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. 2024 Mar 27;17:273–290. doi: 10.2147/JAA.S438981

Table 3.

Proportion of Patients Achieving OCS Dose Reduction and/or Interruption During Benralizumab Treatment in Naïve, Bio-Experienced, Omalizumab, and Mepolizumab Groups After 48 and 96 Weeks

OCS Reduction from Index Date Naive at 48 Weeks N (%) (N=25) Naive at 96 Weeks N (%) (N=22) Bio-Experienced at 48 Weeks N (%) (N=9) Bio-Experienced at 96 Weeks N (%) (N=8) Omalizumab at 48 Weeks N (%) (N=3) Omalizumab at 96 Weeks N (%) (N=3) Mepolizumab at 48 Weeks N (%) (N=6) Mepolizumab at 96 Weeks N (%) (N=5)
Interruption 13 (52.0) 14 (63.6) 5 (55.6) 4 (50.0) 1 (33.3) 1 (33.3) 4 (66.7) 3 (60.0)
Any reduction (including interruption) 15 (60.0) 15 (68.2) 6 (66.7) 5 (62.5) 2 (66.7) 2 (66.7) 4 (66.7) 3 (60.0)
≥90% dose reduction 13 (52.0) 14 (63.6) 5 (55.6) 4 (50.0) 1 (33.3) 1 (33.3) 4 (66.7) 3 (60.0)
≥75% dose reduction 13 (52.0) 14 (63.6) 5 (55.6) 4 (50.0) 1 (33.3) 1 (33.3) 4 (66.7) 3 (60.0)
≥25% dose reduction 15 (60.0) 15 (68.2) 5 (55.6) 4 (50.0) 1 (33.3) 1 (33.3) 4 (66.7) 3 (60.0)
No reduction 10 (40.0) 7 (31.8) 3 (33.3) 3 (37.5) 1 (33.3) 1 (33.3) 2 (33.3) 2 (40.0)

Notes: OCS dosage is expressed as daily mg (prednisone equivalent). Data are expressed as N (%).

Abbreviations: N, number of patients; OCS, oral corticosteroids.