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Evaluate the efficacy of pegaptanib, a selective anti-vascular endothelial growth factor (VEGF) agent, and bevacizumab, a nonselective anti-VEGF agent, for retinal pigment epithelial detachment (PED) associated with occult choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD).
Prospective, comparative, nonrandomized pilot study included patients with PED comprising >50% of total lesion in subfoveal location with visual acuity (VA) 20/40–20/400 and lesions either previously untreated or treated only with photodynamic therapy/verteporfin. Seven patients received pegaptanib 0.3 mg intravitreally (IVT); eight received IVT bevacizumab 1.25 mg. Follow-up occurred every 4–6 weeks for 6 months. Reinjection of initial medication occurred if there was intra- or subretinal fluid observed by optical coherence tomography (OCT) or increased PED. Endpoints were mean changes from baseline to month 6 in VA (ETDRS) and foveal thickness.
At baseline, mean VA was lower, and mean foveal thickness was greater in pegaptanib versus bevacizumab-treated patients (36.1 vs 49.5 letters; 470.4 vs 321.1 μm). Mean improvements to month 6 in VA and foveal thickness were greater for pegaptanib (VA: +9.1 vs +7.2 letters; foveal thickness: −88.2 vs −52.9 μm). On average, pegaptanib-treated patients had slower but more sustained improvement in VA and foveal thickness; bevacizumab-treated patients showed rapid improvement with a slow return towards baseline. Both agents were well tolerated.
Intravitreal injections of pegaptanib or bevacizumab are both efficacious and safe treatments for PED associated with occult CNV secondary to AMD.
Retinal pigment epithelial detachment (PED), in which the retinal pigment epithelium (RPE) physically separates from the underlying Bruch’s membrane, occurs in association with many diseases of the retina, the most common being age-related macular degeneration (AMD).1 In patients with AMD, PEDs are classified by clinical appearance and angiographic characteristics as confluent drusen, serous, turbid, hemorrhagic, vascular or fibrovascular, and fibrous or organized.2–5 The underlying pathophysiology of PED is complex and not clearly understood. Several contributing mechanisms have been proposed, the most obvious being displacement of the RPE by exudation from choroidal neovascularization (CNV). Because CNV is not always identified in patients with PED, however, controversy exists as to whether CNV develops as a complication of existing PED6 or whether the growth of CNV vessels through Bruch’s membrane directly causes PED.5 Bird and Marshall7 suggested that PED results when Bruch’s membrane is thickened from the progressive accumulation of lipid or lipoprotein deposits, leading to increased hydrophobic resistance to the normal active transport of fluid and resulting in fluid accumulation beneath the RPE. These hypotheses concerning the pathogenesis of PED are believed not to be mutually exclusive.8
The visual prognosis for patients with CNV-associated PED may be especially poor. In a study that followed 55 eyes of 53 patients for an average of 2.2 years, 62% of patients were reported to have lost 6 or more lines of vision, with 75% having a final visual acuity of 20/200 or worse.9 Elman et al10 reported in a retrospective analysis of the natural history of PED in patients without CNV that 52% of patients maintained an initial visual acuity of 20/20–20/40 through an average of 32.8 months.10 Another study involving 101 eyes reported a similar course of vision loss irrespective of PED type.11 Although patients without CNV may have a better prognosis at the onset, they are at high risk of developing CNV and subsequent vision loss. In the Elman et al study,10 32% of patients eventually developed CNV while in another series,12 67% of patients with serous PED developed CNV after a maximum of 19 months. Since serous PED may obscure the extent of any existent CNV, it should be noted that proper assessment of patients with sub-RPE fluid is often rendered difficult.1
The management of AMD patients with PED is controversial due to the difficulty in determining the presence of associated CNV and the inability to reliably identify those patients with serous PED who are likely to develop CNV and experience severe vision loss. In addition, treatment options for PED are limited and usually of poor outcome. While one trial13 of angiographically directed laser photocoagulation involving 35 eyes reported stabilization or improvement of vision in 60%, other attempts14,15 with both unguided and guided photocoagulation reported much inferior results, with treated eyes faring worse than untreated controls. Results of studies of photodynamic therapy (PDT) with verteporfin have also not been encouraging. Although patients with PED were not specifically studied in either the Treatment of Age-related Macular Degeneration with Photodynamic Therapy (TAP) or Verteporfin in Photodynamic Therapy (VIP) trials,16,17 a recent study18 enrolling lesions of <2 months’ duration found that 60% of patients had improved or stabilized vision over a 16-month follow-up. In contrast, other groups19,20 have reported that PDT with verteporfin conferred little treatment benefit, even when combined with intravitreal triamcinolone acetonide.21 In these trials, treatment was also complicated by subretinal hemorrhage and RPE tears.
