Photodynamic therapy with verteporfin for choroidal neovascularization caused by age-related macular degeneration: results of a single treatment in a phase 1 and 2 study.

OBJECTIVE To evaluate the safety and short-term visual and fluorescein angiographic effects of a single photodynamic therapy treatment with verteporfin with the use of different dosage regimens in patients with choroidal neovascularization (CNV) from age-related macular degeneration. DESIGN Nonrandomized, multicenter, open-label, clinical trial using 5 dosage regimens. SETTING Four ophthalmic centers in North America and Europe providing retinal care. PARTICIPANTS Patients with subfoveal CNV caused by age-related macular degeneration. METHODS Standardized protocol refraction, visual acuity testing, ophthalmic examination, color photographs, and fluorescein angiograms were used to evaluate the effects of a single treatment of photodynamic therapy with verteporfin. Follow-up was planned through 3 months in 97 patients and for less than 3 months in 31 other patients. RESULTS The mean visual acuity change (and range of change) from baseline at the follow-up examination at week 12 after a single treatment with regimens 1 through 5 was -0.2 (-3 to +2), -0.9 (-9 to +5), -1.6 (-9 to +2), +0.4 (-8 to +7), and +0.1 (-8 to +9) lines, respectively. Only the highest light dose (150 J/cm2) in regimens 2 and 3, which produced angiographic nonperfusion of neurosensory retinal vessels, caused marked vision loss. Some cessation of fluorescein leakage from CNV was achieved without loss of vision when the light dose used was less than 150 J/cm2. Systemic adverse events were rare. Cessation of fluorescein leakage from CNV was noted in all regimens by 1 week after photodynamic therapy. Fluorescein leakage from at least a portion of the CNV reappeared by 4 to 12 weeks after treatment in almost all cases. Progression of classic CNV beyond the area of CNV identified before treatment was noted in 42 (51%) of the 83 eyes with classic CNV followed up for 3 months after a single treatment. Eyes in which the area of any CNV leakage at 12 weeks was less than at baseline had a significantly better visual acuity outcome (+0.8 line) than eyes in which CNV leakage progressed (-0.8 line). CONCLUSIONS Photodynamic therapy with verteporfin achieved short-term cessation of fluorescein leakage from CNV without loss of vision or growth of classic CNV in some patients with age-related macular degeneration. Except for nonperfusion of neurosensory retinal vessels at a light dose of 150 J/cm2, no other adverse events were of concern. Randomized clinical trials to investigate whether this new modality can preserve vision in patients with CNV secondary to age-related macular degeneration are justified.

[1]  Johannes R. Vingerling,et al.  The prevalence of age-related maculopathy in the Rotterdam Study. , 1995, Ophthalmology.

[2]  A. Jain,et al.  Photosensitising potency of structural analogues of benzoporphyrin derivative (BPD) in a mouse tumour model. , 1991, British Journal of Cancer.

[3]  Persistent and recurrent neovascularization after krypton laser photocoagulation for neovascular lesions of age-related macular degeneration. Macular Photocoagulation Study Group. , 1990, Archives of ophthalmology.

[4]  B. Bengtsson,et al.  DISC HAEMORRHAGE AND GLAUCOMA , 1981, Acta ophthalmologica.

[5]  J Flammer,et al.  Quantification of glaucomatous visual field defects with automated perimetry. , 1985, Investigative ophthalmology & visual science.

[6]  R Birngruber,et al.  Photodynamic therapy with verteporfin for choroidal neovascularization caused by age-related macular degeneration: results of retreatments in a phase 1 and 2 study. , 1999, Archives of ophthalmology.

[7]  A. Sommer,et al.  Prevalence and significance of optic disc hemorrhage in a longitudinal study of glaucoma. , 1990, Archives of ophthalmology.

[8]  C. Krakau,et al.  REGRESSION ANALYSIS OF THE CENTRAL VISUAL FIELD IN CHRONIC GLAUCOMA CASES , 1982, Acta ophthalmologica.

[9]  E. Gramer,et al.  Quantifizierung und Progredienz des Gesichtsfeldschadens bei Glaukom ohne Hochdruck, Glaucoma simplex und Pigmentglaukom* , 1987 .

[10]  A. Richter,et al.  THE EFFECTS OF PLASMA LIPOPROTEINS ON in vitro TUMOR CELL KILLING and in vivo TUMOR PHOTOSENSITIZATION WITH BENZOPORPHYRIN DERIVATIVE , 1991, Photochemistry and photobiology.

[11]  R. Klein,et al.  Prevalence of age-related maculopathy. The Beaver Dam Eye Study. , 1992, Ophthalmology.

[12]  J. Katz,et al.  Analysis of progressive change in automated visual fields in glaucoma. , 1996, Investigative ophthalmology & visual science.

