• Verified date: December 2022
• Source: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Approximately 5% of asthma patients suffer from severe asthma that is characterized by frequent asthma exacerbations resulting in significant morbidity and excessive utilisation of health care resources. Therefore, there is a strong need for improved therapeutic strategies for these patients. Insight in the pathogenesis and molecular pathways active in severe asthma is crucial to reach this goal.

Bronchial Thermoplasty (BT) is a novel, innovative device-based treatment of severe asthma that is based on local, radiofrequent energy delivery in larger airways during bronchoscopy.

Hypothesis:

BT-induced clinical improvement in severe asthma is a consequence of reduction in airway smooth muscle (ASM) mass and (contractile/immunomodulatory) function, inflammation, neural innervation and/or vascular integrity resulting in altered airway remodelling. BT target identification and severe asthma phenotyping are critical for improved patient selection for BT and fundamental to discover novel, specific signalling pathways active in severe asthma.

Description:

This study has a two-fold purpose:

1. to unravel the targets of BT in severe asthma (how does it work?) which is fundamental for better patient selection (who benefits most?) and further improvement of BT technology and novel asthma therapy development (how to treat better?). These objectives can only be achieved by linking patient-reported outcomes to airway structure/function, which is the principal aim of the study proposed.

2. to investigate clinical outcome analyses

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: December 2019
• Est. primary completion date: December 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Males or females age 18 or greater and 65 or less

2. The diagnosis of asthma confirmed by at least one of the following as assessed at least once during the past 5 years before the study:

• Reversibility to ß2-agonists =12% predicted and =200ml after 400µg inhaled salbutamol or equivalent

• Bronchial hyper-responsiveness to methacholine or histamine

• Peak-flow variability of >20% over a period of 14 days

• Fall in FEV1 >12% and >200ml when tapering treatment (ICS, oral steroid, LABA and/or LTRA).

3. Subject is taking regular maintenance medication (GINA step 4-5) for past 6 months that includes:

• Inhaled corticosteroid at a dosage =500µg fluticasone equivalent per day AND

• Long acting ß2-agonist at a dosage of =100µg per day salmeterol dose aerosol or equivalent).

4. Per protocol bronchial hyper-responsiveness to methacholine (PC20<4 mg/ml)

5. Other asthma medications are acceptable (such as Leukotriene modifiers, Theophylline, Omalizumab treatment (or discontinuation for at least 6 months) Systemic corticosteroid use (=20mg/day prednisone equivalent))

6. Pre-bronchodilator FEV1 =50% predicted (stabilized on ICS/LABA) and post-bronchodilator FEV1 =60%

7. ACQ >1,5 for 2 weeks

8. Non-smoker for 1 year or more (former smoker =15 pack years)

9. Ability to undergo bronchoscopy and BT in the opinion of the investigator.

10. Ability and willingness to provide informed consent.

11. For women of childbearing potential: non pregnant, non-lactating, and agree to practice an adequate birth control method for the duration of the study.

Exclusion Criteria:

1. Asthma exacerbation during the prior 4 weeks.

2. Subject has 5 or more hospitalizations for exacerbations of asthma in the previous year or 1 or more ICU admission for mechanical or endotracheal intubation for asthma in the previous year.

3. Respiratory tract infection within past 4 weeks

4. Subject has a known sensitivity to medications required to perform bronchoscopy

5. Subject is using immunosuppressant therapy other than oral steroid therapy

6. Subject is on anticoagulant medication including anti-platelet agents.

7. Subject has bleeding diathesis, platelet dysfunction, thrombocytopenia with platelet count less than 125,000/mm2 or known coagulopathy (INR >1.5).

8. Subject has other respiratory diseases including interstitial lung disease, emphysema, cystic fibrosis, mechanical upper airway obstruction, Churg-Strauss syndrome, and allergic bronchopulmonary aspergillosis (total IgE of >1000 Units/mL with positive specific IgE to aspergillus and evidence of central bronchiectasis).

9. Subject has segmental atelectasis, lobar consolidation, significant or unstable pulmonary infiltrate, or pneumothorax, confirmed on x-ray. Bronchiectasis on HR-CT-of the chest, both centrally or peripherally will be excluded.

