11 articles, page 2 of 11

Review article

The Treatment of Wet Age-Related Macular Degeneration

Dtsch Arztebl Int 2009; 106(18): 312-7; DOI: 10.3238/arztebl.2009.0312

Joussen, A M; Bornfeld, N

Augenklinik der Universität Düsseldorf: Prof. Dr. med. Joussen
Abteilung hinterer Augenabschnitt, Augenklinik der Universität Essen: Prof. Dr. med. Bornfeld
Background: Age-related macular degeneration (AMD) is a progressive disease affecting the macula, the area of the retina that has the highest visual acuity. It can progress to geographic atrophy or choroidal neovascularization.
Method: Selective literature review.
Results: The authors discuss the results of therapeutic trials and the treatment recommendations of the ophthalmological societies. Mechanism-targeted treatments and improved modes of administration offer the potential for improved therapy.
Conclusions: With the advent of the antivascular endothelial growth factor (anti-VEGF) therapy, the prognosis of choroidal neovascularization has changed dramatically. Visual acuity can actually be improved, but, in most cases, the improvement can only be sustained with repeated intravitreal injections.
Dtsch Arztebl Int 2009; 106(18): 312–7
DOI: 10.3238/arztebl.2009.0312
Key words: macular degeneration, age-related macular degeneration, off-label treatment, treatment, monoclonal antibodies
The use of vascular endothelial growth factor (VEGF) inhibitors to treat age-related macular degeneration has been widely covered in the press and has generated much public discussion, in which highly subjective points of view are often expressed (1). This article is a selective review of the literature based on a PubMed search for the terms "age-related macular degeneration" and "therapy" as well as on the current health policy debate over this matter in Germany (e1).

Age-related macular degeneration is the most common cause of blindness in the elderly (2, e2). Although only a minority of patients with late age-related macular degeneration (AMD) lose enough visual acuity to qualify as legally blind (see table 1 gif ppt) (e3), most patients with advanced AMD have only poor residual vision and thus meet the definition of "severe visual impairment" currently in use in Germany (table 1). Exudative, or "wet," AMD is a late form of AMD (as distinguished from atrophic, so-called dry, AMD) and is responsible for 60% to 80% of all cases of blindness due to AMD. The prevalence of advanced AMD is estimated at 1.47% in the United States population (e4). An extrapolation to Europe yields a prevalence figure of 3.5% among persons over age 65 (3).

The cells of the retinal pigment epithelium (RPE) play a central role in the pathogenesis of age-related macular degeneration. They are responsible for the generation and maintenance of the extracellular matrix, the photoreceptor matrix, and the membrane of Bruch, as well as for ion and fluid transport between the photoreceptors and the choroid membrane and for phagocytosis in the external segments of the photoreceptors. If these cells do not function properly, lipids and proteins accumulate in the area of Bruch's membrane, and Drusen are formed (4, 5).

The wet type of macular degeneration arises in only about 10% of all patients, among whom the main cause of blindness is neovascularization. Angiography permits various subtypes to be distinguished from one another; these subtypes are histologically characterized by vascular growth above or below Bruch's membrane. The terms that were originally introduced to distinguish them—"subfoveal," "subfoveolar," "juxtafoveal," and "extrafoveal"—are not now used in any uniform way. It is best, therefore, to draw only a single distinction between subfoveal, i.e., choroidal, neovascularization (CNV), which has not yet reached the avascular zone of the fovea, on the one hand and non-subfoveal membranes on the other (6, 7). Choroidal anastomoses and pigment epithelium detachments are special, distinguishable subtypes (e5).

Dry age-related macular degeneration is mainly treated with medical dietary supplementation (e7), although a number of surgical options are currently under investigation (e6). In contrast, the treatment options for the wet form of the condition have been markedly expanded in recent years by the introduction of anti-VEGF medications. This type of anti-angiogenic therapy is the first effective treatment offering not merely a slowing of the natural progression of the disease, but actually an improvement of visual acuity (6, e8).

Thermal photocoagulation
Thermal coagulation with the argon ("hot") laser is beneficial for patients with an exclusively extrafoveal membrane, i.e., one lying outside the avascular zone of the fovea (e9); this is the case in only about 5% of all patients. Thermal coagulation produces a scar that goes through all layers of the retina and that manifests itself clinically as a visual field defect. Therefore, the use of this treatment is restricted to the extrafoveal area. It is associated with a rather high recurrence rate (almost 50%).

