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Can the response to Omalizumab be influenced by treatment duration? A real-life study.

Authors :
Sposato B
Scalese M
Latorre M
Novelli F
Scichilone N
Milanese M
Olivieri C
Perrella A
Paggiaro P
Source :
Pulmonary pharmacology & therapeutics [Pulm Pharmacol Ther] 2017 Jun; Vol. 44, pp. 38-45. Date of Electronic Publication: 2017 Mar 14.
Publication Year :
2017

Abstract

Objective: It is unknown whether Omalizumab effectiveness changes over the course of time. Our retrospective real-life study tried to analyze whether Omalizumab response may be influenced by treatment duration.<br />Methods: 340 severe asthmatics treated with Omalizumab for different periods of time were recruited. They were subdivided into 4 groups according to the Omalizumab treatment length: <12, between 12 and 24, between 24 and 60 and >60 months. Omalizumab treatment results (FEV <subscript>1</subscript> , exacerbations, ACT, SABA use, asthma control levels, medications used e and ICS doses) were compared.<br />Results: ACT, exacerbations, GINA control levels, ICS doses and SABA use were similar in all groups with different Omalizumab treatment durations. Using a linear regression model, corrected for all confounding variables, a higher significant positive increase in FEV <subscript>1</subscript> % in subjects treated for 12-24 (β = 9.49; p = 0.034) or 24-60 months (β = 8.56; p = 0.043) was found when compared with subjects treated for a shorter period. Treatment duration was positively associated with a step down of the other associated therapies (OR: 1.013; p = 0.019). This association was more relevant (OR: 4.167; p = 0.005) when we considered Omalizumab treatment duration >60 months compared to the shorter therapy. In particular, the percentage of subjects that were taking Montelukast, LABAs and oral corticosteroids was lower in the group treated with Omalizumab for a longer period of time.<br />Conclusion: In real-life, the positive Omalizumab response remained stable for over 60 months. Long term Omalizumab treatment may lead to a discontinuation of some associated medications and to a slowing down of FEV <subscript>1</subscript> decline.<br /> (Copyright © 2017 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1522-9629
Volume :
44
Database :
MEDLINE
Journal :
Pulmonary pharmacology & therapeutics
Publication Type :
Academic Journal
Accession number :
28302544
Full Text :
https://doi.org/10.1016/j.pupt.2017.03.004