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Cold Spring Harb Perspect Med. 2012 June; 2(6): a006411.
PMCID: PMC3367538
Copyright © 2012 Cold Spring Harbor Laboratory Press; all rights reserved
Antiangiogenic Therapy for Ischemic Retinopathies
Motasem Al-Latayfeh, Paolo S. Silva, Jennifer K. Sun, and Lloyd Paul Aiello
Beetham Eye Institute, Joslin Diabetes Center, Boston, Massachusetts 02215; and Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts 02215
Correspondence:lpaiello/at/joslin.harvard.edu
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Abstract
Neovascularization is a common pathological process in various retinal vascular disorders including diabetic retinopathy (DR), age-related macular degeneration (AMD) and retinal vein occlusion (RVO). The development of neovascular vessels may lead to complications such as vitreous hemorrhage, fibrovascular tissue formation, and traction retinal detachments. Ultimately, irreversible vision loss may result. Various proangiogenic factors are involved in these complex processes. Different antiangiogenic drugs have been formulated in an attempt treat these vascular disorders. One factor that plays a major role in the development of retinal neovascularization is vascular endothelial growth factor (VEGF). Anti-VEGF agents are currently FDA approved for the treatment of AMD and RVO. They are also extensively used as an off-label treatment for diabetic macular edema (DME), proliferative DR, and neovascular glaucoma. However, at this time, the long-term safety of chronic VEGF inhibition has not been extensively evaluated. A large and rapidly expanding body of research on angiogenesis is being conducted at multiple centers across the globe to determine the exact contributions and interactions among a variety of angiogenic factors in an effort to determine the therapeutic potential of antiangiogenic agent in the treatment of a variety of retinal diseases.
 
The development of neovascularization and vascular leakage is one of the key pathological processes that leads to sight threatening complications in nearly all retinal vascular diseases including diabetic retinopathy (DR) (Sun et al. 2008), age-related macular degeneration (AMD) (Jager et al. 2008), and retinal vein occlusion (RVO) (McIntosh et al. 2010; Rogers et al. 2010). Neovascularization is characterized by the growth of blood vessels that are morphologically and functionally abnormal. Neovascular blood vessels can be highly proliferative but are often structurally deficient and poorly organized as compared with normal, mature vessels. This may result in fragile neovascular fronds that tend to grow on the surface of the retina without the branching pattern characteristic of normal retinal vessels (Henkind and Wise 1974). The development of these neovascular vessels may lead to retinal complications such as vitreous hemorrhage, fibrovascular tissue formation, and traction retinal detachments, often ultimately leading to vision loss (Adamis et al. 1999). The specific structural and functional abnormalities present in neovascular vessels provide targets for the design of novel therapeutic and treatment strategies.
The current standard of care for the majority of ischemic retinal diseases is laser photocoagulation. This treatment approach has been proven effective in large randomized clinical trials at inducing long-term regression of neovascularization; however, such treatment can be associated with potentially vision threatening side-effects and a proportion of patients still continue to develop active neovascularization and consequent visual loss (Chew et al. 2003).
The use of antiangiogenic agents for the treatment of various retinal diseases has recently emerged as a potential adjunct to standard ophthalmic care for ocular neovascularization (Gragoudas et al. 2004; Rosenfeld et al. 2006; Brown et al. 2009; Elman et al. 2010). The majority of antiangiogenic agents with evidence of clinical efficacy at this time generally act by inhibiting vascular endothelial growth factors (VEGF). Anti-VEGF therapies have been shown to be remarkably effective in preventing vision loss from the neovascular and exudative complications of retinal diseases particularly in AMD (Gragoudas et al. 2004; Rosenfeld et al. 2006; Andreoli and Miller 2007; Bashshur et al. 2009) and DR (Elman et al. 2010). They also have the benefit, unlike laser photocoagulation, of not being inherently destructive to the retina and benefits compared with steroids in not causing cataract or elevations in intraocular pressure. Although VEGF plays a major role in these diseases and appears to be an excellent therapeutic target, whether VEGF, another factor, or a combination of factors is the optimal target for antiangiogenic therapy of proliferative retinopathies still remains unanswered. Here, we will discuss the various antiangiogenic therapeutic approaches applicable to the treatment of neovascular retinal disease.
Angiogenic factors have been shown to be central in the pathogenesis of proliferative retinopathies. Of these factors, VEGF has received the most attention in recent years and appears to be responsible for the majority of intraocular angiogenesis of ischemic origin (Aiello et al. 1994; Miller et al. 1994; Pierce et al. 1995). This is especially evident in ischemic retinal diseases such as proliferative diabetic retinopathy, rubeosis iridis, and central retinal vein occlusion (Aiello et al. 1994). Other factors such as angiopoietin, erythropoietin, basic fibroblast growth factor (bFGF), insulin like growth factor (IGF), protein kinase C (PKC) enzymes, TGF, PDGF, and others may have moderating roles. VEGF-A is a heparin-binding homodimeric glycoprotein of 45 kDA (Ferrara and Henzel 1989). The human VEGF-A gene is organized in eight exons, separated by seven introns (Tischer et al. 1991). Alternative exon splicing results in the generation of four different isoforms: VEGF121, VEGF165, which is the most prevalent human form, VEGF189 and VEGF206 (Houck et al. 1991; Tischer et al. 1991). VEGF secretion is dramatically induced by hypoxia (Dor et al. 2001; Semenza 2003) as are other growth factors (epidermal growth factors, TGF, IGF, and PDGF) and some hormones (TSH, ACTH, hCG, and sex hormones) (Ferrara 2004). VEGF is associated with breakdown of blood-retina barrier and increased vascular permeability of the retinal blood vessels (Murata et al. 1995; Mathews et al. 1997).
