Monday, September 19, 2005

News from The Retinal Society Meeting

News from The Retinal Society Meeting in San Diego
September 19, 2005

I just returned from the annual meeting of The Retinal Society in San Diego. The Society consists of an elected group of retinal specialists within ophthalmology. One of the main topics was the use of Avastin® intraocularly to treat the wet form of AMD. Let me recap the reasoning behind intraocular Avastin®:

In the July 19th blog I summarized the results from the MARINA Study that had just been announced at the meeting of the American Society of Retinal Specialists in Montreal. The MARINA Study tested the use of Lucentis® intraocularly for the treatment of the wet form of AMD. At 12 months, the patients who received Lucentis® gained 7 letters of vision compared to a loss of 10.5 letters in the control group. This 17 letter difference between the treatment and control groups represents over three lines on the visual acuity chart. In addition, forty percent of the patients who received Lucentis® had 20/40 or better vision at 12 months! This was the first treatment for the wet form of AMD that resulted in improved vision and the results were much better than the results for either Macugen® or Visudyne®.

Lucentis® is a smaller active molecule cleaved from the larger molecule, Avastin®. Genentech made the smaller molecule because they believed that Avastin® was too large to pass through the retina. Retinal specialists were frustrated because some of their patients were not responding well to Visudyne® or Macugen® and because Lucentis® is not yet FDA approved. So they tried Avastin®. Intravenous Avastin® worked very well for treating the wet form of AMD but has some potential severe side-effects such as stokes and heart attacks so a few retinal specialists injected much smaller amounts of Avastin® directly into the eye.
So far, probably about 500 patients with the wet form of AMD have received injections of Avastin®. Intraocular Avastin® appears to work very well at stopping the growth and leakage of the new blood vessels in wet AMD. There have been no signs of toxicity or side-effects but most of these patients have been followed for only a few months. Most retinal specialists recommend Avastin® only after Visudyne® or Macugen® treatments, both of which are approved by the FDA, have failed to control the new blood vessels.

What should you do now if you have or know someone who has wet AMD? I think an initial treatment with Visudyne® or Macugen® is reasonable. Usually an injection of intraocular Kenalog® is given with Visudyne® because it appears to improve the prognosis. If this initial treatment doesn’t work, say after one Visudyne® treatment or two injections of Macugen®, I think it would be reasonable to talk to your doctor about Avastin®.
This is what we know as of September 19, 2005. We will learn much more in the next year as patients are followed for longer periods of time and from the many clinical trials that are being performed on wet AMD.

Please stay in touch to keep up to date. As always, I welcome your questions.

1 Comments:

Blogger Susan M. Malinowski, MD said...

Jim,

Hello and thanks for the info.

Can you provide any additional information...have you used Avastin intraocularly? How much? How often?

At the Retina Society, how many patients were injected, over what period of time was the follow up? What types of neovascularization were treated?

Thanks so much!

Susan Malinowski, MD

3:13 PM  

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