Photodynamic therapy
Photodynamic therapy (PDT) with verteporfin has been tested in a number of prospective studies for the treatment of various subtypes of exudative, subfoveal AMD (8, e10). In 2000, the United States Food and Drug Administration (FDA) approved PDT with verteporfin for the treatment of predominantly classic, subfoveal choroidal neovascularization. Since then, many international studies have followed, investigating the potential indications of the technique in subtypes of wet age-related macular degeneration, in pathological myopia, and (in smaller studies) in choroidal neovascularization of other causes (e11, e12). Nonetheless, statutory health insurance in Germany no longer reimburses this form of treatment for occult membranes (e12). The latest recommendations of the German Ophthalmological Society classify PDT as a second-line treatment after the anti-VEGF therapies. Nonetheless, in certain cases, PDT can still play a useful role in combination therapy, in addition to growth factor inhibitors.

Treatment with VEGF inhibitors
The idea of a growth factor for blood vessels was first proposed by Michelson in 1948. Folkman and his research team, in the early 1970's, were able to show that tumor growth is closely related to the growth of tumor vessels, which, in turn, depends on the expression of special growth factors (9). Overexpression of vascular endothelial growth factor (VEGF) is considered to be the cause of choroidal neovascularization (10, e13). This growth factor selectively influences the growth of endothelial cells; in particular, it is responsible for vascular leakage, i.e., the pathological egress of fluid from the interior of blood vessels (e14).

The treatment of wet macular degeneration with anti-VEGF substances can be considered a milestone. Now, for the first time, an opportunity exists to treat neovascularization more directly and to inhibit it selectively.

Three medications of this type are currently in use:

- pegaptanib,
- ranibizumab, and
- bevacizumab.

Pegaptanib is an aptamer, i.e., a low-molecular-weight receptor molecule that captures bioactive VEGF before it has a chance to exert an effect on the cell. It inhibits only the VEGF 165 isoform, and none of the others. The effectiveness of treatment with pegaptanib has been demonstrated in phase III clinical trials, e.g., the VISION study (11, 12).

If pegaptanib is discontinued after one year of treatment, further growth of CNV is frequently observed. Continuous treatment for two years is significantly more effective, particularly in patients with early lesions of exudative AMD (e15, e16).

The positive results of prospective, randomized phase III trials led the FDA to approve pegaptanib on 17 December 2004 for the treatment of various subtypes of neovascular age-related macular degeneration (e15). The European Medicines Agency (EMEA) approved pegaptanib for use in the European Union on 31 January 2006, and the drug has been available in Germany since May 2006. Because the study findings to date have shown that pegaptanib can do no better than to stabilize (rather than improve) the patient's visual acuity, the German Ophthalmological Society recommends it only as a second-line treatment. It cannot yet be judged whether better results might be obtained by combining pegaptanib with PDT or with other VEGF inhibitors (e17).

Ranibizumab is a humanized monoclonal antibody fragment (Fab fragment; antigen-binding fragment) that binds all isoforms of VEGF-A. It inhibits the growth of CNV membranes, as well as CNV-induced macular edema. The studies that have been published to date show a better therapeutic effect for ranibizumab than for the aptamer pegaptanib.

12- and 24-month results are not yet available from two phase III trials (13, 14) in which ranibizumab was injected into the vitreous body at four-week intervals.

In the MARINA study, in which ranibizumab was used to treat minimal classic or occult CNV in 716 patients, more than 90% of the treated patients had a significantly improved visual acuity at both 12 and 24 months after the start of treatment (14).

Similarly, in the ANCHOR study, in which ranibizumab was used to treat 423 patients with predominantly classic CNV, about 95% of the treated patients had lost fewer than three lines of visual acuity in 12 months (three lines = significant loss of acuity), compared to 64% of the patients who had received PDT with verteporfin (13).

