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Amikacin Liposome Inhalation Suspension in the Real-World Management of Refractory Mycobacterium avium Complex
Toyoshi Yanagihara1, Hiroaki Ogata1, Asami Mori2
1Respiratory Medicine, National Hospital Organization Fukuoka National Hospital, Fukuoka, JPN.
Abstract:
The increasing prevalence of Mycobacterium avium complex (MAC) pulmonary disease poses a significant therapeutic challenge, particularly due to the limited efficacy and systemic toxicity associated with conventional guideline-based therapy. Amikacin liposome inhalation suspension (ALIS) has been developed, yet its real-world application remains underreported. This retrospective analysis, conducted from March 2021 to February 2024, examined ALIS's clinical use in patients aged 20 years or older with refractory MAC pulmonary disease at our institution. The primary objective of this study is to describe the patient characteristics and clinical trajectories associated with the initiation of ALIS therapy in real-world settings for individuals diagnosed with MAC pulmonary disease. Of 11 patients initiated on ALIS, one was excluded due to financial constraints impacting continuation. The analysis proceeded with the remaining 10 subjects. The mean age of participants was 70.2 years, with a predominance of female patients (n = 7, 70%) and a higher incidence of M. avium infections (n = 6, 60%). Forty percent of the cohort (n = 4) had a history of ethambutol-induced optic neuritis leading to the cessation of the drug. The average interval from the initiation of guideline-based therapy to the start of ALIS was 8.5 ± 6.9 years (mean ± standard deviation). The majority (80%) presented with positive Gaffky scores at ALIS initiation, and a significant proportion exhibited resistance to clarithromycin and ethambutol. Comorbid conditions, including diabetes and previous cancer, were noted. The study also observed elevated anti-MAC antibody levels. Treatment duration varied, with fatigue leading to discontinuation in two cases. Treatment-emergent adverse events were documented in individual patients, each presenting with grade 1 severity: hemoptysis (n = 1, 10%), elevated creatinine levels (n = 1, 10%), and dysphonia (n = 2, 20%) were observed, respectively. Correlation analysis revealed a significant inverse relationship between body mass index (BMI) and ALIS discontinuation due to fatigue, and a positive correlation between Gaffky scores and C-reactive protein (CRP) levels. These results underscore the potential benefits and limitations of ALIS, suggesting that timely intervention and comprehensive healthcare support are crucial for optimal outcomes in the treatment of advanced MAC pulmonary disease.
Insights
Amikacin liposome inhalation suspension (ALIS) shows real-world potential for refractory Mycobacterium avium complex (MAC) lung disease, despite some treatment discontinuations due to fatigue and mild adverse events. Further research is needed to optimize its use.
Area of Science:
- Pulmonology
- Infectious Diseases
- Pharmacology
Background:
- Mycobacterium avium complex (MAC) pulmonary disease presents treatment challenges due to limited efficacy and toxicity of standard therapies.
- Amikacin liposome inhalation suspension (ALIS) offers a novel therapeutic option, but real-world data on its application are scarce.
Purpose of the Study:
- To describe patient characteristics and clinical outcomes of ALIS initiation in a real-world setting for refractory MAC pulmonary disease.
- To evaluate the safety and tolerability of ALIS in this patient population.
Main Methods:
- Retrospective analysis of 10 adult patients with refractory MAC pulmonary disease initiated on ALIS between March 2021 and February 2024.
- Data collection included patient demographics, infection details, treatment history, adverse events, and treatment discontinuation reasons.
Main Results:
- The cohort (mean age 70.2 years) predominantly comprised females with M. avium infections, often with prior treatment failures and drug resistance.
- Commonly observed treatment-emergent adverse events were mild (Grade 1), including dysphonia, hemoptysis, and elevated creatinine.
- Fatigue led to ALIS discontinuation in two patients, inversely correlated with body mass index (BMI).
Conclusions:
- ALIS demonstrates potential in managing refractory MAC pulmonary disease in real-world clinical practice.
- Timely intervention and supportive care are vital for optimizing ALIS treatment outcomes.
- Further investigation is warranted to fully understand ALIS's long-term efficacy and safety profile.
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