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Efficacy of Azithromycin to Prevent Bronchiolitis Obliterans Syndrome After Allogeneic Hematopoietic Stem Cell Transplantation (ALLOZITHRO)

Primary Purpose

Malignant Hematological Diseases

Status
Unknown status
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Azithromycin
Placebo
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Malignant Hematological Diseases focused on measuring hematopoietic stem cell transplantation, pulmonary non-infectious complications, bronchiolitis obliterans syndrome

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients> 16 years old
  • Experimenting an allogeneic HSCT for a hematologic malignancy
  • Pre-transplantation Pulmonary Function Testing
  • With written informed consent

Exclusion Criteria:

  • Allergy or Intolerance to azithromycin, macrolides or ketolide or excipient
  • Prolonged corrected QT (QTc) interval (>450 msec)
  • Taking medications that prolong the QTc interval (Cisapride, ergotamine, dyhydroergotamine)
  • Taking ergotamine and dyhydroergotamine due to the risk of ergotism
  • Family history of a prolonged QTc interval.
  • History of congestive heart failure
  • Taking colchicine Severe liver insufficiency • History of infection due to atypical mycobacteria

Sites / Locations

  • Saint Louis

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Azithromycine

Placebo

Arm Description

250 mg x 3/week during a meal for a period of 2 years

250 mg x 3/week during a meal for a period of 2 years.

Outcomes

Primary Outcome Measures

Airflow decline (AFD)-free survival
Defined on the criteria from Chien JW et al (Am J Resp Crit Care Med 2003;168:208-14) by an annualized decline of percent predicted forced expiratory volume in 1 second (FEV1) of more than 5%

Secondary Outcome Measures

Overall survival
Occurrence of late-onset pulmonary non-infectious complications (=bronchiolitis obliterans syndrome, SBO)
bronchiolitis obliterans syndrome (SBO) is defined as the absence of infection with an forced expiratory volume in 1 second (FEV1) of <75% of predicted or a decline of > 10% and FEV1/Slow vital capacity (SVC) < 0.7 or residual volume (RV) or RV/total lung capacity (TLC) > 120%, and interstitial lung disease, which is defined as the onset of new interstitial lung abnormalities observed with a lung CT scan and the absence of infection.
Variation of pulmonary function testing parameters
variation in mean forced expiratory volume in 1 second (FEV1) decline, forced vital capacity (FVC), residual volume (RV), Total Lung capacity (TLC), Forced expiratory flow at 25% point to the 75% point of Forced Vital Capacity (FEF25-75%) as compared to baseline values (at inclusion)
Occurrence of acute and chronic extra-thoracic graft versus host disease (GVHD)
Cumulative incidence of hematological relapse
Quality of life
Tolerance
adverse events
Cumulative dose of steroids treatment

Full Information

First Posted
October 7, 2013
Last Updated
January 6, 2020
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT01959100
Brief Title
Efficacy of Azithromycin to Prevent Bronchiolitis Obliterans Syndrome After Allogeneic Hematopoietic Stem Cell Transplantation
Acronym
ALLOZITHRO
Official Title
Evaluation of the Efficacy of Azithromycin to Prevent Bronchiolitis Obliterans Syndrome After Allogeneic Hematopoietic Stem Cell Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Unknown status
Study Start Date
February 2014 (undefined)
Primary Completion Date
April 2017 (Actual)
Study Completion Date
August 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The occurrence of bronchiolitis obliterans syndrome (SBO) after allogeneic hematopoietic stem cell transplantation (HSCT) is considered to be a chronic pulmonary graft versus host disease (GVHD) that is associated with significant mortality and morbidity. The reported incidence of SBO varies from 6 to 26% of allogeneic HSC recipients and is usually diagnosed within 2 years after transplantation. The diagnosis of SBO relies on the occurrence of a new airflow obstruction identified during pulmonary function testing, and the definition differs between studies. Currently, no curative immunosuppressive treatment is available, and recent data suggest that the use of these treatments, especially corticosteroids, should be limited because of their toxicity. The impairment of lung function parameters is likely caused by fibrous small airway lesions. Few data on the pathogenesis of SBO after allogeneic HSCT are available. Several hypotheses are based on the occurrence of SBO during chronic graft rejection after lung transplantation, which shares many clinical and histopathological similarities with SBO after allogeneic HSCT. One hypothesis is that the first step leading to SBO is lung epithelium injury. SBO is then identified as an alloimmune reaction with only one clearly identified risk factor: extrathoracic chronic GVHD. Due to their anti-inflammatory and immunomodulatory properties, recent data suggest that low-dose macrolides may be effective at preventing SBO after lung transplants. This well-tolerated treatment may be useful for preventing SBO after allogeneic HSCT. The objective of this Phase 3 multicentre randomized, double-blinded, clinical trial is to evaluate the efficacy of azithromycin in preventing BO syndrome after allogeneic HSCT in patients with malignant hematological diseases.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malignant Hematological Diseases
Keywords
hematopoietic stem cell transplantation, pulmonary non-infectious complications, bronchiolitis obliterans syndrome

