Observational study in severe asthmatic patients after discontinuation of omalizumab for good asthma control

Summary Introduction Severe persistent asthma represents a major and costly public health issue. There is evidence that long-term treatment with omalizumab might have disease-modifying activity but data on the consequences of discontinuing treatment after a positive response are limited. The purpose...

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Veröffentlicht in:Respiratory medicine 2014-04, Vol.108 (4), p.571-576
Hauptverfasser: Molimard, M, Mala, L, Bourdeix, I, Le Gros, V
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container_title Respiratory medicine
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creator Molimard, M
Mala, L
Bourdeix, I
Le Gros, V
description Summary Introduction Severe persistent asthma represents a major and costly public health issue. There is evidence that long-term treatment with omalizumab might have disease-modifying activity but data on the consequences of discontinuing treatment after a positive response are limited. The purpose of this study was to investigate—in real-life prescribing conditions—what happens when omalizumab is discontinued in patients with severe, persistent allergic asthma who have responded well to omalizumab treatment. Methods An observational, descriptive, cross-sectional, retrospective study to establish the time to loss of asthma control after the discontinuation of courses of omalizumab treatment of varying duration. Results 24 lung specialists reviewed data from 61 responder patients who had discontinued omalizumab after a mean duration of 22.7 ± 13.1 [range: 2.5; 59.5] months of treatment. Loss of asthma control was documented in 34 patients (55.7%) with a median interval between discontinuation and loss of control of 13.0 months (mean 20.4 ± 2.6 [95% CI: 8.3–28.1]). No correlation was detected between time to loss of control and duration of treatment, although control tended to be sustained for longer in patients whose response had been classified as “excellent” as opposed to “good” (median: 17.0 vs. 12.8 months; NS). Discussion The discontinuation of omalizumab was not associated with any rebound effect or exacerbation of the disease, and control was sustained throughout the follow-up period of at least 6 months in nearly half of all patients, including all of those who had been treated for 3.5 years or more. After the reintroduction of omalizumab, 4 out of 20 patients did not respond again.
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There is evidence that long-term treatment with omalizumab might have disease-modifying activity but data on the consequences of discontinuing treatment after a positive response are limited. The purpose of this study was to investigate—in real-life prescribing conditions—what happens when omalizumab is discontinued in patients with severe, persistent allergic asthma who have responded well to omalizumab treatment. Methods An observational, descriptive, cross-sectional, retrospective study to establish the time to loss of asthma control after the discontinuation of courses of omalizumab treatment of varying duration. Results 24 lung specialists reviewed data from 61 responder patients who had discontinued omalizumab after a mean duration of 22.7 ± 13.1 [range: 2.5; 59.5] months of treatment. Loss of asthma control was documented in 34 patients (55.7%) with a median interval between discontinuation and loss of control of 13.0 months (mean 20.4 ± 2.6 [95% CI: 8.3–28.1]). No correlation was detected between time to loss of control and duration of treatment, although control tended to be sustained for longer in patients whose response had been classified as “excellent” as opposed to “good” (median: 17.0 vs. 12.8 months; NS). Discussion The discontinuation of omalizumab was not associated with any rebound effect or exacerbation of the disease, and control was sustained throughout the follow-up period of at least 6 months in nearly half of all patients, including all of those who had been treated for 3.5 years or more. After the reintroduction of omalizumab, 4 out of 20 patients did not respond again.</description><identifier>ISSN: 0954-6111</identifier><identifier>EISSN: 1532-3064</identifier><identifier>DOI: 10.1016/j.rmed.2014.02.003</identifier><identifier>PMID: 24565601</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Anti-Asthmatic Agents - administration &amp; dosage ; Anti-Asthmatic Agents - therapeutic use ; Antibodies, Anti-Idiotypic - administration &amp; dosage ; Antibodies, Anti-Idiotypic - therapeutic use ; Antibodies, Monoclonal, Humanized - administration &amp; dosage ; Antibodies, Monoclonal, Humanized - therapeutic use ; Asthma ; Asthma - drug therapy ; Asthma - physiopathology ; Asthma control ; Body mass index ; Child ; Confidence intervals ; Discontinuation ; Drug Administration Schedule ; Drug therapy ; Duration of treatment ; Female ; Forced Expiratory Volume - drug effects ; Humans ; Male ; Medical records ; Middle Aged ; Omalizumab ; Patients ; Physicians ; Population ; Pulmonary/Respiratory ; Recurrence ; Remission Induction ; Retrospective Studies ; Standard deviation ; Time Factors ; Treatment Outcome ; Withholding Treatment ; Young Adult</subject><ispartof>Respiratory medicine, 2014-04, Vol.108 (4), p.571-576</ispartof><rights>Elsevier Ltd</rights><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. 