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Impact of body mass index on omalizumab response in adults with moderate-to-severe allergic asthma.
Geng, Bob; Dixon, Anne E; Ko, Jinnie; Janampally, Pranathi; Haselkorn, Tmirah; Holweg, Cecile T J; Casale, Thomas B; Jarjour, Nizar.
Afiliação
  • Geng B; The University of California San Diego School of Medicine, San Diego, California.
  • Dixon AE; University of Vermont Medical Center, Burlington, Vermont.
  • Ko J; Genentech, Inc., South San Francisco, California.
  • Janampally P; Genentech, Inc., South San Francisco, California.
  • Haselkorn T; Astellas Gene Therapies, San Francisco, California.
  • Holweg CTJ; Genentech, Inc., South San Francisco, California. Electronic address: holweg.cecile@gene.com.
  • Casale TB; Division of Allergy and Immunolgy, University of South Florida, Tampa, Florida.
  • Jarjour N; Department of Medicine, University of Wisconsin, Madison, Wisconsin.
Ann Allergy Asthma Immunol ; 128(5): 553-560, 2022 05.
Article em En | MEDLINE | ID: mdl-35101644
ABSTRACT

BACKGROUND:

Effectiveness of asthma treatment, including biologics, may be different in patients with higher body mass index (BMI).

OBJECTIVE:

To evaluate response to omalizumab (dosed by serum immunoglobulin E level and weight) by BMI category.

METHODS:

Pooled data from 2 randomized, double-blind, placebo-controlled studies of adults with moderate-to-severe allergic asthma were analyzed by BMI category (<25 kg/m2 [normal or underweight], n = 397; 25 to <30 kg/m2 [overweight], n = 330; ≥ 30 kg/m2 [obese], n = 268). Placebo-adjusted exacerbation rate reductions were evaluated by Poisson regression modeling. Changes from baseline in forced expiratory volume in 1 second, beclomethasone dipropionate (BDP) dose, Total Asthma Symptom Score, and Asthma Quality of Life Questionnaire were evaluated by analysis of covariance.

RESULTS:

Greater placebo-adjusted exacerbation rate reductions (95% confidence interval) were observed with increasing BMI (normal or underweight, -37.4% [-69.0% to 26.8%]; overweight, -52.7% [-78.4% to 3.7%]; obese, -71.9% [-86.9% to -39.5%]). There were no differences in forced expiratory volume in 1 second improvement between BMI categories at week 16 (normal or underweight, 76.2 [5.3-147.1] mL; overweight, 98.1 [13.9-182.4] mL; obese, 69.1 [-18.9 to 157.2] mL). No differences in BDP dose reduction (µg) were noted between BMI categories (normal or underweight, 23.0 [15.7-30.3]; overweight, 22.5 [13.5-31.5]; obese, 16.6 [5.8-27.3]). Fewer patients in the higher BMI categories eliminated BDP use. There were trends for smaller improvements with higher BMI in Total Asthma Symptom Score (normal/underweight, -0.52 [-0.82 to -0.22]; overweight, -0.50 [-0.80 to -0.20]; obese, -0.39 [-0.77 to 0.00]) and Asthma Quality of Life Questionnaire (normal or underweight, 0.34 [0.16-0.52]; overweight, 0.34 [0.13-0.55]; obese, 0.15 [-0.08 to 0.39]).

CONCLUSION:

Omalizumab provides benefit to patients with moderate-to-severe allergic asthma, regardless of BMI. TRIAL REGISTRATION Studies 008/009 were conducted before clinical trial registration was required, and therefore clinical trial registration numbers are not available.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma / Antiasmáticos Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma / Antiasmáticos Idioma: En Ano de publicação: 2022 Tipo de documento: Article