New England Journal of Medicine· 2015Q1· Klinik çalışma
Diyabetik Maküler Ödem İçin Aflibersept, Bevasizumab veya Ranibizumab
Aflibercept, Bevacizumab, or Ranibizumab for Diabetic Macular Edema
- 1.586atıf
- Q1SCImago
- 2015yıl
Kısa özet
Göz içi aflibersept, bevasizumab ve ranibizumab, diyabetik maküler ödem hastalarında görmeyi iyileştirdi, ancak aflibersept yalnızca başlangıçta daha kötü görme keskinliğine sahip gözlerde daha fazla etkinlik gösterdi.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Ana noktalar
- Aflibersept, başlangıç görme keskinliği 69'un altında (yaklaşık 20/50 veya daha kötü) olan gözlerde, bevasizumab ve ranibizmaba kıyasla daha üstün görme keskinliği iyileşmesi gösterdi.
- Daha hafif görme bozukluğu olan gözlerde (başlangıç harf puanı 69-78), üç ilaç arasında görme iyileşmesinde anlamlı farklar bulunmadı.
- Çalışmaya 89 klinik siteden 660 yetişkin katıldı ve rastgele aflibersept, bevasizumab veya ranibizumab tedavisi aldı.
- Tedavi grupları arasında ciddi yan etkiler, hastaneye yatış, ölüm veya majör kardiyovasküler olay oranlarında anlamlı farklar bulunmadı.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Özet (abstract)
BACKGROUND: The relative efficacy and safety of intravitreous aflibercept, bevacizumab, and ranibizumab in the treatment of diabetic macular edema are unknown. METHODS: At 89 clinical sites, we randomly assigned 660 adults (mean age, 61±10 years) with diabetic macular edema involving the macular center to receive intravitreous aflibercept at a dose of 2.0 mg (224 participants), bevacizumab at a dose of 1.25 mg (218 participants), or ranibizumab at a dose of 0.3 mg (218 participants). The study drugs were administered as often as every 4 weeks, according to a protocol-specified algorithm. The primary outcome was the mean change in visual acuity at 1 year. RESULTS: From baseline to 1 year, the mean visual-acuity letter score (range, 0 to 100, with higher scores indicating better visual acuity; a score of 85 is approximately 20/20) improved by 13.3 with aflibercept, by 9.7 with bevacizumab, and by 11.2 with ranibizumab. Although the improvement was greater with aflibercept than with the other two drugs (P<0.001 for aflibercept vs. bevacizumab and P=0.03 for aflibercept vs. ranibizumab), it was not clinically meaningful, because the difference was driven by the eyes with worse visual acuity at baseline (P<0.001 for interaction). When the initial visual-acuity letter score was 78 to 69 (equivalent to approximately 20/32 to 20/40) (51% of participants), the mean improvement was 8.0 with aflibercept, 7.5 with bevacizumab, and 8.3 with ranibizumab (P>0.50 for each pairwise comparison). When the initial letter score was less than 69 (approximately 20/50 or worse), the mean improvement was 18.9 with aflibercept, 11.8 with bevacizumab, and 14.2 with ranibizumab (P<0.001 for aflibercept vs. bevacizumab, P=0.003 for aflibercept vs. ranibizumab, and P=0.21 for ranibizumab vs. bevacizumab). There were no significant differences among the study groups in the rates of serious adverse events (P=0.40), hospitalization (P=0.51), death (P=0.72), or major cardiovascular events (P=0.56). CONCLUSIONS: Intravitreous aflibercept, bevacizumab, or ranibizumab improved vision in eyes with center-involved diabetic macular edema, but the relative effect depended on baseline visual acuity. When the initial visual-acuity loss was mild, there were no apparent differences, on average, among study groups. At worse levels of initial visual acuity, aflibercept was more effective at improving vision. (Funded by the National Institutes of Health; ClinicalTrials.gov number, NCT01627249.).
Yazarların özeti; kaynağından alınmıştır. New England Journal of Medicine, 2015 · DOI ↗
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OphthalmologyMedicine