Abstract
Purpose of Review: Since omalizumab has been approved for urticaria, numerous randomized and real-life observational trials have been published. We reviewed the period January 2017–February 2018. Recent Findings: Omalizumab is effective for the control of urticaria recalcitrant to antihistamines in different populations globally. The ratio of total serum IgE 4-week/baseline ≥2 can predict response with a high likelihood. In observational real-life trials, doses have been adjusted on an individual basis: in some populations, up to two-thirds of the patients can be controlled with 150 mg/month; however, others are still not controlled with 300 mg/month. In these, 150 mg bimonthly could be tried, before up-dosing to 450 mg/month. On the long run (up to 3 years) omalizumab kept its efficacy. In many patients, dosing intervals could be augmented (6–8 weeks, some even more). After a 12-month treatment, about 20% showed long-term remission without relapse. Summary: Some biomarkers are being detected. Adjusting omalizumab doses in urticaria patients could enhance efficacy (shortening dosing interval and/or augmenting dose) and save costs (after 12 months: extending dosing interval and/or reducing dose).
| Original language | English |
|---|---|
| Article number | 33 |
| Journal | Current Allergy and Asthma Reports |
| Volume | 18 |
| Issue number | 5 |
| DOIs | |
| State | Published - 1 May 2018 |
Keywords
- Adverse events
- Chronic inducible urticaria
- Chronic spontaneous urticaria
- Dosing intervals
- Omalizumab
- Pregnancy
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