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Clinical Efficacy of Benralizumab in Patients With Severe, Uncontrolled Eosinophilic Asthma and Nasal Polyposis: Pooled Analysis of the SIROCCO and CALIMA Trials
Saturday, March 3, 2018
South Hall A2 (Convention Center)
Jorge Maspero, Tim Harrison, Viktoria Werkström, Yanping Wu, Gokul Gopalan, James Zangrilli
RATIONALE: Nasal polyposis (NP) has been associated with an eosinophilic asthma phenotype and may predict benralizumab’s efficacy.

METHODS: Post-hoc pooled analysis of the Phase III SIROCCO (48 weeks; Lancet. 2016;388:2115–27) and CALIMA (56 weeks; Lancet. 2016;388:2128–41) trials. Patients aged ≥12 years receiving high-dosage ICS/LABA with baseline blood eosinophils ≥300 cells/µL received benralizumab 30 mg SC every 8 weeks (Q8W; n=506) or placebo (n=515).

RESULTS: Patients with NP (NP+) generally had greater mean blood eosinophil counts (Q8W: 668 cells/µL; placebo: 749 cells/µL) than patients without NP (NP; Q8W: 606 cells/µL; placebo: 597 cells/µL). Baseline maintenance OCS use was also greater for NP+ (Q8W: 31.3%; placebo: 21.4%) than NP (Q8W: 10.5%; placebo: 10.1%). Placebo exacerbation rates during treatment were 1.27 (n=515), 1.74 (n=117), and 1.13 (n=398) for the overall, NP+, and NPgroups, respectively. Compared with placebo, benralizumab Q8W reduced exacerbation rates by 42% for all patients (rate ratio [RR], 0.58 [95% CI, 0.48–0.70], p<0.001; n=506), by 54% for NP+ (RR, 0.46 [95% CI, 0.31–0.69], p<0.001; n=115), and by 38% for NP (RR, 0.62 [95% CI, 0.50–0.78], p<0.001; n=391); and increased prebronchodilator FEV1 by 0.128 L for all patients (95% CI, 0.064–0.191, p<0.001; n=502), by 0.272 L for NP+ (95% CI, 0.124–0.421, p<0.001; n=115), and by 0.102 L for NP(95% CI, 0.032–0.172, p=0.004; n=387). Similar trends were observed for efficacy measures of asthma symptoms (ACQ-6) and asthma-related quality of life (AQLQ[S]+12).

CONCLUSIONS: Benralizumab demonstrated enhanced clinical efficacy for patients with severe, uncontrolled eosinophilic asthma and NP.