March 2012
Volume 53, Issue 14
Free
ARVO Annual Meeting Abstract  |   March 2012
Combined Inhibition of Tumor Necrosis Factor (TNF) and Vascular Endothelial Growth Factor (VEGF) for the Treatment of Macular Edema of Various Etiologies: A Short-term Pilot Study
Author Affiliations & Notes
  • Martin A. Serrano
    Retina and Vitreous Service, Clinica Oftalmologica Centro Caracas, Caracas, Venezuela
  • Lihteh Wu
    Instituto de Cirugia Ocular, San Jose, Costa Rica
  • J. Fernando Arevalo
    Retina Division, Wilmer Eye Institute, Baltimore, Maryland
    Vitreoretinal Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia
  • Footnotes
    Commercial Relationships  Martin A. Serrano, None; Lihteh Wu, None; J. Fernando Arevalo, None
  • Footnotes
    Support  The Arevalo-Coutinho Foundation for Research in Ophthalmology, Caracas, Venezuela.
Investigative Ophthalmology & Visual Science March 2012, Vol.53, 904. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Martin A. Serrano, Lihteh Wu, J. Fernando Arevalo; Combined Inhibition of Tumor Necrosis Factor (TNF) and Vascular Endothelial Growth Factor (VEGF) for the Treatment of Macular Edema of Various Etiologies: A Short-term Pilot Study. Invest. Ophthalmol. Vis. Sci. 2012;53(14):904.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract
 
Purpose:
 

To report the 6-month anatomic and Early Treatment Diabetic Retinopathy Study (ETDRS) best-corrected visual acuity (BCVA) response after the combination of intravitreal adalimumab (Humira) and bevacizumab (Avastin) in patients with macular edema of various etiologies.

 
Methods:
 

Retrospective interventional case series. We reviewed the clinical records of 5 consecutive patients (7 eyes) with macular edema of various etiologies including pseudophakic macular edema, diabetic papillophlebitis, central retinal vein occlusion, branch retinal vein occlusion, and exudative age-related macular degeneration. All patients were treated with at least one intravitreal injection of 1.25 mg/0.05 mL of bevacizumab and 2 mg/0.08 mL of adalimumab . Patients underwent ETDRS BCVA testing, ophthalmoscopic examination, optical coherence tomography (OCT), and fluorescein angiography (FA) at baseline, 1-, 3- and 6-month visits. Main outcome measures included changes in BCVA, and OCT.

 
Results:
 

The mean age of our patients was 71.5 ± 9.4 years. The mean number of combined bevacizumab and adalimumab injections per eye was 2.14 (range: 1 to 4 injections) at 6 months. The baseline BCVA improved from 1.19 ± 0.6 logarithm of the minimum angle of resolution (logMAR) to 0.94 ± 0.59 logMAR at 6 months (P < 0.05). Four (57.1%) of seven eyes gained ≥ 3 ETDRS lines of BCVA. Central macular thickness (CMT) at baseline by OCT had a mean of 416 ± 150 µm which was reduced to a mean of 354 ± 205 µm at 6 months (P < 0.05). There were no ocular or systemic complications.

 
Conclusions:
 

Combined intravitreal bevacizumab at doses of 1.25 mg and adalimumab at doses of 2.0 mg seems to provide stability or improvement in BCVA, OCT, and FA in macular edema of various etiologies with no systemic complications at 6 months of follow up. Although limited by the small sample size, short follow-up, and lack of a control group, our results suggest potential bioactivity related to the favorable functional and anatomic outcome achieved.  

 
Keywords: macula/fovea • edema • clinical (human) or epidemiologic studies: treatment/prevention assessment/controlled clinical trials 
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×