New England Journal of Medicine· 2013Q1
Antihistaminiklere Yanıt Vermeyen Kronik İdiyopatik Ürtiker Tedavisinde Omalizumab
Omalizumab for the Treatment of Chronic Idiopathic or Spontaneous Urticaria
- 1.080atıf
- Q1SCImago
- 2013yıl
Kısa özet
Anti-IgE antikoru olan omalizumab, standart antihistaminik dozlarına yanıt vermeyen kronik idiyopatik ürtiker hastalarında kaşıntı şiddetini önemli ölçüde azaltmıştır.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Ana noktalar
- Omalizumab, antihistaminiklere yanıt vermeyen kronik idiyopatik ürtiker hastalarında kaşıntı şiddetini anlamlı derecede azaltmıştır.
- Omalizumab'ın 300 mg dozu, plaseboya (-5.1) kıyasla 12. haftada en büyük ortalama kaşıntı şiddeti skoru düşüşünü (-9.8) sağlamıştır.
- 150 mg (P=0.001) ve 300 mg (P<0.001) omalizumab dozlarında 12. haftada anlamlı iyileşmeler gözlenmiştir.
- Plasebo, 75 mg, 150 mg ve 300 mg omalizumab grupları arasında yan etki sıklıkları benzerdi.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Özet (abstract)
BACKGROUND: Many patients with chronic idiopathic urticaria (also called chronic spontaneous urticaria) do not have a response to therapy with H-antihistamines, even at high doses. In phase 2 trials, omalizumab, an anti-IgE monoclonal antibody [corrected] that targets IgE and affects mast-cell and basophil function, has shown efficacy in such patients. METHODS: In this phase 3, multicenter, randomized, double-blind study, we evaluated the efficacy and safety of omalizumab in patients with moderate-to-severe chronic idiopathic urticaria who remained symptomatic despite H-antihistamine therapy (licensed doses). We randomly assigned 323 patients to receive three subcutaneous injections, spaced 4 weeks apart, of omalizumab at doses of 75 mg, 150 mg, or 300 mg or placebo, followed by a 16-week observation period. The primary efficacy outcome was the change from baseline in a weekly itch-severity score (ranging from 0 to 21, with higher scores indicating more severe itching). RESULTS: The baseline weekly itch-severity score was approximately 14 in all four study groups. At week 12, the mean (±SD) change from baseline in the weekly itch-severity score was -5.1±5.6 in the placebo group, -5.9±6.5 in the 75-mg group (P=0.46), -8.1±6.4 in the 150-mg group (P=0.001), and -9.8±6.0 in the 300-mg group (P<0.001). Most prespecified secondary outcomes at week 12 showed similar dose-dependent effects. The frequency of adverse events was similar across groups. The frequency of serious adverse events was low, although the rate was higher in the 300-mg group (6%) than in the placebo group (3%) or in either the 75-mg or 150-mg group (1% for each). CONCLUSIONS: Omalizumab diminished clinical symptoms and signs of chronic idiopathic urticaria in patients who had remained symptomatic despite the use of approved doses of H-antihistamines. (Funded by Genentech and Novartis Pharma; ClinicalTrials.gov number, NCT01292473.).
Yazarların özeti; kaynağından alınmıştır. New England Journal of Medicine, 2013 · DOI ↗
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