Angiopoietins are a group of proteins that potentiate the angiogenic effect of other angiogenic cytokines, in particular VEGF. Angiopoietin-1 (Ang-1) promotes vascular network maturation, whereas angiopoietin-2 (Ang-2) initiates neovascularization (Asahara et al. 1998). Both angiopoietins interact with a tyrosine kinase receptor called Tie-2 receptor (Suri et al. 1996; Maisonpierre et al. 1997). The angiopoietin/Tie-2 system has an important role in the pathogenesis of proliferative diabetic retinopathy (Takagi et al. 2003; Cai et al. 2008).
The PKC family is a group of isoenzymes that are involved in intracellular signaling. PKC is involved in some aspects of VEGF expression in diabetic retinopathy although oral therapy does not seem to significantly prevent progression to PDR (Aiello 2002; PKC-DRS Study Group 2005; PKC DRS et al. 2006; PKC-DMES Study Group 2007; Girach et al. 2009).
Erythropoietin stimulates red blood cell formation in response to low-oxygen tension (Jelkmann 1992). It also promotes angiogenic activity in vascular endothelial cells (Carlini et al. 1995; Ribatti et al. 1999). In the eye, erythropoietin is a potent retinal angiogenic factor independent of VEGF and is capable of stimulating ischemia-induced retinal angiogenesis in proliferative diabetic retinopathy (Watanabe et al. 2005). In addition, the plasma kallikrein-bradykinin system has been implicated in the increased retinal vascular permeability mediated by angiotensin and carbonic anhydrase enzymes, also through a VEGF independent mechanism (Gao et al. 2007; Phipps et al. 2009).
There are three main mechanisms by which antiangiogenesis agents are used for the treatment of proliferative retinopathies. These mechanisms include: (1) Inhibition of VEGF through direct binding; (2) Inhibition of VEGF synthesis; and (3) Inhibition of VEGF signaling.
Currently there are four agents that inhibit of VEGF through direct binding that are being evaluated or used for the treatment of proliferative retinal diseases: Pegaptanib, Bevacizumab, Ranibizumab, and VEGF Trap. Pegaptanib is a pegylated ribonucleic acid aptamer that specifically binds human VEGF165 with high affinity (Ruckman et al. 1998). Bevacizumab is a humanized form of the murine anti-VEGF-A antibody. It can block all forms of VEGF-A. It was originally FDA approved for treatment of metastatic colon cancer, and has since been approved for chemotherapeutic use in multiple other cancers (Ferrara et al. 2005). It is not FDA approved for any ocular indication. Ranibizumab is an optimized Fab fragment of the anti-VEGF-A antibody bevacizumab. It binds and inhibits all isoforms of VEGF-A (Rosenfeld et al. 2005). It has FDA approval for intraocular use for treatment of neovascular AMD and macular edema secondary to retinal vein occlusion. VEGF trap is a novel fusion decoy protein that is specifically designed to bind all forms VEGF and PDGF with a very high affinity. It is constructed by fusing specific domains from VEGF Receptors 1 and 2 with Fab fragment of IgG resulting in an extremely high affinity for VEGF (kD of ≈1–10 pM for VEGF121) (Holash et al. 2002).
An approach to inhibition of VEGF synthesis has involved the use of small-interfering RNA (siRNA) sequences that silence specific genes that have homology with the injected siRNA sequences. The delivery of siRNA sequences directed against the VEGF gene can potentially inhibit both synthesis and secretion of intracellular VEGF by blocking VEGF gene expression (Kaiser 2006).
Certain tyrosine kinase receptor inhibitors and peroxisome proliferators-activated receptor-γ (PPAR-γ) agonists can inhibit VEGF signaling. VEGF exerts its action by stimulating high-affinity receptors on endothelial cells. The signaling mechanism involves tyrosine residue phosphorylation of the receptors (Aiello et al. 1995). Inhibiting tyrosine kinase activity can result in significant suppression of the neovascular activity of VEGF (Aiello et al. 1997). PPAR γ agonists angiogenesis in animal models by indirectly affecting the function of VEGF (Panigrahy et al. 2002). PPAR-γ agonists such as rosiglitazone and pioglitazone have been used clinically to decrease insulin resistance and improve glycemic control (Aljada et al. 2008). Interestingly, use of Rosiglitazone may delay the onset of proliferative retinopathy in type 2 diabetes because of its antiangiogenic properties (Fig. 1) (Shen et al. 2008).
Figure 1.
Figure 1.
Effect of rosiglitazone on the onset of proliferative diabetic retinopathy patients with severe nonproliferative diabetic retinopathy (NPDR) at baseline. Kaplan-Meier survival curve showing cumulative percentage progression to proliferative diabetic retinopathy (more ...)
Age-Related Macular Degeneration
AMD is the leading cause of blindness in the population over 65 years of age in USA, Europe, and Australia (Congdon et al. 2004). There are two main types of AMD: nonneovascular and neovascular. Nonneovascular AMD is characterized by the presence of hard or soft drusen and retinal pigment epithelial (RPE) changes. Geographic atrophy of the RPE is present in advanced nonneovascular AMD (Bressler et al. 1988). In contrast, neovascular AMD is characterized by the presence of choroidal neovascular membranes (CNVM) that are often associated with subretinal fluid, hemorrhage, and eventually subretinal fibrosis and loss of vision (Votruba and Gregor 2001). Key risk factors for AMD include advanced age and positive family history of AMD, race, smoking, and hypertension (Age-Related Eye Disease Study Research Group 2000; Klein et al. 2004; Clemons et al. 2005).