Ranibizumab is the first treatment for neovascular AMD with an approved medication (approval in January 2007) that can improve the patient's visual acuity. In the United States, monthly administration of ranibizumab is recommended; in contrast, the physicians' information sheet (Summary of Product Characteristics [SPC]) issued after the approval of the drug in Europe recommends an initial loading with three injections, followed by individually tailored maintenance therapy based on the course of the patient's visual acuity (Novartis information for physicians) (table 2 gif ppt).

Less common applications of this drug are under study in three clinical trials that are currently in progress (PIER, PrONTO, and SAILOR). The preliminary findings of the PrONTO trial suggest that less frequent injections can produce similar results to those obtained in the published phase III studies (e18), yet preliminary findings of the PIER trial suggest that lengthening the interval between injections leads to a worse result (e19). In view of its proven ability to improve visual acuity, ranibizumab has been recommended as a treatment for neovascular macular degeneration both by the scientific ophthalmological societies and by the German Association of Ophthalmologists.

Bevacizumab is a humanized complete antibody directed against VEGF-A and is closely related to the antibody fragment ranibizumab (e20). It has now been shown that the larger molecule bevacizumab completely penetrates the retina and choroid membrane after intravitreous application (15, e21).

Bevacizumab is recommended, in combination with cisplatin and paclitaxel, as the first line of therapy for patients with metastatic colorectal carcinoma and in subgroups of patients with advanced, metastatic carcinoma of the lung. In 2007, it was approved in Europe for the treatment of renal and breast cancer as well.

The use of bevacizumab for the treatment of intraocular retinal and choroidal neovascularization has been studied to date in a wide variety of clinical trials, most of them without a control group (16, e22, e23). The positive findings are comparable overall with the improvement of visual acuity achieved in the MARINA and ANCHOR trials after a few months' treatment with ranibizumab. As far as can be judged from the published data, there is no evidence for any major difference in the effect of bevacizumab against various angiographically distinguishable membrane subtypes (e24). Even though meta-analyses have yielded a judgment that bevacizumab is, in all probability, not inferior to ranibizumab, any potential difference cannot be definitively assessed till data are available from a prospective, randomized comparative trial (17).

The intravitreous application of bevacizumab lies outside the indications for which this drug has been approved and thus constitutes off-label use (table 3 gif ppt).

The safety of treatment with anti-VEGF medications
The reported side effects of anti-VEGF medications given intravenously at high doses for oncological indications include medically manageable hypertension (hypertensive crisis, 1.6%) and thromboembolism, the risk of which increases with age (up to 4.4%).

Neovascular, age-related macular degeneration is, among other things, a sign of vascular dysregulation. The combined risk of heart attack or stroke after intravitreous administration in the first year of the ANCHOR and MARINA trials was no different in the control groups and in the ranibizumab 0.3 mg groups (1.3% versus 1.6%). As in other studies, no difference was found at two years when higher doses were used (e25). Yet, in February 2007, the FDA observed critically that the rate of stroke in both dose arms of the SAILOR study was lower than that in the approval studies, but no corresponding mention of an elevated risk had been made in the drug information for physicians. This judgment resulted from a comparison of the incidence of stroke in the age group in which AMD typically appears with that in the treatment arms of the ranibizumab approval studies (e26).

There are no data from controlled studies with respect to the off-label intravitreous injection of bevacizumab. The results of 7113 injections in 5228 patients were analyzed on the basis of a questionnaire over the Internet: the rate of hypertension, transient ischemic attacks, and cerebrovascular accidents was no higher than 0.21% (18). There is no evidence to date suggesting that the systemic complications are any more common than those following the intravitreous application of ranibizumab.

It remains fundamentally true, however, that the systemic concentration of the drug might cause relevant changes in tissues outside its immediate area of application (e27).

Ocular side effects of injection, including corneal abrasion, damage to the lens, endophthalmitis, retinal detachment, or vascular occlusion, have been described for all of the medications that are in use, in roughly equal frequencies (19).

A specific complication (tearing of the pigment epithelium) that can permanently impair visual acuity has been observed after bevacizumab injections for the treatment of a specific subtype of wet macular degeneration (extensive pigment epithelium detachment) (19). Initial reports, however, reveal a comparable frequency of this complication after treatment with ranibizumab (20). In patients with preexisting pigment epithelium detachment, the treating physician should assess the risks and benefits carefully.