[13]  R Birngruber,et al.  Photodynamic therapy of experimental choroidal melanoma using lipoprotein-delivered benzoporphyrin. , 1994, Ophthalmology.

[14]  D. Dolphin,et al.  Biodistribution of tritiated benzoporphyrin derivative (3H-BPD-MA), a new potent photosensitizer, in normal and tumor-bearing mice. , 1990, Journal of photochemistry and photobiology. B, Biology.

[15]  S. W. Siegner,et al.  Optic disc hemorrhages and progression of glaucoma. , 1996, Ophthalmology.

[16]  F. Ferris,et al.  New visual acuity charts for clinical research. , 1982, American journal of ophthalmology.

[17]  Erik L. Greve,et al.  Some Possibilities of the Peritest Automatic and Semi-Automatic Perimeter , 1983 .

[18]  U. Schmidt-Erfurth,et al.  In vivo uptake of liposomal benzoporphyrin derivative and photothrombosis in experimental corneal neovascularization , 1995, Lasers in surgery and medicine.

[19]  Joan W. Miller,et al.  Liposomal benzoporphyrin derivative verteporfin photodynamic therapy. Selective treatment of choroidal neovascularization in monkeys. , 1996, Ophthalmology.

[20]  S. Drance,et al.  The rate of progression of scotomas in glaucoma. , 1986, American journal of ophthalmology.

[21]  T J Flotte,et al.  Photodynamic therapy of experimental choroidal neovascularization using lipoprotein-delivered benzoporphyrin. , 1995, Archives of ophthalmology.

[22]  R. Hitchings,et al.  The Nature of Visual Loss in Low Tension Glaucoma , 1985 .

[23]  E. Gragoudas,et al.  Photodynamic therapy of pigmented choroidal melanomas using a liposomal preparation of benzoporphyrin derivative. , 1996, Archives of ophthalmology.

[24]  H A Quigley,et al.  A comparison of Peritest automated perimetry and Goldmann perimetry. , 1985, Archives of ophthalmology.

[25]  F L Ferris,et al.  Senile macular degeneration: a case-control study. , 1983, American journal of epidemiology.

[26]  J L Jay,et al.  The rate of visual field loss in untreated primary open angle glaucoma. , 1993, The British journal of ophthalmology.

[27]  David A. Dewey,et al.  Corneal and retinal energy density with various laser beam delivery systems and contact lenses , 1991, Photonics West - Lasers and Applications in Science and Engineering.

[28]  T J Dougherty,et al.  Identification of singlet oxygen as the cytotoxic agent in photoinactivation of a murine tumor. , 1976, Cancer research.

[29]  Joan W. Miller,et al.  Intravenous infusion of liposomal benzoporphyrin derivative for photodynamic therapy of experimental choroidal neovascularization. , 1996, Archives of ophthalmology.

[30]  C. Zhou,et al.  Mechanisms of tumor necrosis induced by photodynamic therapy. , 1989, Journal of photochemistry and photobiology. B, Biology.

[31]  B. Bengtsson,et al.  The effect of perimetric experience in patients with glaucoma. , 1996, Archives of ophthalmology.

[32]  E. Gragoudas,et al.  Photodynamic therapy and digital angiography of experimental iris neovascularization using liposomal benzoporphyrin derivative. , 1997, Ophthalmology.

[33]  A. Sommer,et al.  Estimating progression of visual field loss in glaucoma. , 1997, Ophthalmology.

[34]  L. Herndon,et al.  Rate of progression in open-angle glaucoma estimated from cross-sectional prevalence of visual field damage. , 1997, American journal of ophthalmology.

[35]  D. C. Wu,et al.  Intraocular pressure and the rate of visual field loss in chronic open-angle glaucoma. , 1991, American journal of ophthalmology.

[36]  R Birngruber,et al.  Vascular targeting in photodynamic occlusion of subretinal vessels. , 1994, Ophthalmology.

[37]  Joan W. Miller,et al.  Effects of photodynamic therapy using verteporfin on experimental choroidal neovascularization and normal retina and choroid up to 7 weeks after treatment. , 1999, Investigative ophthalmology & visual science.

[38]  B. Becker,et al.  The onset and evolution of glaucomatous visual field defects. , 1982, Ophthalmology.

[39]  E. Werner,et al.  Effect of patient experience on the results of automated perimetry in clinically stable glaucoma patients. , 1988, Ophthalmology.

[40]  S. Drance,et al.  Disc hemorrhages in the glaucomas. , 1989, Survey of ophthalmology.

[41]  S M Drance,et al.  The mode of progression of visual field defects in glaucoma. , 1984, American journal of ophthalmology.

[42]  F. Ferris,et al.  Age-related macular degeneration and blindness due to neovascular maculopathy. , 1984, Archives of ophthalmology.