10. Subject has clinically significant cardiovascular disease, including myocardial infarction, angina, cardiac dysrhythmia, conduction defect, cardiomyopathy, aortic aneurysm, or stroke at the discretion of the investigator

11. Subject has uncontrolled hypertension (>200mmHg systolic or >100mmHg diastolic pressure).

12. Subject uses an internal or external pacemaker or cardiac defibrillator.

13. Other chronic diseases that in the opinion of the investigator would prevent participation in the trial or put the participant at risk by participation, e.g. liver, kidney, or nervous system

14. Current smokers, and a history of cigarette smoking with >15 pack years total

15. Use of investigative drugs or intervention trials in the 4 months prior to enrolment or during the duration of the study

16. Any condition or compliance issue which in the opinion of the investigator might interfere with participation inthe study

17. BMI >35

18. Pre-bronchodilator FEV1 <1.2L

19. Extreme coughing

Related Conditions & MeSH terms

• Asthma
• Bronchial Asthma

Intervention

Procedure:
• Bronchial thermoplasty
Bronchial thermoplasty (BT) will be performed using the Alair system (Boston Scientific, USA). Patients will undergo 3 bronchoscopy procedures with BT at least 3 weeks apart. Treatment sessions are designed to address different lobes of the lung with the right lower lobe treated during the first bronchoscopy, the left lower lobe treated during the second bronchoscopy, and both the right and left upper lobes treated in the third and final bronchoscopy. The right middle lobe and proximal airways including RC2 are left untreated.

Device:
• Alair system (Boston Scientific, USA)
The alair system consist of a controller and a bastket catheter.

Locations

Country	Name	City	State
Netherlands	Academisch Medisch Centrum	Amsterdam	Noord Holland
Netherlands	University Medical Center Groningen	Groningen
United Kingdom	Royal Brompton Hospital	London

Sponsors (4)

Lead Sponsor	Collaborator
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)	Boston Scientific Corporation, The Netherlands Asthma Foundation, ZonMw: The Netherlands Organisation for Health Research and Development

Countries where clinical trial is conducted

Netherlands,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	The change in Airway-resistance (sRaw)/-conductance(sGaw)/-mechanics (forced oscillation technique (FOT)) parameters after bronchial thermoplasty treatment		Baseline, 24 weeks
Other	The change in exhaled volatile organic compounds (VOCs) after bronchial thermoplasty treatment		Baseline, 24 weeks
Primary	The change in airway smooth muscle (ASM) mass between immediate BT treated and the control group (N=20, randomized)	The change in ASM mass as determined by the percentage of ASM surface area in airway biopsies between: the immediate BT group and; the delayed BT group = control group	Baseline, week 25
Secondary	The change in ASM mass in airway biopsies before and after bronchial thermoplasty treatment (N=40, observational, before and after BT)	Change in ASM mass in endobronchial biopsies before and after bronchial thermoplasty treatment	Baseline, 25 weeks
Secondary	The change in structural airway remodelling after and during bronchial thermoplasty treatment	Optical Coherence Tomography (OCT)- and/or Radial Endobronchial ultrasound (rEBUS)-determined changes in structural airway remodelling.	Baseline, week 25
Secondary	The change in pre-and post bronchodilator FEV1 and related % reversibility between immediate BT treated and control group (N=20, randomized)		Baseline, 24 week
Secondary	The change in PC20 methacholine between immediate BT treated and control group (N=20, randomized)		Baseline, 24 week
Secondary	The change in Fraction of exhaled nitric oxide (FeNO) between immediate BT treated and control group (N=20, randomized)		Baseline, 24 week
Secondary	The change in asthma control questionnaire (ACQ) between immediate BT treated and control group (N=20, randomized)		Baseline, 24 week
Secondary	The change in - asthma related quality of life questionnaire (AQLQ) between immediate BT treated and control group (N=20, randomized)		Baseline, 24 week
Secondary	The change in health care utilization between immediate BT treated and control group (N=20, randomized)		Baseline, 24 week
Secondary	The change in rescue medication use between immediate BT treated and control group (N=20, randomized)		Baseline, 24 week
Secondary	The change in inflammatory cell density/counts in biopsy, BAL and induced sputum between immediate BT treated and control group (N=20, randomized)		Baseline, 25 week
Secondary	The change in pre-and post bronchodilator FEV1 and related % reversibility after bronchial thermoplasty treatment (N=40, observational, before and after BT)		Baseline, 24 week
Secondary	The change in PC20 methacholine after bronchial thermoplasty treatment (N=40, observational, before and after BT)		Baseline, 24 week
Secondary	The change in Fraction of exhaled nitric oxide (FeNO) after bronchial thermoplasty treatment (N=40, observational, before and after BT)		Baseline, 24 week
Secondary	The change in asthma control questionnaire (ACQ) after bronchial thermoplasty treatment (N=40, observational, before and after BT)		Baseline, 24 week
Secondary	The change in asthma related quality of life questionnaire (AQLQ) after bronchial thermoplasty treatment (N=40, observational, before and after BT)		Baseline, 24 week
Secondary	The change in health care utilization after bronchial thermoplasty treatment (N=40, observational, before and after BT)		Baseline, 24 week
Secondary	The change in rescue medication use after bronchial thermoplasty treatment (N=40, observational, before and after BT)		Baseline, 24 week
Secondary	The change in inflammatory cell density/counts in biopsy, BAL and induced sputum before and after bronchial thermoplasty treatment (N=40, observational, before and after BT)		Baseline, 25 week