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
480 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Azithromycine
Arm Type
Experimental
Arm Description
250 mg x 3/week during a meal for a period of 2 years
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
250 mg x 3/week during a meal for a period of 2 years.
Intervention Type
Drug
Intervention Name(s)
Azithromycin
Intervention Description
250 mg x 3/week per os during a meal for a period of 2 years
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
250 mg x 3/week during a meal for a period of 2 years
Primary Outcome Measure Information:
Title
Airflow decline (AFD)-free survival
Description
Defined on the criteria from Chien JW et al (Am J Resp Crit Care Med 2003;168:208-14) by an annualized decline of percent predicted forced expiratory volume in 1 second (FEV1) of more than 5%
Time Frame
2 year after allogeneic HSCT
Secondary Outcome Measure Information:
Title
Overall survival
Time Frame
within 2 years of inclusion
Title
Occurrence of late-onset pulmonary non-infectious complications (=bronchiolitis obliterans syndrome, SBO)
Description
bronchiolitis obliterans syndrome (SBO) is defined as the absence of infection with an forced expiratory volume in 1 second (FEV1) of <75% of predicted or a decline of > 10% and FEV1/Slow vital capacity (SVC) < 0.7 or residual volume (RV) or RV/total lung capacity (TLC) > 120%, and interstitial lung disease, which is defined as the onset of new interstitial lung abnormalities observed with a lung CT scan and the absence of infection.
Time Frame
within 2 years after inclusion
Title
Variation of pulmonary function testing parameters
Description
variation in mean forced expiratory volume in 1 second (FEV1) decline, forced vital capacity (FVC), residual volume (RV), Total Lung capacity (TLC), Forced expiratory flow at 25% point to the 75% point of Forced Vital Capacity (FEF25-75%) as compared to baseline values (at inclusion)
Time Frame
within 2 years after inclusion
Title
Occurrence of acute and chronic extra-thoracic graft versus host disease (GVHD)
Time Frame
within 2 years after inclusion
Title
Cumulative incidence of hematological relapse
Time Frame
within the 2 years after inclusion
Title
Quality of life
Time Frame
within 2 years after inclusion
Title
Tolerance
Description
adverse events
Time Frame
within 2 years of inclusion
Title
Cumulative dose of steroids treatment
Time Frame
within the 2 years after inclusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients> 16 years old Experimenting an allogeneic HSCT for a hematologic malignancy Pre-transplantation Pulmonary Function Testing With written informed consent Exclusion Criteria: Allergy or Intolerance to azithromycin, macrolides or ketolide or excipient Prolonged corrected QT (QTc) interval (>450 msec) Taking medications that prolong the QTc interval (Cisapride, ergotamine, dyhydroergotamine) Taking ergotamine and dyhydroergotamine due to the risk of ergotism Family history of a prolonged QTc interval. History of congestive heart failure Taking colchicine Severe liver insufficiency • History of infection due to atypical mycobacteria
Facility Information:
Facility Name
Saint Louis
City
Paris
State/Province
Ile De France
ZIP/Postal Code
75010
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
25835160
Citation
Bergeron A, Chevret S, Chagnon K, Godet C, Bergot E, Peffault de Latour R, Dominique S, de Revel T, Juvin K, Maillard N, Reman O, Contentin N, Robin M, Buzyn A, Socie G, Tazi A. Budesonide/Formoterol for bronchiolitis obliterans after hematopoietic stem cell transplantation. Am J Respir Crit Care Med. 2015 Jun 1;191(11):1242-9. doi: 10.1164/rccm.201410-1818OC.
Results Reference
result
PubMed Identifier
28787506
Citation
Bergeron A, Chevret S, Granata A, Chevallier P, Vincent L, Huynh A, Tabrizi R, Labussiere-Wallet H, Bernard M, Chantepie S, Bay JO, Thiebaut-Bertrand A, Thepot S, Contentin N, Fornecker LM, Maillard N, Risso K, Berceanu A, Blaise D, Peffault de La Tour R, Chien JW, Coiteux V, Socie G; ALLOZITHRO Study Investigators. Effect of Azithromycin on Airflow Decline-Free Survival After Allogeneic Hematopoietic Stem Cell Transplant: The ALLOZITHRO Randomized Clinical Trial. JAMA. 2017 Aug 8;318(6):557-566. doi: 10.1001/jama.2017.9938.
Results Reference
derived

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Efficacy of Azithromycin to Prevent Bronchiolitis Obliterans Syndrome After Allogeneic Hematopoietic Stem Cell Transplantation

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