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There is evidence that long-term treatment with omalizumab might have disease-modifying activity but data on the consequences of discontinuing treatment after a positive response are limited. The purpose of this study was to investigate—in real-life prescribing conditions—what happens when omalizumab is discontinued in patients with severe, persistent allergic asthma who have responded well to omalizumab treatment. Methods An observational, descriptive, cross-sectional, retrospective study to establish the time to loss of asthma control after the discontinuation of courses of omalizumab treatment of varying duration. Results 24 lung specialists reviewed data from 61 responder patients who had discontinued omalizumab after a mean duration of 22.7 ± 13.1 [range: 2.5; 59.5] months of treatment. Loss of asthma control was documented in 34 patients (55.7%) with a median interval between discontinuation and loss of control of 13.0 months (mean 20.4 ± 2.6 [95% CI: 8.3–28.1]). No correlation was detected between time to loss of control and duration of treatment, although control tended to be sustained for longer in patients whose response had been classified as “excellent” as opposed to “good” (median: 17.0 vs. 12.8 months; NS). Discussion The discontinuation of omalizumab was not associated with any rebound effect or exacerbation of the disease, and control was sustained throughout the follow-up period of at least 6 months in nearly half of all patients, including all of those who had been treated for 3.5 years or more. 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There is evidence that long-term treatment with omalizumab might have disease-modifying activity but data on the consequences of discontinuing treatment after a positive response are limited. The purpose of this study was to investigate—in real-life prescribing conditions—what happens when omalizumab is discontinued in patients with severe, persistent allergic asthma who have responded well to omalizumab treatment. Methods An observational, descriptive, cross-sectional, retrospective study to establish the time to loss of asthma control after the discontinuation of courses of omalizumab treatment of varying duration. Results 24 lung specialists reviewed data from 61 responder patients who had discontinued omalizumab after a mean duration of 22.7 ± 13.1 [range: 2.5; 59.5] months of treatment. Loss of asthma control was documented in 34 patients (55.7%) with a median interval between discontinuation and loss of control of 13.0 months (mean 20.4 ± 2.6 [95% CI: 8.3–28.1]). No correlation was detected between time to loss of control and duration of treatment, although control tended to be sustained for longer in patients whose response had been classified as “excellent” as opposed to “good” (median: 17.0 vs. 12.8 months; NS). Discussion The discontinuation of omalizumab was not associated with any rebound effect or exacerbation of the disease, and control was sustained throughout the follow-up period of at least 6 months in nearly half of all patients, including all of those who had been treated for 3.5 years or more. After the reintroduction of omalizumab, 4 out of 20 patients did not respond again.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>24565601</pmid><doi>10.1016/j.rmed.2014.02.003</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Aged
Aged, 80 and over
Anti-Asthmatic Agents - administration & dosage
Anti-Asthmatic Agents - therapeutic use
Antibodies, Anti-Idiotypic - administration & dosage
Antibodies, Anti-Idiotypic - therapeutic use
Antibodies, Monoclonal, Humanized - administration & dosage
Antibodies, Monoclonal, Humanized - therapeutic use
Asthma
Asthma - drug therapy
Asthma - physiopathology
Asthma control
Body mass index
Child
Confidence intervals
Discontinuation
Drug Administration Schedule
Drug therapy
Duration of treatment
Female
Forced Expiratory Volume - drug effects
Humans
Male
Medical records
Middle Aged
Omalizumab
Patients
Physicians
Population
Pulmonary/Respiratory
Recurrence
Remission Induction
Retrospective Studies
Standard deviation
Time Factors
Treatment Outcome
Withholding Treatment
Young Adult
title Observational study in severe asthmatic patients after discontinuation of omalizumab for good asthma control
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