Angiogenesis in AMD
The pathology in AMD is a result of a combination of multiple mechanisms, some of which are not as yet completely understood. Oxidative stress is believed to be an important contributing factor to the development of AMD (Beatty et al. 2000; Age-Related Eye Disease Study Research Group 2001). Age-related inflammatory processes have also been implicated. Genetic variations in the factor H gene are highly associated with an increased risk of AMD (Edwards et al. 2005). Factor H is a major inhibitory factor for the complement system and gene mutations may led to sustained activation of the complement system that resulting in photoreceptor and RPE atrophy, and Bruch’s membrane disruption with resultant choroidal neovascularization (Donoso et al. 2006).
The development of CNVM presumably results from an increase in angiogenic stimuli that overcome compensatory antiangiogenic mechanisms in the eye. This imbalance may be the result of tissue hypoxia, inflammation or a combination of both. VEGF is found in high concentrations in the CNVM of patients with AMD, while in contrast, pigment-epithelium derived factor (PEDF), a photoreceptor neurotrophic factor with antiangiogenic properties, is found to have lower concentrations in the vitreous with advancing age (Nowak 2006).
Therapies for AMD: Role of Antiangiogenic Drugs
Identifying an effective treatment approach to limit visual complications and improve visual outcomes in neovascular AMD has been the subject of much research. Laser photocoagulation of CNVM was used initially in an attempt to preserve vision. Laser treatment reduced the rate of severe visual loss (loss of six lines or more), preserved patient reading speed and maintained stable contrast sensitivity (Macular Photocoagulation Study Group 1993). However, this treatment modality is not appropriate for patients with subfoveal lesions, and is associated with a high recurrence rate of up to 51% (Macular Photocoagulation Study Group 1991).
Photodynamic therapy (PDT), which uses the combination of photosensitizing agents and low energy laser to achieve selective destruction of CNVM (Miller et al. 1999), is another treatment option. PDT was the first treatment approach found to be effective by large randomized clinical trials for subfoveal lesions. Two major clinical trials, Treatment of Age-related Macular Degeneration With Photodynamic Therapy (TAP) and Verteporfin In Photodynamic therapy (VIP), showed that fewer patients in the PDT group lost 15 letters of vision as compared with the placebo group (37%–54% vs. 62%–67%, duration of follow-up = 24 months) (Bressler 2001; Verteporfin in Photodynamic Therapy Study Group 2001). However, patients with good initial visual acuity or larger subfoveal lesions had a less favorable outcome (Bressler 2001; Verteporfin in Photodynamic Therapy Study Group 2001). Despite the initial success in preventing immediate blindness, the rate of vision improvement remained low, with only 13%–16% of patients gaining one line or more of vision (Bressler 2001; Verteporfin in Photodynamic Therapy Study Group 2001).
A dramatic advancement in the treatment of neovascular AMD was attained with the introduction of antiangiogenic drugs. Multiple large randomized trials established the efficacy of treatment with anti-VEGF agents not only to reduce the incidence of vision loss, but also improve vision in more than 30% of patients (Gragoudas et al. 2004; Rosenfeld et al. 2006; Brown et al. 2009).
Gragoudas et al. showed that pegaptanib reduced the incidence of moderate and severe visual loss in the treatment groups. The percentage of patients who lost less than 15 letters increased from 55% in the control group to 70% in the treatment groups. In addition, the incidence of severe vision loss dropped from 22% in the control group to 10% in the treatment groups. Mean visual acuity was significantly better in the treatment groups as compared with the control group (Gragoudas et al. 2004).
Two of the largest trials in AMD, the MARINA (Minimally Classic/Occult Trial of the Anti-VEGF Antibody Ranibizumab in the Treatment of Neovascular Age-Related Macular Degeneration) and ANCHOR (Anti-VEGF Antibody for the Treatment of Predominantly Classic Choroidal Neovascularization in Age-Related Macular Degeneration) trials, established the efficacy of ranibizumab compared to sham injection and PDT in preventing visual loss in patients with CNVM (Rosenfeld et al. 2006; Brown et al. 2009). The MARINA trial is a phase III trial that compared two doses of ranibizumab (0.3 mg or 0.5 mg) to sham injections in patients with occult or minimally classic CNVM. It showed that the percentage of patients that lost less than three lines of vision in both ranibizumab groups was 95% compared to 62% in the sham group after 1 year. Also, about one third of patients in the ranibizumab groups gained more than three lines of vision compared to 2% in the control group (Rosenfeld et al. 2006). The ANCHOR trial compared repeated intravitreal injections of two doses of ranibizumab (0.3 mg and 0.5 mg) to PDT in patients with predominantly classic CNVM. The results showed that the percentage of patients who lost fewer than 15 letters was 90% and 90% for the 0.3 mg and 0.5 mg ranibizumab groups, respectively, as compared with 66% of those in the verteporfin group. Visual acuity improved by 15 letters or more in 34% of the 0.3-mg group and 41% of the 0.5-mg group, as compared with 6% of the verteporfin group (Brown et al. 2009). The PIER study is another phase III study that attempted to compare two doses of ranibizumab (0.3 mg and 0.5 mg) given monthly for the first three months then quarterly for 12 months, with sham injection. The 12-month results showed that treatment with ranibizumab resulted in significantly less vision loss compared to sham group (mean letter change in both ranibizumab groups was -1.6 and -0.2 letters compared to -16.3 in the sham group, p < 0.0001). In addition, the percentage of patients who lost less than 15 letters was 83% and 90% for the 0.3 mg and 0.5 mg ranibizumab groups respectively, compared to 49% in the sham group (Regillo et al. 2008). The 24-month results showed that the visual benefits in the first 12 months of the study were maintained through the second year. However, both ranibizumab groups were switched to a monthly regimen after month 19. The PIER report concluded that the visual outcome of the quarterly regimen is not as robust as the monthly regimen followed in the MARINA and the ANCHOR studies (Abraham et al. 2010).
