Treatable traits and personalised management of moderate-severe asthma: implications for reliever use, symptom control and exacerbation risk

<bold>Introduction:</bold> Patient characteristics affect symptom control, reliever medication (Rmed) use and exacerbation risk in asthma, but the overall impact of these potentially treatable traits is poorly understood. <bold>Aim:</bold> To evaluate how regular treatment (with fluticasone propionate [FP] monotherapy, FP-salmeterol [FP/SAL], or budesonide-formoterol [BUD/FOR]) affects personalised management of moderate-severe asthma. <bold>Methods:</bold> Simulation scenarios used models previously developed from pooled clinical trial data. Individual Rmed use patterns, symptom control levels (ACQ-5) and time to first exacerbation were predicted over 1 year. Switching patients with poor control from FP to FP/SAL or BUD/FOR was assessed, and treatment differences were tested for each endpoint. <bold>Results:</bold> Stepping up FP to FP/SAL or BUD/FOR led to significant reductions in Rmed use. Improvement in symptoms and decrease in Rmed use was less in patients with asthma history >10 years, higher baseline ACQ-5, obesity and in smokers. These patients had greater reductions in Rmed use and lower exacerbation risks with FP/SAL relative to BUD/FOR (p<0.01 for all comparisons; Figure 1). <bold>Conclusions:</bold> Treatment choice and patient baseline characteristics contribute to significant differences in immediate and long-term response. These findings support personalised management. <bold>Funding:</bold> GSK (ID 215310). <fig><object-id>erj;64/suppl_68/PA1181/F1</object-id><object-id>F1</object-id><object-id>F1</object-id><graphic></graphic></fig>

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Published
2024-09-14
DOI
https://doi.org/10.1183/13993003.congress-2024.pa1181
Primary Topic
Asthma and respiratory diseases
Type
article
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article

Treatable traits and personalised management of moderate-severe asthma: implications for reliever use, symptom control and exacerbation risk

Sourabh Fulmali, Sven C. van Dijkman, Anurita Majumdar, Janna K. Duong et al.
Asthma and respiratory diseases
article

Treatable traits and personalised management of moderate-severe asthma: implications for reliever use, symptom control and exacerbation risk

Sourabh Fulmali, Sven C. van Dijkman, Anurita Majumdar, Janna K. Duong, Sean Oosterholt, Dave Singh, Ian Pavord, Oscar E. Della Pasqua, Gabriel García
article en

Abstract

<bold>Introduction:</bold> Patient characteristics affect symptom control, reliever medication (Rmed) use and exacerbation risk in asthma, but the overall impact of these potentially treatable traits is poorly understood. <bold>Aim:</bold> To evaluate how regular treatment (with fluticasone propionate [FP] monotherapy, FP-salmeterol [FP/SAL], or budesonide-formoterol [BUD/FOR]) affects personalised management of moderate-severe asthma. <bold>Methods:</bold> Simulation scenarios used models previously developed from pooled clinical trial data. Individual Rmed use patterns, symptom control levels (ACQ-5) and time to first exacerbation were predicted over 1 year. Switching patients with poor control from FP to FP/SAL or BUD/FOR was assessed, and treatment differences were tested for each endpoint. <bold>Results:</bold> Stepping up FP to FP/SAL or BUD/FOR led to significant reductions in Rmed use. Improvement in symptoms and decrease in Rmed use was less in patients with asthma history >10 years, higher baseline ACQ-5, obesity and in smokers. These patients had greater reductions in Rmed use and lower exacerbation risks with FP/SAL relative to BUD/FOR (p<0.01 for all comparisons; Figure 1). <bold>Conclusions:</bold> Treatment choice and patient baseline characteristics contribute to significant differences in immediate and long-term response. These findings support personalised management. <bold>Funding:</bold> GSK (ID 215310). <fig><object-id>erj;64/suppl_68/PA1181/F1</object-id><object-id>F1</object-id><object-id>F1</object-id><graphic></graphic></fig>

Nuffield Orthopaedic Centre (GB), University of Oxford (GB), Manchester University NHS Foundation Trust (GB), GlaxoSmithKline (India) (IN), Biochemistry Research Institute of La Plata (AR), System Simulation (United Kingdom) (GB)
Openalex Percentile: Top 72%
Asthma and respiratory diseases
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