Biologics in T2 Severe Asthma: Unveiling Different Effectiveness by Real-World Indirect Comparison
<b>Background</b>: Indirect comparison among biologics in severe asthma (SA) is a challenging but desirable goal for clinicians in real life. The aim of the study is to define characteristics of a biologic-treated T2-driven-SA population and to evaluate the effectiveness of biologic treatments in a real-world setting by variation in intra/inter-biologic parameters in an up to 4-year follow-up. <b>Methods</b>: Demographic, clinical, functional, and biological characteristics were evaluated retrospectively in 104 patients recruited until July 2022 at baseline (T0) and over a maximum of 4 years (T4) of biologic therapy (omalizumab/OmaG = 41, from T0 to T4, mepolizumab/MepoG = 26, from T0 to T4, benralizumab/BenraG = 18, from T0 to T2, and dupilumab/DupiG = 19, from T0 to T1). Variations of parameters using means of paired Delta were assessed. <b>Results</b>: At baseline, patients had high prevalence of T2-driven comorbidities, low asthma control test (ACT mean 17.65 ± 4.41), impaired pulmonary function (FEV<sub>1</sub> 65 ± 18 %pred), frequent exacerbations/year (AEs 3.5 ± 3), and OCS dependence (60%). DupiG had lower T2 biomarkers/comorbidities and AEs, and worse FEV<sub>1</sub> (57 ± 19 %pred) compared to other biologics (<i>p</i> < 0.05). All biologics improved ACT, FEV<sub>1</sub>%, FVC%, AEs rate, and OCS use. FEV<sub>1</sub>% improved in MepoG and BenraG over the minimal clinically important difference and was sustained over 4 years in OmaG and MepoG. A significant RV reduction in OmaG (T4) and DupiG (T1), and BenraG normalization (T2) of airflow limitation were found. We observed through inter-biologic parameters pair delta variation comparison a significant nocturnal awakenings reduction in BenraG vs. OmaG/MepoG, and neutrophils reduction in BenraG/DupiG vs. OmaG. <b>Conclusions</b>: Indirect comparison among biologics unveils clinical and functional improvements that may mark a different effectiveness. These results may highlight the preference of a single biologic compared to another with regard to specific treatable traits.
Authors
- Mattia Brusamento
- Vitina Carriero (ORCID: https://orcid.org/0000-0003-1866-5206)
- Elisa Arrigo (ORCID: https://orcid.org/0000-0003-1976-7466)
- Stefano Pizzimenti (ORCID: https://orcid.org/0000-0001-7723-8859)
- Sonia Garino
- Fabio Luigi Massimo Ricciardolo (ORCID: https://orcid.org/0000-0003-1826-5018)
- Giuseppe Guida (ORCID: https://orcid.org/0000-0003-3876-8587)
- Stefano Levra (ORCID: https://orcid.org/0000-0002-5745-7701)
- Fabiana Giannoccaro
- Francesca Bertolini (ORCID: https://orcid.org/0000-0003-4390-0394)
- Elisa Riccardi
- Erica Falzone
Institutions
- Istituto di Farmacologia Traslazionale (IT)
- National Research Council (IT)
- Ospedale San Luigi Gonzaga (IT)
- University of Turin (IT)
Publication Details
- Journal
- Journal of Clinical Medicine
- Published
- 2024-08-13
- DOI
- https://doi.org/10.3390/jcm13164750
- Citations
- 1
- Primary Topic
- Asthma and respiratory diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.33
Funders
- AstraZeneca
- Sanofi