All the above mentioned studies, as well as others, have reported a good safety profile for intravitreal ranibizumab in AMD. The per-injection rate of endophthalmitis has been less than 0.1% in all studies. One phase IIIb study has found a nonstatistically significant difference toward a higher rate of cerebrovascular stroke in the 0.5 mg ranibizumab group versus the control group, but no such trend was observed for myocardial infarction or arterial thrombotic events overall (Boyer et al. 2009).
Intravitreal bevacizumab was initially reported to be effective in AMD in several small clinical trials of relatively short duration (Bashshur et al. 2009; Rosenfeld et al. 2005a). More recent results from a large phase III, multicenter randomized controlled trial, the Comparison of Age-related Macular Degeneration Treatments Trials (CATT), have showed that bevacizumab, when used for treatment of neovascular AMD by the same protocol as ranibizumab (either dosed monthly or on a prn basis), is noninferior to the use of ranibizumab (CATT research Group et al. 2011). Rates of thromboembolic events, including death, myocardial infarction, and stroke, were also similar between patients who received bevacizumab as compared with ranibizumab. The proportion of patients with serious systemic adverse events was higher in the bevacizumab treated group, but these events were not related to complications that had previously been identified as relating to anti-VEGF therapy.
Other agents are also being investigated for treatment of AMD. Initial trials on VEGF trap showed that it appears effective and well tolerated in AMD patients (Nguyen et al. 2009). Phase II trials have also shown improvements in vision and reductions in retinal thickness with the use of VEGF trap as treatment for neovascular AMD over up to a 1-year period (Brown et al. 2011; Heier et al. 2011). Phase III trials (VIEW1 and VIEW2) are now underway to establish the clinical efficacy of VEGF trap compared to ranibizumab. Also, bevasiranib, which is a siRNA molecule known previously as Cand5, showed some efficacy in reducing the rate of vision loss in AMD when combined with ranibizumab (Singerman 2009). Another group of drugs that are currently being evaluated for AMD are tyrosine kinase receptor blocking agents for which animal studies have shown that some topical agents result in up to 58% reduction of the size of the CNVM in rats with no apparent ocular or systemic toxicity (Takahashi et al. 2009). Clinical trials are ongoing. Results are expected within the next few years and could potentially further improve the visual outcomes in patients with neovascular AMD.
CNVM is a pathologic feature in various diseases other than AMD such as pathologic myopia, angioid streaks, ocular histoplasmosis, and traumatic choroidal rupture. In a controlled clinical trial that compared bevacizumab with PDT in myopic CNV, 49% of the bevacizumab treatment group gained two lines or more of vision after single injection with a sustained effect over 1 year. The mean best-corrected visual acuity (BCVA) improved more in the bevacizumab group compared to the PDT or control groups. In addition, treatment with bevacizumab resulted in more regression of CNVM and less chorioretinal atrophic changes compared to the PDT group (Hayashi et al 2009). Multiple studies have reported on the benefit of bevacizumab in myopic CNVM, which can lead to more than 15 letters gain of visual acuity in 40% to 75% of patients. Those findings have led toward wider use of anti-VEGF agent in these disorders (Ikuno et al. 2009; Gharbiya et al. 2010). Other studies have shown potential benefit of bevacizumab in treatment of CNVM related to angioid streaks and ocular inflammatory diseases (Mansour et al. 2009; Wiegand et al. 2009).
Diabetic retinopathy is the leading cause of visual loss in the working age group in the United States and other developed countries (Klein et al. 1984). Visual loss from diabetic retinopathy is primarily caused by complications arising from neovascularization in proliferative retinopathy (PDR) or exudation and retinal thickening associated with the development of diabetic macular edema (DME) (Fong et al. 1999).
Laser photocoagulation had remained the standard care for both of these complications for the past 25 years (Ferris et al. 1999). Although there remains a clear role for laser in the treatment of these disorders, recent studies have shown that antiangiogenic approaches combined with either prompt laser or deferred laser result in better visual outcomes for patients with diabetic macular edema than laser alone (Aiello et al. 1994). Long term outcomes of anti-VEGF therapy for the treatment of diabetic macular edema are still being evaluated; however, visual improvement rates are nearly double, and visual loss rates only one third of those with laser alone (Fig. 2). This marked benefit is making anti-VEGF therapy the current primary interventional approach for patients with center involved diabetic macular edema and reduced vision.
Figure 2.
Figure 2.
Effect of anti-VEGF therapy on vision and retinal thickening. The DRCR.net has published the 1-year results of a phase III trial that evaluated the safety and efficacy of intravitreal 0.5-mg ranibizumab or 4-mg triamcinolone treatments combined with focal/grid (more ...)
