Long-term "real-life" safety of omalizumab in patients with severe uncontrolled asthma: A nine-year study. (September 2017)
- Record Type:
- Journal Article
- Title:
- Long-term "real-life" safety of omalizumab in patients with severe uncontrolled asthma: A nine-year study. (September 2017)
- Main Title:
- Long-term "real-life" safety of omalizumab in patients with severe uncontrolled asthma: A nine-year study
- Authors:
- Di Bona, Danilo
Fiorino, Irene
Taurino, Marialuisa
Frisenda, Flavia
Minenna, Elena
Pasculli, Carlo
Kourtis, Georgios
Rucco, Anna Simona
Nico, Andrea
Albanesi, Marcello
Giliberti, Lucia
D'Elia, Luciana
Caiaffa, Maria Filomena
Macchia, Luigi - Abstract:
- Abstract: Background: Randomized Controlled Trials showed that omalizumab exhibited a good safety and tolerability profile in patients with moderate-to-severe asthma. However, safety data of long-term treatment with omalizumab are scarce. Our aim was to assess the safety of omalizumab in patients under long-term treatment in a real-life setting. Methods: Difficult-to-control asthmatic patients treated with omalizumab up to 9 years were retrospectively evaluated. Mild to severe adverse events any and reasons for discontinuation were recorded. Results: Ninety-one patients (26.4% males, mean age 49.9 ± 14.9 years) were included: mean treatment length, 3.8 ± 2.6 years; mean individual monthly dose, 514.5 ± 345.7 mg (range, 150–1200 mg). A total of 10, 472 single injections were given cumulatively to the 91 patients (115 single injections per patients, on average, over a treatment period up to 9 years). Fifty-nine patients (64.8%) were treated for a period of time from 3 to 9 years, 14 of whom from 6 to 9 years. A high proportion of patients who discontinued treatment dropped out within the first year (18, 39.1%), mainly for reasons unrelated to treatment. Six patients (6.6%) discontinued omalizumab for treatment-related adverse events: arthralgia/myalgia (3 patients); urticaria, angioedema (1 patients); metrorrhagia (1 patient); relapsing herpes labialis (1 patient). Four other patients complained of mild adverse events (rhinitis/conjunctivitis, injection site reaction, fatigue,Abstract: Background: Randomized Controlled Trials showed that omalizumab exhibited a good safety and tolerability profile in patients with moderate-to-severe asthma. However, safety data of long-term treatment with omalizumab are scarce. Our aim was to assess the safety of omalizumab in patients under long-term treatment in a real-life setting. Methods: Difficult-to-control asthmatic patients treated with omalizumab up to 9 years were retrospectively evaluated. Mild to severe adverse events any and reasons for discontinuation were recorded. Results: Ninety-one patients (26.4% males, mean age 49.9 ± 14.9 years) were included: mean treatment length, 3.8 ± 2.6 years; mean individual monthly dose, 514.5 ± 345.7 mg (range, 150–1200 mg). A total of 10, 472 single injections were given cumulatively to the 91 patients (115 single injections per patients, on average, over a treatment period up to 9 years). Fifty-nine patients (64.8%) were treated for a period of time from 3 to 9 years, 14 of whom from 6 to 9 years. A high proportion of patients who discontinued treatment dropped out within the first year (18, 39.1%), mainly for reasons unrelated to treatment. Six patients (6.6%) discontinued omalizumab for treatment-related adverse events: arthralgia/myalgia (3 patients); urticaria, angioedema (1 patients); metrorrhagia (1 patient); relapsing herpes labialis (1 patient). Four other patients complained of mild adverse events (rhinitis/conjunctivitis, injection site reaction, fatigue, thrombosis) but continued the treatment. Anaphylaxis was not reported. Conclusions: Long-term treatment with omalizumab appears remarkably safe and well tolerated in real-life setting. Prolonged omalizumab treatment for many consecutive years did not increase the risk of side effects, particularly anaphylaxis. Highlights: Long-term treatment with omalizumab is remarkably safe and well tolerated. Prolonging omalizumab for many years does not increase the risk of side effects. The risk of anaphylaxis is extremely low. The majority of patients discontinue omalizumab for reason other than adverse events. … (more)
- Is Part Of:
- Respiratory medicine. Volume 130(2017)
- Journal:
- Respiratory medicine
- Issue:
- Volume 130(2017)
- Issue Display:
- Volume 130, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 130
- Issue:
- 2017
- Issue Sort Value:
- 2017-0130-2017-0000
- Page Start:
- 55
- Page End:
- 60
- Publication Date:
- 2017-09
- Subjects:
- Monoclonal antibodies -- IgE -- Drop-out -- Adverse events -- Side effects
Chest -- Diseases -- Periodicals
Chest -- Diseases -- Great Britain -- Periodicals
Respiratory organs -- Diseases -- Periodicals
Respiratory Tract Diseases -- Periodicals
Appareil respiratoire -- Maladies -- Périodiques
Thorax -- Maladies -- Périodiques
Appareil respiratoire -- Maladies -- Traitement -- Périodiques
Electronic journals
616.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09546111 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/09546111 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/09546111 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.rmed.2017.07.013 ↗
- Languages:
- English
- ISSNs:
- 0954-6111
- Deposit Type:
- Legaldeposit
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