Effects of omalizumab in Aspergillus-associated airway disease.

نویسندگان

  • L A Pérez-de-Llano
  • M C Vennera
  • A Parra
  • J Guallar
  • M Marin
  • O Asensio
  • P Ausin
  • L Borderías
  • C Fernández
  • C Granel
  • A Pérez-Pimiento
  • M Rubio
چکیده

The clinical spectrum of Aspergillus-associated airway diseases (AAAD) includes Aspergillus-induced asthma, allergic bron-chopulmonary aspergillosis (ABPA) and bronchocentric granulomatosis. Corticoste-roids are almost always used to suppress the immunological response to the fungal anti-gens. 1 Although there are no evidence-based alternative treatment options besides steroids, the well-known adverse effects of these drugs have prompted clinicians to look beyond this standard practice and several cases of ABPA patients with very positive outcomes after omalizumab therapy have been recently published. 2e6 We recruited 18 patients (13 women; mean age 49617 years) with AAAD (2 of them had been previously diagnosed with cystic fibrosis) from 11 Spanish hospitals. All of them had been treated with omali-zumab for at least 16 weeks and they were receiving inhaled corticosteroids (daily dose 13516554 mg budesonide or its equivalent) and a long-acting b2 agonist at the moment of omalizumab initiation. Seventeen patients were being treated with oral corticosteroids at a median daily dose of 16 mg prednisone or its equivalent (IQR 6e28) and 10 with itraconazole. The mean number of albuterol puffs per day was 3.5 (range 1e8). Prior to omalizumab administration, IgE levels were (median (IQR)) 698 IU/ml (478e977) and the median absolute count of eosinophils in blood was 610 mm 3 (317e1015). Sixteen of the 18 patients had CT-diagnosed bronchi-ectasis and fleeting pulmonary opacities were identified in 10 of them. All patients showed a delayed positive skin test for Aspergillus and 17 also developed an immediate response. Serum Aspergillus-specific IgE was found in all patients and precipitating antibodies in serum were observed in 10. Omalizumab-treated patients were followed up for a median of 36 weeks (IQR, 28e42). The mean dose of omalizumab per week was 6086108 mg. No significant adverse effects were observed. The treatment was discontinued in five patients due to a lack of response and in another patient because of a positive test for pregnancy. The clinical and functional effects of omalizumab are summarised in table 1. In this series, the largest reported to date, omalizumab has demonstrated a beneficial effect in reducing symptoms and exacerba-tions in a group of patients with AAAD. It also seems to improve pulmonary function even when oral corticosteroids were reduced or discontinued. Given the retrospective nature of this study and the small number of cases analysed, the results must be interpreted with caution. Although all patients met the criteria of APBA proposed by Rosenberg, 7 the differentiation between this …

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عنوان ژورنال:
  • Thorax

دوره 66 6  شماره 

صفحات  -

تاریخ انتشار 2011