Metabolic changes in diabetes lead to alterations in the retinal vasculature eventually resulting in reduced perfusion of the retinal tissue and retinal ischemia (Stefansson 2006). This ischemia induces the activity of hypoxia-induced factor (HIF) which up-regulates VEGF expression and the transcription of various other angiogenic factors (Ozaki et al. 1999). In addition to the ischemic stimulus, VEGF expression is also increased by inflammatory mediators (Rojas et al. 2010). The role of VEGF in PDR is supported by studies that reported high concentrations of VEGF in the vitreous of patients with PDR and its excellent correlation with disease activity (Aiello et al. 1994; Adamis et al. 1999). Patients with quiescent PDR had low or undetectable VEGF concentrations and VEGF concentrations were low after successful laser treatment (Aiello et al. 1994). A direct role for VEGF mediation of the neovascular response in PDR was indicated by the fact that vitreous fluids from patients with active PDR were angiogenic in vitro, and this angiogenic stimulus could be blocked using a VEGF specific inhibitor.
Despite the excellent responses to anti-VEGF agents observed with certain diseases thus far, there are a substantial percentage of individuals who do not appear to respond robustly to these therapies. This fact, as well as the complex mechanisms regulating in vivo angiogenesis, strongly suggests that there may important factors other than VEGF involved in mediating these conditions. Erythropoietin (EPO) is a potent angiogenic mediator that is thought to act independently of VEGF. Watanabe et al. showed that erythropoietin is present in high concentrations in the vitreous of patients with PDR compared to controls. This study provided the first evidence that EPO acts on the angiogenic pathway independently from VEGF and is more strongly correlated with the presence of PDR than VEGF (Watanabe et al. 2005). Subsequent studies have shown genetic mutations can increase EPO expression and this is associated with increased risk of PDR and related condition in patients and in animals (Tong et al. 2008; Chen et al. 2009; Xiong et al. 2009; Abhary et al. 2010).
Other angiogenic factors are the angiopoietin/Tie-2 system which, as mentioned earlier, modulates the effect of VEGF on endothelial cells (Takagi et al. 2003; Cai et al. 2008). Several cytokines also have been shown to have a role in new vessel formation in PDR such as insulin-like growth factor-1 (IGF-1), interleukin-8, placental growth factor, hepatocyte growth factor, platelet-derived growth factor (PDGF), and leptin (Simo et al. 2006). In addition, hyperglycemia results in loss of PDGF survival action thus leading to pericyte apoptosis and diabetic vasculopathy. The probable mechanism involves hyperglycemia-induced activation of protein kinase C-δ (PKC-δ) which leads to increased expression of a protein tyrosine phosphatase called Src homology-2 domain–containing phosphatase-1 (SHP-1). In addition to possibly mediating hyperglycemic memory, this pathway may be important in early onset of retinopathy via loss of retinal pericytes and increase susceptibility of endothelial cells to damage and subsequent hypoxia (Geraldes et al. 2009).
Antiangiogenic factors have also been documented to be present in the eye at various stages of retinopathy (Praidou et al. 2010). Pigment epithelium derived factor (PEDF) has antiangiogenic properties in vitro and is present in the eye. PEDF concentration was found to be lower in patients with diabetes, and in patients with active PDR compared to other retinopathies (Ogata et al. 2001). Animal studies have showed that PEDF down-regulates VEGF and interferes with VEGF-receptor interaction in diabetic retinopathy (Zhang et al. 2006).
Panretinal laser photocoagulation remains the standard treatment for PDR. With timely and appropriate application, more than 95% of the associated severe visual loss can be prevented. However, it is now clear that inactivation of the angiogenic stimulus can at least temporarily induce regression of retinal neovascularization (Fig. 3). Methods for pharmacologically inducing long-term regression of PDR are being studied. Different anti-VEGF agents have shown potential benefit in PDR. Mendrinos et al. (2009) published a case report demonstrating rapid regression of neovascularization after a single injection of pegaptanib, which was sustained for more than 15 months.
Figure 3.
Figure 3.
Figure 3.
Effect of anti-VEGF agents on retinal neovascularization and macular edema. (A) An intravitreal injection of the anti-VEGF agent bevacizumab has been shown to induce a marked regression of retinal neovascularization beginning as early as 1 day after injection (more ...)
Bevacizumab has been shown by Avery et al. (2006) to induce regression of new vessels in PDR as early as 24 hours after injection but with a variable sustained effect ranging between 2 to 11 weeks. Jorge et al. (2006) showed a short-term resolution of leakage from retinal neovascularization at 6 weeks after a single intravitreal injection of bevacizumab in 15 patients with persistent new vessels despite panretinal laser photocoagulation. At 12 weeks, 14 out of 15 patients showed recurrent leakage but to a lesser extent than at baseline (Jorge et al. 2006). Similar studies have reported similar short term efficacy of bevacizumab in inducing regression of retinal neovascularization (Mirshahi et al. 2008; Tonello et al. 2008; Erdol et al. 2010). Currently, the Diabetic Retinopathy Clinical Research Network (DRCR.net) is conducting two trials: one to study the efficacy of ranibizumab in cases of vitreous hemorrhage caused by PDR, and another to assess the efficacy of adjunctive use of ranibizumab compared to triamcinolone with laser treatment in PDR. The results of these trials will help further define the role of anti-VEGF treatment in the management of diabetic ocular neovascular complications.
Bevacizumab has shown some benefit as an adjunctive therapy prior to vitrectomy in patients with PDR. Small prospective and retrospective uncontrolled studies have suggested that preoperative bevacizumab facilitates vitrectomy by decreasing intra-operative bleeding and postoperative vitreous hemorrhage, resulting to better visual outcomes (Ahmadieh et al. 2009; Modarres et al. 2009; Oshima et al. 2009; Hernandez-Da Mota and Nunez-Solorio 2010). However, cases of rapid contraction and regression of fibrovascular membranes associated with preoperative intravitreal anti-VEGF agents have been reported to cause progressive tractional detachment particularly in patients who had no previous laser therapy or had a severe ring-like fibrosis threatening the macula (Oshima et al. 2009).