Further information on cost-effectiveness and off-label use can be found online (e-box gif ppt).

The duration of treatment
At first, three injections are recommended. If the initial effect of treatment is positive, further treatment should be given after the third injection in case the clinical examination and follow-up fluorescein angiography reveal disease progression (worsening of visual acuity, new hemorrhage[s] in the macula, increase or reactivation of macular edema and/or CNV). Even in the absence of relevant study data concerning the optimal duration of intravitreous injection therapy with any of the currently used anti-VEGF drugs, further treatment would seem not to be indicated if the visual acuity sinks below 0.05, or if extensive subretinal fibrosis or atrophy develops. Further treatment may be beneficial, however, when fresh hemorrhages have occurred at the periphery of the membranes.

In accordance with the guiding principles of treatment described above, the treatment should be terminated only if the above criteria for continuing therapy and for disease progression are not met after a temporary pause in the treatment, or if the clinical findings worsen substantially despite an uploading dose. Termination of treatment should also be considered if further treatment seems unlikely to stave off a loss of visual acuity, i.e., if functional and morphological end-stage disease is already present (6).

Alternative treatments
Combination therapy
The intravitreous administration of steroids alone can no longer be recommended, in view of the results of VEGF inhibitor treatment that are described here. Nonetheless, combined treatment appears to be a promising approach.

Case series and randomized studies have shown that PDT combined with intravitreous triamcinolone can stabilize visual acuity and prolong the interval between treatments (e30). Similarly, synergistic effects of bevacizumab and PDT have been described in a number of studies (8, e31). The FOCUS trial studied the combination of ranibizumab with PDT; according to the initial results, however, combined therapy was no better at improving visual acuity than ranibizumab alone, though it did seem to lower the frequency of injections.

It is clear that the potential benefit of triple combinations, such as a combination of PDT, triamcinolone, and pegaptanib (e31) or of PDT, intravitreous dexamethasone, and intraocular bevacizumab (e32), can only be definitively assessed with long-term studies. The results reported to date have not been confirmed in controlled trials.

Having seen the current possibilities for treatment with anti-VEGF drugs, one may well ask whether surgical methods have any role left to play. A comparison of the results of the Submacular Surgery Trial (SST) (21), or of rotation (e33) or patch translocation (i.e., transplantation of the choroid membrane and the pigment epithelium) (e6, e34), with the latest publications on pharmacotherapy indeed makes clear that medical treatment is vastly superior with respect to the improvement of visual acuity. Massive subretinal hemorrhage is a medically untreatable entity that will remain in the domain of surgical treatment.

Other types of pharmacotherapy
The number of angiostatic substances being tested in oncology today that might also be useful in the eye is already too large to be encompassed in a brief overview. The e-table (gif ppt) lists a selection of candidate substances that have already been tested in experimental models of ocular neovascularization or in clinical trials.

The potential for a substance that has been tested in the laboratory to be developed into a medical treatment is a function not only of its effectiveness at inhibiting angiogenesis in vitro and in vivo, but also of the degree to which it influences physiological mechanisms. It has been shown that VEGF and its receptors are expressed in the normal retina as well, and there is still no answer to the question whether inhibiting VEGF or other factors that are normally present might harm the functioning of neurons or other cells over the long term (22). The value of these novel types of therapy will thus depend, not just on their systemic risk profile, but also to a large extent on the changes they induce in the local microcosm of the retina.

The authors thank Dr. Ruth Kölb-Keerl, Düsseldorf, for many suggested improvements to the manuscript.

Conflict of Interest Statement
Professors Joussen and Bornfeld have received lecture fees and study support from Novartis Pharma.

Manuscript received on 25 February 2008; revised version accepted on
12 January 2009.

Translated from the original German by Ethan Taub, M.D.

