Science and Research

Amikacin Liposome Inhalation Suspension for Treatment-Refractory Lung Disease Caused by Mycobacterium avium Complex (CONVERT). A Prospective, Open-Label, Randomized Study

Rationale: Improved therapeutic options are needed for patients with treatment-refractory nontuberculous mycobacterial lung disease caused by Mycobacterium avium complex (MAC). Objectives: To evaluate the efficacy and safety of daily amikacin liposome inhalation suspension (ALIS) added to standard guideline-based therapy (GBT) in patients with refractory MAC lung disease. Methods: Adults with amikacin-susceptible MAC lung disease and MAC-positive sputum cultures despite at least 6 months of stable GBT were randomly assigned (2:1) to receive ALIS with GBT (ALIS + GBT) or GBT alone. Once-daily ALIS was supplied in single-use vials delivering 590 mg amikacin to the nebulizer. The primary endpoint was culture conversion, defined as three consecutive monthly MAC-negative sputum cultures by Month 6. Measurements and Main Results: Enrolled patients (ALIS + GBT, n = 224; GBT-alone, n = 112) were a mean 64.7 years old and 69.3% female. Most had underlying bronchiectasis (62.5%), chronic obstructive pulmonary disease (14.3%), or both (11.9%). Culture conversion was achieved by 65 of 224 patients (29.0%) with ALIS + GBT and 10 of 112 (8.9%) with GBT alone (odds ratio, 4.22; 95% confidence interval, 2.08-8.57; P < 0.001). Patients in the ALIS + GBT arm versus GBT alone were more likely to achieve conversion (hazard ratio, 3.90; 95% confidence interval, 2.00-7.60). Respiratory adverse events (primarily dysphonia, cough, and dyspnea) were reported in 87.4% of patients receiving ALIS + GBT and 50.0% receiving GBT alone; serious treatment-emergent adverse events occurred in 20.2% and 17.9% of patients, respectively. Conclusions: Addition of ALIS to GBT for treatment-refractory MAC lung disease achieved significantly greater culture conversion by Month 6 than GBT alone, with comparable rates of serious adverse events. Clinical trial registered with www.clinicaltrials.gov (NCT02344004).
  • Griffith, D. E.
  • Eagle, G.
  • Thomson, R.
  • Aksamit, T. R.
  • Hasegawa, N.
  • Morimoto, K.
  • Addrizzo-Harris, D. J.
  • O'Donnell, A. E.
  • Marras, T. K.
  • Flume, P. A.
  • Loebinger, M. R.
  • Morgan, L.
  • Codecasa, L. R.
  • Hill, A. T.
  • Ruoss, S. J.
  • Yim, J. J.
  • Ringshausen, F. C.
  • Field, S. K.
  • Philley, J. V.
  • Wallace, R. J., Jr.
  • van Ingen, J.
  • Coulter, C.
  • Nezamis, J.
  • Winthrop, K. L.
  • Convert Study Group

Keywords

  • Administration, Inhalation
  • Amikacin/administration & dosage/*therapeutic use
  • Anti-Bacterial Agents/administration & dosage/*therapeutic use
  • Female
  • Humans
  • Liposomes
  • Lung Diseases/*drug therapy/microbiology
  • Male
  • Middle Aged
  • Mycobacterium avium Complex
  • Mycobacterium avium-intracellulare Infection/*drug therapy
  • Prospective Studies
  • Treatment Outcome
  • *alis
  • *culture conversion
  • *guideline-based therapy
  • *liposomal amikacin for inhalation
  • *nontuberculous mycobacteria
Publication details
DOI: 10.1164/rccm.201807-1318OC
Journal: Am J Respir Crit Care Med
Pages: 1559-1569 
Number: 12
Work Type: Original
Location: BREATH
Disease Area: General Lung and Other
Partner / Member: MHH
Access-Number: 30216086
See publication on PubMed

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