Based on the suboptimal treatment outcomes with laser and PDT with verteporfin there is a need for a therapeutic approach that improves the prognosis of PED secondary to AMD. One promising avenue involves agents that inactivate vascular endothelial growth factor (VEGF), the most potent known promoter of angiogenesis22 and vascular permeability23 both of which appear to play a role in the pathogenesis of PED. Two intravitreal VEGF antagonists indicated for the treatment of all angiographic subclasses of CNV are commercially available: pegaptanib, an RNA aptamer, which has high affinity and specificity for the 165 amino acid isoform of VEGF while sparing VEGF121,24,25 and ranibizumab, an Fab antibody fragment that inactivates all VEGF isoforms.26–28 In addition, bevacizumab, an antibody related to ranibizumab, which is indicated for intravenous treatment of cancer in combination with chemotherapeutic agents (see prescribing information at: http://www.gene.com/gene/products/information/oncology/avastin/insert.jsp# indications) and which also inactivates all VEGF isoforms, has been used in off-label studies to treat neovascular AMD.29 The present pilot study examined the effectiveness of pegaptanib and bevacizumab in the treatment of PED associated with occult CNV secondary to AMD. The results are encouraging and merit further study in an appropriately designed randomized clinical trial.
This prospective, comparative, nonrandomized pilot study included patients with PED comprising >50% of the total lesion in the subfoveal location. Eligible patients had visual acuity between 20/40 and 20/400, and lesions that either had not been treated previously or had been treated only with PDT with verteporfin. Visual acuity (Early Treatment Diabetic Retinopathy Study [ETDRS]), a complete ophthalmic examination, indocyanine green angiography, fluorescein angiography, and optical coherence tomography (OCT) were evaluated at baseline. Examinations were completed 5–7 days before the administration of the first intravitreal injection.
The first seven patients presenting with PED received intravitreal injections of commercially available pegaptanib sodium 0.3 mg (Macugen®; [OSI] Eyetech, Inc and Pfizer Inc, New York, USA). The following eight patients received intravitreal injections of bevacizumab 1.25 mg in 0.05 mL prepared in a sterile compounding environment by the pharmacy service of our hospital. Injection procedures were identical for both therapies and included use of povidone iodine 5%, a sterile drape and gloves, and an eyelid speculum. Follow-up visits for each patient occurred every 4 to 6 weeks for 6 months. Each visit included a complete ophthalmic examination, visual acuity assessment (ETDRS), and OCT. Reinjection of the initial medication occurred if there was evidence of intra- or subretinal fluid by OCT or an increase in RPE detachment.
Study endpoints were mean changes from baseline to month 6 in visual acuity (ETDRS and logMAR [logarithm of the minimum angle of resolution]), and in foveal thickness (OCT).
Informed consent was obtained. All applicable institutional and governmental regulations concerning the ethical use of human volunteers were followed during this research.