Corresponding author
Prof. Dr. med. Antonia M. Joussen
Augenklinik der Universität Düsseldorf
Moorenstr. 5
40225 Düsseldorf
Spiro T: Luc(ifer)entis. Dtsch Arztebl 2007; 104(28–29): A2033. VOLLTEXT
Klein R, Wang Q, Klein BE, Moss SE, Meuer SM: The relationship of age-related maculopathy, cataract, and glaucoma to visual acuity. Invest Ophthalmol Vis Sci 1995; 36: 182–91. MEDLINE
Schrader WF: Altersbedingte Makuladegeneration: eine sozioökonomische Zeitbombe in unserer alternden Gesellschaft. Ophthalmologe 2006; 103: 742–8. MEDLINE
Sarks SH, Arnold JJ, Killingsworth MC, Sarks JP: Early drusen formation in the normal and aging eye and their relation to age related maculopathy: a clinicopathological study. Br J Ophthalmol 1999; 83: 358–68. MEDLINE
de Jong PT: Age-related macular degeneration. N Engl J Med 2006; 355: 1474–85. MEDLINE
Pauleikhoff D, Bornfeld N, Gabel VP, Holz F, Roider H: Konsenspapier der Retinologischen Gesellschaft, der Deutschen Ophthalmologischen Gesellschaft und des Berufsverbandes der Augenärzte – Stellungnahme zur aktuellen Therapie der neovaskulären AMD. Klin Monatsbl Augenheilkd 2005; 222: 381–8. MEDLINE
Position of the Retinological Society, the German Ophthalmological Society and the Professional Association of Ophthalmologists in Germany on the current therapeutic possibilities for neovascular age-related macular degeneration. Klin Monatsbl Augenheilkd 2007; 224: 559–66. MEDLINE
Wormald R, Evans J, Smeeth L, Henshaw K: Photodynamic therapy for neovascular age-related macular degeneration. Cochrane Database Syst Rev. 2005 Oct 19; (4): CD002030. Review. Update in: Cochrane Database Syst Rev. 2007; (3): CD002030. MEDLINE
Folkman J: Anti-angiogenesis: new concept for therapy of solid tumors. Ann Surg 1972; 175: 409–16. MEDLINE
Miller JW, Adamis AP, Shima DT, D'Amore PA, Moulton RS et al.: Vascular endothelial growth factor/vascular permeability factor is temporally and spatially correlated with ocular angiogenesis in a primate model. Am J Pathol 1994; 145: 574–84. MEDLINE
Chakravarthy U, Adamis AP, Cunningham ET Jr. et al.: Year 2 efficacy results of 2 randomized controlled clinical trials of pegaptanib for neovascular age-related macular degeneration. Ophthalmology 2006; 113: 1508 e1–e25. MEDLINE
Jaissle GB, Szurman P, Bartz-Schmidt KU: Empfehlung für die Durchführung von intravitrealen Injektionen – Stellungnahme der Retinologischen Gesellschaft, der Deutschen Ophthalmologischen Gesellschaft (DOG) und des Berufsverbands der Augenärzte Deutschland (BVA). Klin Monatsbl Augenheilkd 2005; 222: 390–5. MEDLINE
Brown DM, Kaiser PK, Michels M et al.: Ranibizumab versus verteporfin for neovascular age-related macular degeneration. N Engl J Med 2006; 355: 1432–44. MEDLINE
Rosenfeld PJ, Brown DM, Heier JS et al.: Ranibizumab for neovascular age-related macular degeneration. N Engl J Med 2006; 355: 1419–31. MEDLINE
Heiduschka P, Fietz H, Hofmeister S et al.: Tübingen Bevacizumab Study Group: Penetration of bevacizumab through the retina after intravitreal injection in the monkey. Invest Ophthalmol Vis Sci 2007; 48: 2814–23. MEDLINE
Avery RL, Pieramici DJ, Rabena MD, Castellarin AA, Nasir MA, Giust MJ: Intravitreal bevacizumab (Avastin) for neovascular age-related macular degeneration. Ophthalmology 2006; 113: 363–72 e5. MEDLINE
Schouten JS, La Heij EC, Webers CA, Lundqvist IJ, Hendrikse F: A systematic review on the effect of bevacizumab in exudative age-related macular degeneration. Graefes Arch Clin Exp Ophthalmol 2009; 247: 1–11. MEDLINE
Fung AE, Rosenfeld PJ, Reichel E: The International Intravitreal Bevacizumab Safety Survey: using the internet to assess drug safety worldwide. Br J Ophthalmol 2006; 90: 1344–9. MEDLINE
