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Update on Omalizumab for Urticaria: What’s New in the Literature from Mechanisms to Clinic

  • Désirée E.S. Larenas-Linnemann
  • , Claudio A.S. Parisi
  • , Carla Ritchie
  • , Ricardo Cardona-Villa
  • , Ivan Cherrez-Ojeda
  • , Annia Cherrez
  • , Luis Felipe Ensina
  • , Elizabeth Garcia
  • , Iris V. Medina
  • , Mónica Rodríguez-González
  • , Jorge Mario Sánchez Caraballo

Research output: Contribution to journalReview articlepeer-review

29 Scopus citations

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 languageEnglish
Article number33
JournalCurrent Allergy and Asthma Reports
Volume18
Issue number5
DOIs
StatePublished - 1 May 2018

Keywords

  • Adverse events
  • Chronic inducible urticaria
  • Chronic spontaneous urticaria
  • Dosing intervals
  • Omalizumab
  • Pregnancy

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