Characteristics of the 15 patients were similar across treatment groups at baseline (Table 1); two patients who received pegaptanib and three who received bevacizumab had been treated previously with PDT with verteporfin. A mean of 3.7 (range 3–4) and 3.4 (range 2–5) injections of pegaptanib and bevacizumab were administered, respectively.
At baseline, mean visual acuity was lower and foveal thickness was greater in the pegaptanib treated patients (Table 2). Improvements in visual acuity measured by both ETDRS and logMAR and reductions in foveal thickness were seen in each treatment group between baseline and month 6, but functional and anatomical changes were greater for all outcomes among patients treated with pegaptanib. The pattern of improvement varied by treatment (Figure 1). On average, pegaptanib-treated patients had slower but more sustained improvement in visual acuity and foveal thickness while those treated with bevacizumab demonstrated rapid improvement with a diminished effect over time.
Both agents were safe and well tolerated; neither ocular nor systemic complications were observed in any patient.
The principal finding in this pilot study is that both selective VEGF inhibition with pegaptanib and nonselective VEGF inhibition with bevacizumab provided similar anatomical and functional benefits in the treatment of PED, with no safety signals having emerged. These results are similar to those seen in another recent pilot study with bevacizumab, also directed against PED secondary to AMD.30 In the present report the two agents provided qualitatively similar benefits, while pegaptanib-treated patients showed somewhat greater improvements in terms of mean visual acuity and retinal thickness despite the overall poorer baseline condition. The difference in the number of injections administered between the treatment groups was less than 10%, suggesting that undertreatment with bevacizumab was unlikely to be the cause. There also appeared to be a difference in the time courses of the responses to the two drugs, with patients receiving pegaptanib requiring a longer timeframe to achieve visual acuity improvements than bevacizumab, but one that was more sustained over the longer term. It is interesting that for both pegaptanib and bevacizumab the vision seemed to improve despite the fact that the PED size seems to have fluctuated over time.
While the data in the present study must be viewed as preliminary, they suggest that it may not be necessary to inhibit all VEGF isoforms for treatment of PED, in that selective inhibition of VEGF165 with pegaptanib produced comparable effects to bevacizumab. These findings are relevant to safety in that nonselective VEGF inhibition with ranibizumab was found be associated with a significantly higher incidence of nonocular hemorrhage compared to controls.31 In addition, early data from the Safety Assessment of Intravitreal Lucentis for AMD (SAILOR) trial examining ranibizumab safety has indicated a significantly increased risk of stroke for the 0.5 mg versus 0.3 mg dose, prompting a physician advisory letter from the manufacturer which can be found at: http://www.fda.gov/medwatch/safety/2007/Lucentis_DHCP_01-24-2007.pdf. Whether these risks apply to bevacizumab, which is also a nonselective VEGF antagonist, is not known, since its use has not been evaluated in large, properly controlled trials.29
Another issue of concern is the risk of RPE tears, a recognized complication of PED, in patients treated with anti-VEGF therapy. Chang and Sarraf 32 have analyzed reports of RPE tears for all three anti-VEGF agents in the treatment of AMD and found that a pre-existing PED was a common feature. Similar conclusions have been reached in other retrospective studies with bevacizumab.30,33,34 PED is a predisposing factor for RPE tears even in untreated patients, and it remains to be determined whether anti-VEGF therapy accelerates the natural history of these cases, or contributes an additional risk that may require other adjustments in treatment regimens.32
The main limitation of this study is that it enrolled only a small number of patients. Other limitations included a lack of randomization and the relatively short duration of follow-up. Therefore, these findings require confirmation in a larger randomized study, which could also answer questions regarding the optimal dose, long-term efficacy and safety, and criteria for retreatment.
The author reports no conflicts of interest in this work. This paper was supported with a grant from Pfizer Inc.
This study was presented as an oral presentation at the XI Vitreoretinal Spanish Society Congress (“XI Congreso de la Sociedad Española de Retina y Vítreo”), Madrid (16 February 2007).