Chan CK, Meyer CH, Gross JG et al.: Retinal pigment epithelial tears after intravitreal bevacizumab injection for neovascular age-related macular degeneration. Retina 2007; 27: 541–51. MEDLINE
Bakri SJ, Kitzmann AS: Retinal pigment epithelial tear after intravitreal ranibizumab. Am J Ophthalmol 2007; 143: 505–7. MEDLINE
Bressler SB, Childs AL, Haller JA et al.: Submacular Surgery Trials (SST) Research Group: Surgery for hemorrhagic choroidal neovascular lesions of age-related macular degeneration: ophthalmic findings: SST report no. 13. Ophthalmology 2004; 111: 1993–2006. MEDLINE
Kim I, Ryan AM, Rohan R et al.: Constitutive expression of VEGF, VEGFR-1, and VEGFR-2 in normal eyes. Invest Ophthalmol Vis Sci 1999; 40: 2115–21. Erratum in: Invest Ophthalmol Vis Sci 2000; 41: 368. MEDLINE
Lux A, Llacer H, Heussen FM, Joussen AM: Non-responders to bevacizumab (Avastin) therapy of choroidal neovascular lesions. Br J Ophthalmol 2007; 91: 1318–22. MEDLINE
PubMed-Suche 1998–2008; durchgeführt 8/2008.
Klaver CC, Wolfs RC, Vingerling JR, Hofman A, de Jong PT: Age-specific prevalence and causes of blindness and visual impairment in an older population: the Rotterdam Study. Arch Ophthalmol 1998; 116: 653–8. MEDLINE
Vinding T: Age-related macular degeneration. An epidemiological study of 1000 elderly individuals. With reference to prevalence, funduscopic findings, visual impairment and risk factors. Acta Ophthalmol Scand Suppl 1995; 217: 1–32. MEDLINE
Friedmann DS, O-Colmain BJ, Munoz B et al.: Eye Diseases Prevalence Research Group: Prevalence of age-related macular degeneration in the United States. Arch Ophthalmol 2004; 122: 564–72. MEDLINE
Joeres S, Heussen FM, Treziak T, Bopp S, Joussen AM: Bevacizumab (Avastin) treatment in patients with retinal angiomatous proliferation. Graefes Arch Clin Exp Ophthalmol 2007; 245: 1597–602. MEDLINE
Joussen AM, Joeres S, Fawzy N et al.: Autologous translocation of the choroid and retinal pigment epithelium in patients with geographic atrophy. Ophthalmology 2007; 114: 551–60. MEDLINE
Evans JR, Henshaw K: Antioxidant vitamin and mineral supplements for preventing age-related macular degeneration. Cochrane Database Syst Rev 2008; 1: CD000253. Review. MEDLINE
Vedula SS, Krzystolik MG: Antiangiogenic therapy with anti-vascular endothelial growth factor modalities for neovascular age-related macular degeneration. Cochrane Database Syst Rev 2008; 16: CD005139. MEDLINE
Macular Photocoagulation Study Group: Argon laser photocoagulation for senile macular degeneration. Five year results from randomized clinical trials. Arch Ophthalmol 1991; 109: 1109–14. MEDLINE
Treatment of Age-related Macular Degeneration with Photodynamic Therapy (TAP) Study Group. Photodynamic therapy of subfoveal choroidal neovascularisation in age-related macular degeneration with verteporfin: one-year results of 2 randomized clinical trials – TAP Report 1: Arch Ophthalmol 1999; 117: 1329–45. MEDLINE
Verteporfin in Photodynamic Therapy Report 2: Verteporfin therapy of subfoveal choroidal neovascularisation in age-related macular degeneration: two year results of a randomized clinical trial including lesions with occult with no classic choroidal neovascularisation. An J Ophthalmol 2001; 131: 541–60.
Wickens J, Blinder KJ: A preliminary benefit-risk assessment of verteporfin in age-related macular degeneration. Drug Saf 2006; 29: 189–99. MEDLINE
Adamis AP, Shima DT, Tolentino MJ et al.: Inhibition of vascular endothelial growth factor prevents retinal ischemia-associated iris neovascularization in a nonhuman primate. Arch Ophthalmol 1996; 114: 66–71. MEDLINE
