Exploring Definitions and Predictors of Severe Asthma Clinical Remission after Biologic Treatment in Adults
Articolo
Data di Pubblicazione:
2024
Abstract:
Rationale: There is no consensus on criteria to include in an asthma remission definition in real life. Factors associated with achieving remission after biologic initiation remain poorly understood. Objectives: To quantify the proportion of adults with severe asthma achieving multidomain-defined remission after biologic initiation and identify prebiologic characteristics associated with achieving remission that may be used to predict it. Methods: This was a longitudinal cohort study using data from 23 countries from the International Severe Asthma Registry. Four asthma outcome domains were assessed in the 1 year before and after biologic initiation. A priori-defined remission cutoffs were: 0 exacerbations/yr, no long-term oral corticosteroid (LTOCS), partly/well-controlled asthma, and percent predicted FEV1 > 80%. Remission was defined using two (exacerbations + LTOCS), three (+control or +lung function), and four of these domains. The association between prebiologic characteristics and postbiologic remission was assessed by multivariable analysis. Measurements and Main Results: A total of 50.2%, 33.5%, 25.8%, and 20.3% of patients met criteria for two-, three- (+control), three- (+lung function), and four-domain remission, respectively. The odds of achieving four-domain remission decreased by 15% for every additional 10 years of asthma duration (odds ratio, 0.85; 95% confidence interval, 0.73-1.00). The odds of remission increased in those with fewer exacerbations per year, lower LTOCS daily dose, better control, and better lung function before biologic initiation. Conclusions: One in five patients achieved four-domain remission within 1 year of biologic initiation. Patients with less severe impairment and shorter asthma duration at initiation had a greater chance of achieving remission after biologic treatment, indicating that biologic treatment should not be delayed if remission is the goal.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
anti-IL4Rα; anti-IL5/5R; anti-IgE; exacerbation; lung function
Elenco autori:
Perez-de-Llano, Luis; Scelo, Ghislaine; Tran, Trung N.; Le, Tham T.; Fagerås, Malin; Cosio, Borja G.; Peters, Matthew; Pfeffer, Paul E.; Al-Ahmad, Mona; Al-Lehebi, Riyad O.; Altraja, Alan; Bergeron, Celine; Bjermer, Leif H.; Bjerrum, Anne S.; Bulathsinhala, Lakmini; Busby, John; Cano Rosales, Diana J.; Canonica, Giorgio W.; Carter, Victoria A.; Charriot, Jeremy; Christoff, George C.; Denton, Eve J.; Dorscheid, Delbert R.; Fernandez Sanchez, Maria J.; Fonseca, João A.; Gibson, Peter G.; Goh, Celine Y. Y.; Heaney, Liam G.; Heffler, Enrico; Hew, Mark; Iwanaga, Takashi; Katial, Rohit; Koh, Mariko S.; Kuna, Piotr; Larenas-Linnemann, Désirée E. S.; Lehtimäki, Lauri; Mahboub, Bassam; Martin, Neil; Matsumoto, Hisako; Menzies-Gow, Andrew N.; Papadopoulos, Nikolaos G.; Popov, Todor A.; Porsbjerg, Celeste M.; Patel, Pujan; Rhee, Chin K.; Sadatsafavi, Mohsen; Taillé, Camille; Torres-Duque, Carlos A.; Tsai, Ming-Ju; Ulrik, Charlotte S.; Upham, John W.; von Bülow, Anna; Wang, Eileen; Wechsler, Michael E.; Price, David B.
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