A Phase II, Multicenter, Randomized, Placebo-Controlled Study of Benralizumab, a Humanized Anti-IL-5R Alpha Monoclonal Antibody, in Patients With Eosinophilic Chronic Rhinosinusitis.

benralizumab chronic rhinosinusitis efficacy eosinophil eosinophilic chronic rhinosinusitis with nasal polyp interleukin-5 nasal polyp phase II clinical trial randomized safety

Journal

American journal of rhinology & allergy
ISSN: 1945-8932
Titre abrégé: Am J Rhinol Allergy
Pays: United States
ID NLM: 101490775

Informations de publication

Date de publication:
Nov 2021
Historique:
pubmed: 13 4 2021
medline: 3 11 2021
entrez: 12 4 2021
Statut: ppublish

Résumé

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. To assess the efficacy and safety of benralizumab in patients with ECRS. 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. 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. 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.

Sections du résumé

BACKGROUND 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 OBJECTIVE
To assess the efficacy and safety of benralizumab in patients with ECRS.
METHODS 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 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 CONCLUSIONS
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.

Identifiants

pubmed: 33840229
doi: 10.1177/19458924211009429
doi:

Substances chimiques

Anti-Asthmatic Agents 0
Antibodies, Monoclonal, Humanized 0
benralizumab 71492GE1FX

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

861-870

Auteurs

Tetsuji Takabayashi (T)

Department of Otorhinolaryngology-Head & Neck Surgery, University of Fukui, Fukui, Japan.

Daiya Asaka (D)

Department of Otorhinolaryngology, Jikei University School of Medicine, Tokyo, Japan.

Yoshitaka Okamoto (Y)

Department of Otorhinolaryngology, Head and Neck Surgery, Chiba University, Chiba, Japan.

Tetsuo Himi (T)

Department of Otolaryngology, Sapporo Medical University, Hokkaido, Japan.

Shinichi Haruna (S)

Department of Otorhinolaryngology, Head & Neck Surgery, Dokkyo Medical University, Tochigi, Japan.

Naohiro Yoshida (N)

Department of Otolaryngology, Jichi Medical University Saitama Medical Center, Saitama, Japan.

Kenji Kondo (K)

Department of Otolaryngology, University of Tokyo, Tokyo, Japan.

Mamoru Yoshikawa (M)

Department of Otorhinolaryngology, Toho University Ohashi Medical Center, Tokyo, Japan.

Yasunori Sakuma (Y)

Department of Otorhinolaryngology, Yokohama City University Medical Center, Kanagawa, Japan.
Kagami-Zaitaku Clinic, Kanagawa, Japan.

Kunihiko Shibata (K)

Department of Otorhinolaryngology, Yokohama City University Medical Center, Kanagawa, Japan.

Motohiko Suzuki (M)

Departments of Otorhinolaryngology, Nagoya City University, Aichi, Japan.

Masayoshi Kobayashi (M)

Department of Otorhinolaryngology-Head and Neck Surgery, Mie University Graduate School of Medicine, Mie, Japan.

Ryo Kawata (R)

Department of Otolaryngology, Head & Neck Surgery, Osaka Medical College, Osaka, Japan.

Kenzo Tsuzuki (K)

Department of Otolaryngology-Head and Neck Surgery, Hyogo College of Medicine, Hyogo, Japan.

Mitsuhiro Okano (M)

Department of Otorhinolaryngology, International University of Health and Welfare Mita Hospital, Tokyo, Japan.
Department of Otolaryngology-Head and Neck Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Takaya Higaki (T)

Department of Otolaryngology-Head and Neck Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Sachio Takeno (S)

Department of Otorhinolaryngology, Head and Neck Surgery, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.

Satoru Kodama (S)

Kodama Jibiinkoka Clinic, Oita, Japan.
Oita University Faculty of Medicine, Otolaryngology, Head and Neck Surgery, Oita, Japan.

Syuji Yonekura (S)

Department of Otorhinolaryngology, Head and Neck Surgery, Chiba University, Chiba, Japan.

Hiromi Saito (H)

R&D Division, Kyowa kirin Co., Ltd., Tokyo, Japan.

Akiyo Nozaki (A)

R&D Division, Kyowa kirin Co., Ltd., Tokyo, Japan.

Nobuyoshi Otori (N)

Department of Otorhinolaryngology, Jikei University School of Medicine, Tokyo, Japan.

Shigeharu Fujieda (S)

Department of Otorhinolaryngology-Head & Neck Surgery, University of Fukui, Fukui, Japan.

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