Aiello LP, Northrup JM, Keyt BA, Takagi H, Iwamoto MA: Hypoxic regulation of vascular endothelial growth factor in retinal cells. Arch Ophthalmol 1995; 113: 1538–44. MEDLINE
Gonzales CR: Enhanced efficacy associated with early treatment of neovascular age-related macular degeneration with pegaptanib sodium: an exploratory analysis. Retina 2005; 25: 815–27. MEDLINE
Gragoudas ES, Adamis AP, Cunningham ET Jr., Feinsod M, Guyer DR: Pegaptanib for neovascular age-related macular degeneration. N Engl J Med 2004; 351: 2805–16. MEDLINE
Calvo-González C, Reche-Frutos J, Donate-López J et al.: Combined Pegaptanib sodium (Macugen) and photodynamic therapy in predominantly classic juxtafoveal choroidal neovascularisation in age related macular degeneration. Br J Ophthalmol 2008; 92: 74–5. MEDLINE
Fung AE, Lalwani GA, Rosenfeld PJ et al.: An optical coherence tomography-guided, variable dosing regimen with intravitreal ranibizumab (Lucentis) for neovascular age-related macular degeneration. Am J Ophthalmol 143: 566–83. MEDLINE
Spaide R: Ranibizumab according to need: a treatment for age-related macular degeneration. Am J Ophthalmol 2007; 143: 679–80. MEDLINE
Chen Y, Wiesmann C, Fuh G et al.: Selection and analysis of an optimized anti-VEGF antibody: crystal structure of an affinity-matured Fab in complex with antigen. J Mol Biol 1999; 293: 865–81. MEDLINE
Shahar J, Avery RL, Heilweil G et al.: Electrophysiologic and retinal penetration studies following intravitreal injection of bevacizumab (Avastin). Retina 2006; 26: 262–9. MEDLINE
Chen CY, Wong TY, Heriot WJ: Intravitreal bevacizumab (Avastin) for neovascular age-related macular degeneration: a short-term study. Am J Ophthalmol 2007; 143: 510–2. MEDLINE
Aisenbrey S, Ziemssen F, Volker M et al.: Intravitreal bevacizumab (Avastin) for occult choroidal neovascularization in age-related macular degeneration. Graefes Arch Clin Exp Ophthalmol 2007; 245: 941–8. MEDLINE
Jonas JB, Libondi T, Ihloff AK et al.: Visual acuity change after intravitreal bevacizumab for exudative age-related macular degeneration in relation to subfoveal membrane type. Acta Ophthalmol Scand 2007; 85: 563–5. MEDLINE
Liew G, Mitchell P: Ranibizumab for neovascular age-related macular degeneration. N Engl J Med 2007; 356: 747–8; author reply 749–50. MEDLINE
Mennel S, Callizo J, Schmidt JC, Meyer CH: Acute retinal pigment epithelial tear in the untreated fellow eye following repeated bevacizumab (Avastin) injections. Acta Ophthalmol Scand 2007; 85: 689–91. MEDLINE
Comparison of Age-Related Macular Generation Treatment Trial (CATT): http://www.med.upenn.edu/cpob/studies/CATT.shtml
Raftery J, Clegg A, Jones J, Tan SC, Lotery A: Ranibizumab (Lucentis) versus bevacizumab (Avastin): modelling cost effectiveness. Br J Ophthalmol 2007; 91: 1244–6 .
Chaudhary V, Mao A, Hooper PL, Sheidow TG: Triamcinolone acetonide as adjunctive treatment to verteporfin in neovascular age-related macular degeneration: a prospective randomized trial. Ophthalmology 2007; 114: 2183–9.
Liggett PE, Colina J, Chaudhry NA, Tom D, Haffner G: Triple therapy of intravitreal triamcinolone, photodynamic therapy, and pegaptanib sodium for choroidal neovascularization. Am J Ophthalmol 2006; 142: 1072–4.
Augustin AJ, Puls S, Offermann I: Triple therapy for choroidal neovascularization due to age-related macular degeneration: verteporfin PDT, bevacizumab, and dexamethasone. Retina 2007; 27: 133–40.
Aisenbrey S, Lafaut BA, Szurman P et al.: Macular translocation with 360 degrees retinotomy for exudative age-related macular degeneration. Arch Ophthalmol. 2002; 120: 451–9.