Bevacizumab has been shown to be effective in the management of iris neovascularization (NVI) and neovascular glaucoma (NVG). Wakabayashi et al. (2008) published a retrospective analysis of 41 eyes with NVI and NVG treated with intravitreal bevacizumab with mean follow-up of 13.3 months (range 6–22 months). The cohort included patients with NVI alone, open-angle NVG (O-NVG) and closed-angle NVG (C-NVG). One week after the first intravitreal bevacizumab injection NVI regressed in all NVI alone patients. However, 44% of patients experienced recurrence of the NVI, which again regressed after subsequent repeat injections and laser treatment. For patients with O-NVG, 71% showed initial normalization of IOP. However, 58% of the neovascularization recurred within the first 6 months, and 29% of patients required surgery during the follow-up period. For the C-NVG, intravitreal bevacizumab failed to normalize the IOP in nearly all of the patients and 93% required surgery to control the IOP during the first 2 months of intravitreal bevacizumab treatment despite initial regression of new vessels. The investigators concluded that intravitreal bevacizumab may be effective in the initial stages of iris neovascularization, and it may be a good adjunct for surgical treatment of advanced cases since it may reduce bleeding from the new vessels and potentially may improve surgical outcomes (Wakabayashi et al. 2008). Several other studies showed similar short-term benefits of intravitreal bevacizumab in the management of NVG and NVI (Avery 2006; Davidorf et al. 2006; Brouzas et al. 2009).
Overall, anti-VEGF agents appear very effective in inducing rapid initial regression of ischemia induced ocular neovascularization, but the effect is temporary and requires either additional definitive treatment (such as laser photocoagulation) or development of continuous delivery mechanisms, molecules with longer duration of action or repeated intraocular administration. Large multicenter controlled clinical trials are required to establish the long-term efficacy and determine the best use of anti-VEGF agents in the management of PDR and neovascular glaucoma. Furthermore, the safety of continuous or long-term repeated exposure of retinal and choroidal tissue to VEGF inhibition is yet to be established.
Diabetic macular edema is the leading cause of moderate visual loss among patients with diabetes and can occur at any stage of retinopathy. It results from the accumulation of extracellular fluid within the retinal tissue caused by breakdown of retina-blood barrier and if left untreated ultimately will lead to visual loss. Chronic hyperglycemia leads to alternations in different cellular and molecular pathways leading to the breakdown of endothelial barrier and leakage of intravascular fluids into the extracellular space. Several mechanisms have been proposed to explain the pathogenesis of macular edema including hypoxia, inflammatory mediators, renin-angiotensin system, kallikrein-bradykinin system, protein kinase C (PKC), (Xia et al. 1996; Aiello 2002) and VEGF (Aiello et al. 1997; Ruckman et al. 1998). Several investigators found that VEGF, in particular VEGF-A165, is a key factor in increasing vascular permeability. VEGF was found to induce structural changes in the endothelial tight junctions leading to increased permeability (Antonetti et al. 1999).
The repeated intravitreal administration of anti-VEGF agents have been shown to be more effective than conventional focal/grid laser alone in the treatment of diabetic macular edema (Elman et al. 2010). The Macugen Diabetic Retinopathy Study group recently presented data for the phase III trial for the treatment of DME with pegaptanib (Macugen®). In this study, 260 patients with DME were randomized to 0.3 mg pegaptanib or a sham injection every 6 weeks for the first year. In the second year, further injection was determined by the investigator based on the specific criteria. Laser treatment can be given starting from week 18 if deemed necessary by the investigator. The primary endpoint was the proportion of patients who experienced an improvement in vision from baseline of two lines, or 10 letters, on the ETDRS eye chart at 1 year. At 1 year, 37% of pegaptanib patients experience an improvement of 10 letters or more, compared to 20% of sham-treated patients (p = 0.0047). On average, pegaptanib patients gained 5.2 letters of vision at year 1 compared to 1.2 letters for patients receiving sham. At the end of year 2, pegaptanib patients had gained on average 6.1 letters of vision compared to 1.3 letters for patients in the sham arm of the study (P < 0.01) (Sultan et al. 2011).
The DRCR.net conducted a pilot phase II trial to determine the efficacy and safety of intravitreal bevacizumab in the treatment of DME. The study compared five treatment groups: focal laser treatment alone, two groups with two different doses of bevacizumab (1.25 mg and 2.5 mg) at week 0 and 6, and two additional groups in which 1.25 mg bevacizumab was replaced by sham at week 6 or combined with laser treatment at week 3. The efficacy analysis was performed at 12 weeks and the 24-month safety results were reported as well. Compared with the focal laser-alone group, the bevacizumab groups showed a greater reduction in retinal thickness at 3 weeks but were not significantly different from the control group after that. Compared to the focal-laser alone group, the bevacizumab groups showed a larger improvement in vision with a median improvement in visual acuity of about 1 line at the 3-week visit, which was sustained through 12 weeks. The results of this pilot study suggested potential benefit of bevacizumab in the treatment DME but definitive efficacy results need a long-term phase III trial (Scott et al. 2007). The READ-2 study (Ranibizumab for Edema of the mAcula in Diabetes) has also reported the phase II results on the efficacy of ranibizumab in DME compared to laser treatment. The study compared three treatment groups: 0.5 mg intravitreal ranibizumab (group 1), focal laser photocoagulation (group 2), and combined ranibizumab with focal laser (group 3). The results showed that the ranibizumab treated patients had better visual outcome over 6 months of follow-up. At month 6, the mean gain in best-corrected visual acuity (BCVA) was significantly greater in group 1 (+7.24 letters, p = 0.01) compared with group 2 (-0.43 letters), and group 3 (+3.80 letters) was not statistically different from groups 1 or 2 (Nguyen et al. 2009).
