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Rate and predictors of biologic initiation in patients with severe asthma: a retrospective cohort study
John J Oppenheimer1, Tom Corbridge2, Alexandra Stach-Klysh2
1Pulmonary and Allergy Associates, Department of Internal Medicine, Rutgers New Jersey Medical School, 150 Bergen Street, Newark, NJ 07103, USA.
Background:
Biologic therapy uptake for poorly controlled severe asthma is suboptimal despite guideline recommendations.
Objectives:
To evaluate real-world biologic initiation trends and predictors among patients with severe uncontrolled asthma (SUA) and SUA with eosinophilic phenotype (SUA-EP).
Design:
A retrospective real-world cohort study that used Komodo Health administrative claims to identify US patients with SUA (controller/rescue medication use and ⩾2 asthma exacerbations in a year) and a subgroup of patients with SUA-EP (blood eosinophil count ⩾150 cells/µL in the year pre- or post-exacerbation).
Methods:
Biologic initiation trends following first asthma exacerbation were assessed, and factors associated with lack of biologic initiation following second exacerbation (SUA-EP only) were identified using LASSO regression models; odds ratios (OR), 95% confidence intervals (CIs), and p-values were calculated using logistic regression.
Results:
Biologic initiation rates following the first exacerbation were low at 12.7% (4360/34,246) and 12.2% (309/2526) of patients with SUA and SUA-EP, respectively; mean time between second exacerbation and initiation was 13.4 and 11.9 months. Predictors of lack of biologic initiation included young age (12-17 years; OR (95% CI) 3.65 (1.69-7.89)), primary care physician specialty at index relative to respiratory specialist (2.89 (2.04-4.10)), and antibiotic use (2.29 (1.44-3.66); all p < 0.05), indicating that younger patients, those managed by primary care and those treated with antibiotics for exacerbations, were less likely to receive biologics. Biologic initiation was more likely among patients with a cumulative systemic corticosteroid dose ⩾500 mg (prednisone equivalent; 0.38 (0.25-0.57)), those using leukotriene modifiers (0.42 (0.28-0.62)) or single-inhaler triple therapy (0.06 (0.01-0.40)), and those with eosinophilic disorders (0.19 (0.07-0.52); all p < 0.05).
Conclusion:
Despite eligibility, most patients with SUA and SUA-EP did not receive any biologic; younger age and primary care management were predictors of lack of biologic initiation. This highlights the need for improved specialist referral and biologic uptake.
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