Joussen AM, Heussen FM, Joeres S et al.: Autologous translocation of the choroid and retinal pigment epithelium in age-related macular degeneration. Am J Ophthalmol 2006; 142: 17–30.
Treatment of age-related macular degeneration with photodynamic therapy (TAP) Study Group Photodynamic therapy of subfoveal choroidal neovascularization in age-related macular degeneration with verteporfin: one-year results of 2 randomized clinical trials—TAP report. Arch Ophthalmol 1999;117(10): 1329–45.
Chakravarthy U, Adamis AP, Cunningham ET Jr et al.: Clinical Trial Group:VEGF Inhibition Study in Ocular Neovascularization (V.I.S.I.O.N.). Year 2 efficacy results of 2 randomized controlled clinical trials of pegaptanib for neovascular age-related macular degeneration. Ophthalmology 2006; 113: 1508. e1–e25. Epub 2006; Jul 7. MEDLINE
D'Amico DJ, Goldberg MF, Hudson H et al.: Anecortave Acetate Clinical Study Group: Anecortave acetate as monotherapy for the treatment of subfoveal lesions in patients with exudative age-related macular degeneration (AMD): interim (month 6) analysis of clinical efficacy and safety. Retina 2003; 23: 14–23.
Slakter JS: Anecortave acetate as monotherapy for treatment of subfoveal neovascularization in age-related macular degeneration: twelve-month clinical outcomes. Ophthalmology 2003; 110: 2372–83.
Slakter JS, Bochow TW, D'Amico DJ et al.: Anecortave Acetate Clinical Study Group: Anecortave acetate (15 milligrams) versus photodynamic therapy for treatment of subfoveal neovascularization in age-related macular degeneration. Ophthalmology 2006; 113: 3–13. MEDLINE
Klais CM, Eandi CM, Ober MD et al.: Anecortave acetate treatment for retinal angiomatous proliferation: a pilot study. Retina 2006; 26: 773–9. MEDLINE
Klais CM, Eandi CM, Ober MD et al.: Anecortave acetate for the treatment of idiopathic perifoveal telangiectasia: a pilot study. Retina 2006: 26: 780–5. MEDLINE
Kuppermann BD, Blumenkranz MS, Haller JA et al.: Dexamethasone DDS Phase II Study Group. Randomized controlled study of an intravitreous dexamethasone drug delivery system in patients with persistent macular edema. Arch Ophthalmol 2007; 125: 309–17. MEDLINE
Nguyen QD, Shah SM, Hafiz G et al.: CLEAR-AMD 1 Study Group: a Phase I trial of an IV-administered vascular endothelial growth factor trap for treatment in patients with choroidal neovascularization due to age-related macular degeneration. Ophthalmology 2006; 113: 1522 e1–e14. MEDLINE
Shen J, Samul R, Silva RL et al.: Suppression of ocular neovascularization with siRNA targeting VEGF receptor 1. Gene Ther 2006; 13: 225–34. MEDLINE
Campochiaro PA, Nguyen QD, Shah SM et al.: Adenoviral vector-delivered pigment epithelium-derived factor for neovascular age-related macular degeneration: results of a Phase I clinical trial. Hum Gene Ther 2006; 17: 167–76. MEDLINE
Brafman A, Mett I, Shafir M et al.: Inhibition of oxygen-induced retinopathy in RTP801-deficient mice. Invest Ophthalmol Vis Sci 2004; 45: 3796–805. MEDLINE
Lima e Silva R, Kachi S, Akiyama H et al.: Transscleral delivery of polyamine analogs for ocular neovascularization. Exp Eye Res 2006; 83: 1260–7. MEDLINE
Lima e Silva R, Saishin Y, Saishin Y et al.: Suppression and regression of choroidal neovascularization by polyamine analogues. Invest Ophthalmol Vis Sci 2005; 46: 3323–30. MEDLINE

 Date HTM PDF 
7 / 2015 0 1
6 / 2015 4 1
5 / 2015 1 0
4 / 2015 4 1
3 / 2015 3 0
2 / 2015 9 2
2015 23 5
2014 70 25
2013 79 22
2012 22 28
2011 57 45
2010 144 32
2009 265 63
Total 660 220

Letters to the Editor

All Letters