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Amikacin Liposome Inhalation Suspension for Treatment-Refractory Lung Disease Caused by Mycobacterium avium Complex (CONVERT). A Prospective, Open-Label, Randomized Study.
Griffith, David E; Eagle, Gina; Thomson, Rachel; Aksamit, Timothy R; Hasegawa, Naoki; Morimoto, Kozo; Addrizzo-Harris, Doreen J; O'Donnell, Anne E; Marras, Theodore K; Flume, Patrick A; Loebinger, Michael R; Morgan, Lucy; Codecasa, Luigi R; Hill, Adam T; Ruoss, Stephen J; Yim, Jae-Joon; Ringshausen, Felix C; Field, Stephen K; Philley, Julie V; Wallace, Richard J; van Ingen, Jakko; Coulter, Chris; Nezamis, James; Winthrop, Kevin L.
Afiliación
  • Griffith DE; 1 The University of Texas Health Science Center at Tyler, Tyler, Texas.
  • Eagle G; 2 Insmed Incorporated, Bridgewater, New Jersey.
  • Thomson R; 3 University of Queensland, Gallipoli Medical Research Institute, Brisbane, Queensland, Australia.
  • Aksamit TR; 4 Pulmonary Disease and Critical Care Medicine, Mayo Clinic, Rochester, Minnesota.
  • Hasegawa N; 5 Keio University Hospital, Tokyo, Japan.
  • Morimoto K; 6 Fukujuji Hospital, Japan Anti-Tuberculosis Association, Tokyo, Japan.
  • Addrizzo-Harris DJ; 7 Division of Pulmonary, Critical Care and Sleep Medicine, New York University School of Medicine, New York, New York.
  • O'Donnell AE; 8 Division of Pulmonary, Critical Care and Sleep Medicine, Georgetown University Hospital, Washington, District of Columbia.
  • Marras TK; 9 Department of Medicine, University of Toronto, and Toronto Western Hospital, University Health Network, Toronto, Ontario, Canada.
  • Flume PA; 10 Medical University of South Carolina, Charleston, South Carolina.
  • Loebinger MR; 11 Host Defense Unit, Royal Brompton Hospital, and Imperial College, London, United Kingdom.
  • Morgan L; 12 Concord Clinical School, University of Sydney, Sydney, New South Wales, Australia.
  • Codecasa LR; 13 TB Reference Centre, Villa Marelli Institute/Niguarda Hospital, Milan, Italy.
  • Hill AT; 14 Department of Respiratory Medicine, Royal Infirmary of Edinburgh and Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
  • Ruoss SJ; 15 Division of Pulmonary and Critical Care Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California.
  • Yim JJ; 16 Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University College of Medicine, Seoul, South Korea.
  • Ringshausen FC; 17 Department of Respiratory Medicine, Hannover Medical School, and German Center for Lung Research, Hannover, Germany.
  • Field SK; 18 Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Philley JV; 1 The University of Texas Health Science Center at Tyler, Tyler, Texas.
  • Wallace RJ; 1 The University of Texas Health Science Center at Tyler, Tyler, Texas.
  • van Ingen J; 19 Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Coulter C; 20 Queensland Mycobacterium Reference Laboratory, Pathology Queensland, Brisbane, Australia; and.
  • Nezamis J; 2 Insmed Incorporated, Bridgewater, New Jersey.
  • Winthrop KL; 21 OHSU-PSU School of Public Health, Portland, Oregon.
Am J Respir Crit Care Med ; 198(12): 1559-1569, 2018 12 15.
Article en En | MEDLINE | ID: mdl-30216086
ABSTRACT
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 (21) 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).
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Amicacina / Infección por Mycobacterium avium-intracellulare / Enfermedades Pulmonares / Antibacterianos Tipo de estudio: Clinical_trials / Guideline / Observational_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Amicacina / Infección por Mycobacterium avium-intracellulare / Enfermedades Pulmonares / Antibacterianos Tipo de estudio: Clinical_trials / Guideline / Observational_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2018 Tipo del documento: Article