The DRCR.net has published the 1-year results of a phase III trial comparing focal grid laser alone to ranibizumab with prompt or deferred focal/grid laser, or intravitreal triamcinolone with prompt focal/grid laser (Fig. 2) (Elman et al. 2010). It is the largest and most comprehensive randomized controlled trial to date on ranibizumab for the treatment of diabetic macular edema. The patients were randomized into four treatments arms: 0.5 mg intravitreal ranibizumab with prompt laser treatment (n = 187), 0.5 mg intravitreal ranibizumab with deferred laser treatment (n = 188), focal/grid laser alone with sham injection (n = 293) and 4 mg intravitreal triamcinolone with prompt laser treatment (n = 186). For the 1-year primary outcome, the mean change in the visual acuity letter score from baseline was significantly greater in the ranibizumab with prompt laser group (+9, p = 0.001) and ranibizumab with deferred laser group (+9, p = 0.001) but not in the triamcinolone with prompt laser group (+4, p = 0.31) as compared with sham injections and prompt laser (+3). The results also reflected both a greater proportion of eyes with a substantial improvement of 10 letters or more (50% and 47% vs. 28%) and 15 letters or more (30% and 28% vs. 15%) and a lower proportion of eyes with a substantial worsening of 10 letters or more (4% and 3% vs. 13%) and 15 letters or (2% and 2% vs. 8%) in the 2 ranibizumab groups compared with the sham + prompt laser group. The study reported that preliminary 2-year outcomes generally mirrored the 1-year primary outcome results but the 2-year follow-up has only been completed for 57% of patients. The OCT results comparing the sham/prompt laser and the ranibizumab groups generally paralleled the overall visual acuity results, favoring the ranibizumab groups. The study reported a favorable safety profile for intravitreal ranibizumab with 0.08% incidence of endophthalmitis and no significant increase in the cardiovascular events compared to controls.
An interesting finding that was noticed by subgroup analysis was a beneficial effect on retinopathy progression (Fig. 4). Both ranibizumab groups showed a trend toward a reduction in 2-level retinopathy progression and an increase in 2-level retinopathy regression, but this was not statistically significant. Using a surrogate of retinopathy progression, both the ranibizumab and triamcinolone groups showed statistically significant reduction in the incidence of vitreous hemorrhage and the need for panretinal laser photocoagulation compared to sham-focal/grid laser group (3%, p = 0.002 and 3%, p = 0.02, respectively, vs. 8%) (Elman et al. 2010). Similar effect on retinopathy progression has been seen in other anti-VEGF studies.
Figure 4.
Figure 4.
Among patients with severe NPDR or worse, intravitreal injections of anti-VEGF agents has tended to reduce retinopathy progression and an increase retinopathy regression (Elman et al. 2010). A similar association was also observed in the rates of panretinal (more ...)
The first-year results of another phase III trial that compares ranibizumab to laser treatment (Efficacy and Safety of Ranibizumab in Patients With Visual Impairment Due to Diabetic Macular Edema [RESTORE]) have also been reported. The study included 345 patients that were divided into three treatment groups: ranibizumab with sham laser, laser with sham injection, and combined ranibizumab/laser. The results showed that 37% of patients treated with ranibizumab 0.5 mg alone, and 43% of those treated with ranibizumab plus laser therapy, had substantial vision improvement of 10 letters or more compared to 16% of patients treated with laser alone. The RESTORE study showed that over 1 year, patients treated with ranibizumab plus laser gained 5.9 letters and those treated with ranibizumab gained 6.1 letters whereas, patients receiving laser therapy gained only 0.8 letters compared to baseline (Mitchell et al. 2011).
There are two ongoing phase III trials that are evaluating the efficacy of ranibizumab compared to sham injection (A Study of Ranibizumab Injection in Subjects With Clinically Significant Macular Edema With Center Involvement Secondary to Diabetes Mellitus [RIDE] and A Study of Ranibizumab Injection in Subjects With Clinically Significant Macular Edema With Center Involvement Secondary to Diabetes Mellitus [RISE]). Both studies have enrolled approximately 366 patients and will be completed in 2012.
Other anti-VEGF therapies for macular edema such as VEGF trap have been shown in phase I trials to have encouraging efficacy and good safety profile in DME. The VEGF trap study included five patients given single 4.0 mg of VEGF trap and followed up over 6 weeks. By the end of the follow-up duration, most of the patients showed a trend toward visual acuity improvement and reduction in central foveal thickness (Do et al. 2009).
