TY - JOUR
T1 - A Phase II, Multicenter, Randomized, Placebo-Controlled Study of Benralizumab, a Humanized Anti-IL-5R Alpha Monoclonal Antibody, in Patients With Eosinophilic Chronic Rhinosinusitis
AU - Takabayashi, Tetsuji
AU - Asaka, Daiya
AU - Okamoto, Yoshitaka
AU - Himi, Tetsuo
AU - Haruna, Shinichi
AU - Yoshida, Naohiro
AU - Kondo, Kenji
AU - Yoshikawa, Mamoru
AU - Sakuma, Yasunori
AU - Shibata, Kunihiko
AU - Suzuki, Motohiko
AU - Kobayashi, Masayoshi
AU - Kawata, Ryo
AU - Tsuzuki, Kenzo
AU - Okano, Mitsuhiro
AU - Higaki, Takaya
AU - Takeno, Sachio
AU - Kodama, Satoru
AU - Yonekura, Syuji
AU - Saito, Hiromi
AU - Nozaki, Akiyo
AU - Otori, Nobuyoshi
AU - Fujieda, Shigeharu
N1 - Funding Information:
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by Kyowa Kirin Co., Ltd.
Funding Information:
We would like to thank the patients, investigators, and site staff who participated in this study. We would also like to thank AstraZeneca for their specific advice on the study. Editing assistance was provided by Serina Stretton, PhD, CMPP, and Jacqueline Atkinson, BA (Hons), of Envision Pharma Group and was funded by Kyowa Kirin Co., Ltd.
Publisher Copyright:
© The Author(s) 2021.
PY - 2021/11
Y1 - 2021/11
N2 - Background: Strong eosinophil infiltration in chronic rhinosinusitis with nasal polyp (CRSwNP) is highly associated with recalcitrance and higher nasal polyp recurrence rate after surgery. The prevalence of eosinophilic CRSwNP (ECRS) is increasing in Asian countries including Japan. Benralizumab is a humanized anti-IL-5R alpha monoclonal antibody that depletes eosinophils by antibody-dependent cell-mediated cytotoxicity. Objective: To assess the efficacy and safety of benralizumab in patients with ECRS. Methods: This phase II, randomized, double-blind, placebo-controlled study was conducted in Japan. Patients were randomized 1:2:2 to placebo, a single administration of benralizumab 30 mg, or benralizumab 30 mg every 4 weeks (q4w) for a total of three doses. The primary endpoint was the change in nasal polyp score from baseline at Week 12. Results: Overall, 56 patients were enrolled (placebo, n = 11; benralizumab single dose, n = 22; benralizumab q4w, n = 23). Although the mean total nasal polyp score began to decrease after the initiation of benralizumab treatment, there were no statistically significant differences in change in nasal polyp score from baseline at Week 12 between benralizumab and placebo (placebo, −0.5 ± 0.8; benralizumab single, −0.3 ± 0.8; benralizumab q4w, −0.5 ± 1.5). Post-hoc analysis showed that the administration of benralizumab decreased nasal polyp scores ≥2 points in 42.2% of ECRS patients and that patients with high blood eosinophil levels had a greater tendency to respond to benralizumab treatment. The safety profile was similar to that in previous studies and no unexpected adverse events were noted. Conclusion: Although benralizumab did not meet the primary efficacy endpoint, reductions of nasal polyp scores were seen in the benralizumab group compared with the placebo group over the whole study period, especially in patients with high levels of blood eosinophils.
AB - Background: Strong eosinophil infiltration in chronic rhinosinusitis with nasal polyp (CRSwNP) is highly associated with recalcitrance and higher nasal polyp recurrence rate after surgery. The prevalence of eosinophilic CRSwNP (ECRS) is increasing in Asian countries including Japan. Benralizumab is a humanized anti-IL-5R alpha monoclonal antibody that depletes eosinophils by antibody-dependent cell-mediated cytotoxicity. Objective: To assess the efficacy and safety of benralizumab in patients with ECRS. Methods: This phase II, randomized, double-blind, placebo-controlled study was conducted in Japan. Patients were randomized 1:2:2 to placebo, a single administration of benralizumab 30 mg, or benralizumab 30 mg every 4 weeks (q4w) for a total of three doses. The primary endpoint was the change in nasal polyp score from baseline at Week 12. Results: Overall, 56 patients were enrolled (placebo, n = 11; benralizumab single dose, n = 22; benralizumab q4w, n = 23). Although the mean total nasal polyp score began to decrease after the initiation of benralizumab treatment, there were no statistically significant differences in change in nasal polyp score from baseline at Week 12 between benralizumab and placebo (placebo, −0.5 ± 0.8; benralizumab single, −0.3 ± 0.8; benralizumab q4w, −0.5 ± 1.5). Post-hoc analysis showed that the administration of benralizumab decreased nasal polyp scores ≥2 points in 42.2% of ECRS patients and that patients with high blood eosinophil levels had a greater tendency to respond to benralizumab treatment. The safety profile was similar to that in previous studies and no unexpected adverse events were noted. Conclusion: Although benralizumab did not meet the primary efficacy endpoint, reductions of nasal polyp scores were seen in the benralizumab group compared with the placebo group over the whole study period, especially in patients with high levels of blood eosinophils.
KW - benralizumab
KW - chronic rhinosinusitis
KW - efficacy
KW - eosinophil
KW - eosinophilic chronic rhinosinusitis with nasal polyp
KW - interleukin-5
KW - nasal polyp
KW - phase II clinical trial
KW - randomized
KW - safety
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U2 - 10.1177/19458924211009429
DO - 10.1177/19458924211009429
M3 - Article
C2 - 33840229
AN - SCOPUS:85104319345
SN - 1945-8924
VL - 35
SP - 861
EP - 870
JO - American Journal of Rhinology and Allergy
JF - American Journal of Rhinology and Allergy
IS - 6
ER -