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Impact of omalizumab on treatment of severe allergic asthma in UK clinical practice: a UK multicentre observational study (the APEX II study)
  1. Robert M Niven1,
  2. Dinesh Saralaya2,
  3. Rekha Chaudhuri3,
  4. Matthew Masoli4,
  5. Ian Clifton5,
  6. Adel H Mansur6,
  7. Victoria Hacking7,
  8. Susan McLain-Smith8,
  9. Andrew Menzies-Gow9
  1. 1Manchester Academic Health Science Centre, The University of Manchester & University Hospital of South Manchester, Manchester, UK
  2. 2Department of Respiratory Medicine, Bradford Teaching Hospitals NHS Foundation Trust, Bradford, UK
  3. 3Department of Respiratory Medicine, Gartnavel General Hospital, Glasgow, UK
  4. 4Department of Respiratory Medicine, Plymouth Hospitals NHS Trust, Plymouth, UK
  5. 5Department of Respiratory Medicine, St James's University Hospital, Leeds, UK
  6. 6Birmingham Regional Severe Asthma Service, Birmingham Heartlands Hospital, Birmingham, UK
  7. 7Novartis Pharmaceuticals UK Ltd, Frimley, UK
  8. 8pH Associates, Marlow, UK
  9. 9Department of Asthma and Allergy, Royal Brompton Hospital, London, UK
  1. Correspondence to Dr Robert M Niven; Robert.Niven{at}UHSM.NHS.UK

Abstract

Objective To describe the impact of omalizumab on asthma management in patients treated as part of normal clinical practice in the UK National Health Service (NHS).

Design A non-interventional, mixed methodology study, combining retrospective and prospective data collection for 12 months pre-omalizumab and post-omalizumab initiation, respectively.

Setting Data were collected in 22 UK NHS centres, including specialist centres and district general hospitals in the UK.

Participants 258 adult patients (aged ≥16 years; 65% women) with severe persistent allergic asthma treated with omalizumab were recruited, of whom 218 (84.5%) completed the study.

Primary and secondary outcome measures The primary outcome measure was change in mean daily dose of oral corticosteroids (OCS) between the 12-month pre-omalizumab and post-omalizumab initiation periods. A priori secondary outcome measures included response to treatment, changes in OCS dosing, asthma exacerbations, lung function, employment/education, patient-reported outcomes and hospital resource utilisation.

Results The response rate to omalizumab at 16 weeks was 82.4%. Comparing pre-omalizumab and post-omalizumab periods, the mean (95% CIs) daily dose of OCS decreased by 1.61 (−2.41 to −0.80) mg/patient/day (p<0.001) and hospital exacerbations decreased by 0.97 (−1.19 to −0.75) exacerbations/patient (p<0.001). Compared with baseline, lung function, assessed by percentage of forced expiratory volume in 1 s, improved by 4.5 (2.7 to 6.3)% at 16 weeks (p<0.001; maintained at 12 months) and patient quality of life (Asthma Quality of Life Questionnaire) improved by 1.38 (1.18 to 1.58) points at 16 weeks (p<0.001, maintained at 12 months). 21/162 patients with complete employment data gained employment and 6 patients lost employment in the 12-month post-omalizumab period. The mean number of A&E visits, inpatient hospitalisations, outpatient visits (excluding for omalizumab) and number of bed days/patient decreased significantly (p<0.001) in the 12-month post-omalizumab period.

Conclusions These data support the beneficial effects of omalizumab on asthma-related outcomes, quality of life and resource utilisation in unselected patients treated in ‘real-world’ clinical practice.

  • Severe asthma
  • omalizumab
  • corticosteroids
  • exacerbations

This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/

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