PKC-β inhibitor, ruboxistaurin, given orally, has been shown to delay progression of DME to a sight-threatening stage and may ameliorate edema-associated visual decline in patients with persisting severe DME (PKC-DMES Study Group 2007; Davis et al. 2009). PKC-DRS2 group conducted a large multicenter randomized study in which they compared 32 mg of ruboxistaurin given orally to placebo over 36 months. The study included 685 patients from approximately 70 centers. Ruboxistaurin reduced the risk of moderate visual loss to 5.5% compared to 9.1% in placebo-treated patients (p = 0.034). In addition, mean visual acuity was better in the ruboxistaurin-treated patients after 12 months (15 letters improvement: 4.9% vs. 2.4%, and 15-letter worsening: 6.7% vs. 9.9% in ruboxistaurin-treated patients relative to placebo, p = 0.005). Ruboxistaurin treatment also was associated with less frequent progression of edema to within 100 µm of the center (68% vs. 50%, p = 0.003). Treatment with ruboxistaurin reduced the risk of initial laser treatment by 26% (p = 0.008) (Aiello et al. 2006). Further clinical studies of ruboxistaurin are ongoing.
Following diabetic retinopathy, retinal vein occlusion (RVO) is the second most common retinal vascular disease that leads to substantial visual loss (Cugati et al. 2006). The ischemic form of RVO is often complicated by macular edema, retinal, and iris neovascularization. RVO is usually classified into central retinal vein occlusion (CRVO) and branch retinal vein occlusion (BRVO) (Hayreh et al. 1994). The main pathophysiologic mechanisms for vision loss in RVO are ischemia or macular edema (The Central Vein Occlusion Study Group 1997). As discussed earlier, ischemia induces the production of various cytokines that will lead to new blood vessels formation and increased capillary permeability. Early studies showed that VEGF is up-regulated in the retinas of patients with RVO (Aiello et al. 1994; Pe’re et al. 1998). VEGF and IL-6 also has been found to have high concentrations in patients with RVO (Noma et al. 2010) and are highly correlated with the severity of macular edema (Boyd et al. 2002; Noma et al. 2010). The Standard Care vs. Corticosteroid for Retinal Vein Occlusion (SCORE) study reported outcomes in both CRVO (1.0 mg or 4.0 mg intravitreal triamcinolone compared with observation) and BRVO (1.0 mg or 4.0 mg intravitreal triamcinolone compared with grid laser). The results of SCORE-CRVO study showed that the visual outcome in patients treated with an intravitreal injection of triamcinolone improved compared to observation alone and that the 1.0 mg triamcinolone dose has a superior safety profile compared to the 4.0 mg dose.
In the SCORE-BRVO study, both intravitreal triamcinolone and laser treatment achieved comparable results; however, the rates of adverse events (intraocular pressure elevation and cataracts) were highest with the 4.0 mg dose. The investigators recommended that laser treatment continue to be a component of the standard of care in the treatment of macular edema in patients with BRVO (Ip et al. 2009; Scott et al. 2009). The treatment of macular edema in CRVO and BRVO with intravitreal ranibizumab is based largely on the results of two multicenter controlled clinical trials: The Ranibizumab for the Treatment of Macular Edema after Central Retinal Vein Occlusion Study (CRUISE) and Ranibizumab for the treatment of macular edema following Branch Retinal Vein Occlusion: Evaluation of Efficacy and Safety (BRAVO) study. A total of 392 patients participated in CRUISE and 397 patients participated in BRAVO and were randomized into three treatment groups: 0.3 mg and 0.5 mg ranibizumab and sham group. Patients were given monthly injection for the first 6 months, followed by monthly observation and as needed injections for additional 6 months (Brown et al. 2010; Campochiaro et al. 2010). The 6 months results for BRAVO showed that the percentage of patients in the ranibizumab 0.5 mg group who gained 15 letters or more in BCVA from baseline was 61%, compared with 29% in the sham group. Patients who received ranibizumab 0.5 mg had a mean gain of 18.3 letters versus 7.3 letters in patients receiving sham injections (Campochiaro et al. 2010). Similarly, in CRUISE, the percentage of patients in the ranibizumab 0.5 mg group who gained 15 letters or more in BCVA from baseline was 48%, compared with 17% in the sham group. Patients who received ranibizumab 0.5 mg had a mean gain of 14.9 letters versus 0.8 letters for patients receiving sham injections (Brown et al. 2010). The 12-month results have been presented recently and show persistent benefits of improved visual outcomes throughout the follow-up period (Brown et al. 2011). Bevacizumab also showed similar efficacy in several small and uncontrolled studies for the treatment of macular edema secondary to RVO (Gregori et al. 2008; Prager et al. 2009; Beutel et al. 2010).
The introduction of pharmacologic treatments targeting antiangiogenic factors has revolutionized the management of proliferative and exudative complications of the most common sight threatening retinopathies. Based on the results of large multicenter randomized controlled clinical trials, intravitreal injection of anti-VEGF agents are now emerging as part of first line treatment in AMD, RVO, and DME. In addition, they are already considered a valuable adjunct in other conditions such as PDR and NVG with ongoing studies that may further define their role and benefits. Antiangiogenic agents have been used successfully in the treatment of sickle cell retinopathy (Siqueira et al. 2006), retinopathy of prematurity (Altinsoy et al. 2010; Law et al. 2010), radiation retinopathy (Gupta and Muecke 2008) and other similar proliferative retinal vascular diseases. However, the long-term safety and potential toxicity of chronic VEGF inhibition needs to be closely monitored.
A large and rapidly expanding body of angiogenesis research is accumulating from the efforts of multiple investigators around the globe. This information is helping define specific roles for different angiogenic factors and improved treatment modalities and therapeutic regimens. The forthcoming availability of numerous highly specific antiangiogenesis agents and robust clinical trial data demonstrating remarkable efficacy is rapidly revising our current concept of standard care and holds great promise for improved management of these conditions in the near future.
Footnotes
Editors: Michael Klagsbrun and Patricia D'Amore
Additional Perspectives on Angiogenesis available at www.perspectivesinmedicine.org
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