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. 2017 Feb 17;31(6):890–898. doi: 10.1038/eye.2017.7

Aflibercept as a Second Line Therapy for Neovascular Age Related Macular Degeneration in Israel (ASLI) study

L Tiosano 1, O Segal 2,10, N Mathalone 3,10, A Pollack 4, R Ehrlich 5, I Klemperer 6, Y Barak 7, I Moroz 8, I Chowers 1,*, M Goldstein 9
PMCID: PMC5518842  PMID: 28211882

Abstract

Purpose

The purpose of this study is to evaluate an early switch to aflibecept in eyes with neovascular age-related macular degeneration (nvAMD) showing partial or lack of response for initial therapy with bevacizumab.

Methods

The Aflibercept as a Second Line Therapy for Neovascular Age Related Macular Degeneration in Israel (ASLI) was a prospective, multicenter, single-arm clinical trial. Eyes with nvAMD having incomplete response to 3–9 prior bevacizumab injections were recruited. Three monthly intravitreal aflibercept (2 mg) injections were administered, followed by two bi-monthly injections and a final examination at week 28. An optional injection was allowed at week 20.

Results

Forty-seven eyes of 46 patients (mean±SD age 76±8 years) were recruited. The mean number of prior bevacizumab injections was 5.5±2.9. The mean visual acuity improved from 60.3±10 ETDRS letters at baseline to 63.1±15 letters at week 28 (P=0.02, paired t-test). The central subfield thickness (CST) reduced from 409±127 micron at baseline to 330±110 microns at week 4 (P=0.0002; paired t-test), and 277±70 microns at week 28 (P=0.00002; paired t-test). Twenty-two eyes had three to five prior bevacizumab injections (mean 5.1±0.7), and 25 eyes had six to nine prior injections (7.32±1.2). Both groups had reduced CST from baseline to week 28 (P=0.0004 and P=0.0007; paired t-test, respectively). Thirty-five (75%) eyes required the optional additional aflibercept injection at week 20.

Conclusions

The ASLI study demonstrated improved BCVA and reduced CST following an early switch to aflibercept therapy in eyes with prior incomplete response to initial therapy with three to nine bevacizumab injections.

Introduction

Anti-VEGF compounds, administered intravitreally, markedly improved the short- and intermediate-term outcome of neovascular age-related macular degeneration (nvAMD). On the basis of several prospective multicenter clinical trials, it was concluded that non-inferior visual outcome is obtained when either ranibizumab or bevacizumab is applied for treating nvAMD.1, 2, 3, 4, 5 The VEGF-Trap Eye Investigation of Efficacy and Safety in Wet AMD (VIEW) 1 and VIEW 2 trials also described similar visual outcome following either ranibizumab or aflibercept treatment for nvAMD.6, 7, 8

Aflibercept is a recombinant fusion protein consisting of the key human VEGF receptor extracellular domains from receptors 1 and 2 (VEGFR1 and VEGFR2) fused to the Fc domain of human IgG1.9 Aflibercept is different from bevacizumab and ranibizumab by having higher binding affinity for VEGF-A by binding to placental growth factors 1 and 2 (PLGF1 and PLGF2) and VEGF-B, and by having a longer half-life in the vitreous (compared to ranibizumab).7, 10 While, overall, bevacizumab, ranibizumab, and aflibercept obtain similar treatment outcome in nvAMD, differences among these compounds may affect treatment outcome in the subgroup of patients. The VIEW 1 and VIEW 2 studies demonstrated that aflibercept administered every 2 months following three initial monthly loading doses was non-inferior to monthly ranibizumab in maintaining vision in patients with treatment-naive nvAMD over 1 year.6 Yet, a recent study reported that a more frequent injection schedule may be required in some of the cases.11

Despite the similar overall efficacy, when unsatisfactory response is observed following treatment with a single anti-VEGF compound, a switch to one of the other available anti-VEGF drugs is often performed. This strategy is based on several reports, suggesting anatomic and visual outcome benefits following switching between anti-VEGF therapies in cases of unfavorable response to the first-line treatment.8, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33

According to the program of the Israeli Ministry of Health, off-label bevacizumab serves as the first-line therapy for nvAMD in the majority of nvAMD cases. Guidelines for the preferred timing and benefit of switch to a second-line therapy for nvAMD were not developed at the inception of this study. In many cases, such second-line treatment is initiated only after multiple previous injections of the first-line compound. By that time a substantial visual loss and structural macular damage have already occurred. Conceivably, an early switch, when irreversible damage to foveal tissue is still limited, may yield improved outcome.

To further assess the efficacy of aflibercept as an early second-line therapy in nvAMD, we have conducted a multicenter prospective clinical trial in nvAMD patients with lack or incomplete response to prior first-line bevacizumab treatment.

Materials and methods

Study design

The Aflibercept as Second Line treatment in Israel (ASLI) study was a prospective, multicenter, open label, single-arm clinical trial that was initiated by the Israeli Retina Society. Forty-six patients (47 eyes) were enrolled during 12 months from April 2014 through April 2015 at eight clinical centers around Israel. All patients were followed for 28 weeks. The study was approved by the institutional review board at each participating clinical center, and all patients provided written informed consent. The ASLI study was registered with ClinicalTrials.gov (identifier no. NCT01918878).

Participants

Inclusion criteria for the study eye included incomplete or no response to first-line intravitreal injections of bevacizumab for nvAMD. First-line treatment was provided in the setting of a clinic prior to recruitment to the ASLI trial. Incomplete or no response was defined based on OCT criteria that included the presence of intra- or subretinal fluid (IRF, SRF), and/or pigment epithelium detachment (PED) with maximal central point thickness of 300 microns or larger (retinal thickness including SRF, IRF, and PED) according to the Heidelberg OCT. We included patients who received between three and nine bevacizumab injections within the first year from diagnosis of new onset choroidal neovascularization (CNV) secondary to AMD. The intervals between each of the last three injections had to be no longer than 6 weeks. This interval was chosen as it reflected real-life clinic setting treatment interval, and since it was considered acceptable at the time.34, 35, 36, 37, 38 Best-corrected visual acuity (BCVA) in the study eye was between 30 and 80 letters of Early Treatment Diabetic Retinopathy Study (ETDRS) visual acuity chart (Snellen equivalent of ~20/40 to 20/360). Inclusion imaging criteria were based on optical coherence tomography (OCT) and fluorescein angiogram (FA) performed at the screening visit. FA inclusion criteria included total area of the lesion (including leakage, blood, and scar/atrophy) smaller than five disc areas, of which at least 50% must be active CNV. Exclusion criteria included presence of any pathology, other than nvAMD, that could be associated with the development of CNV, more than 50% of the total lesion size consisting of subretinal hemorrhage, presence of retinal angiomatous proliferation, or RPE tears. Active or suspected ocular or periocular infection or inflammation, clinically significant epiretinal membrane, vitreomacular traction, macular hole, or vitreous hemorrhage were other exclusion criteria. Eyes with uncontrolled intraocular pressure (IOP) or any intraocular surgery or thermal laser within 3 months of trial entry were also excluded.

Study protocol

BCVA and imaging (OCT and FA) were performed following a standardized protocol. OCT images from the screening visit were reviewed by the site's PI. FA images were analyzed by a centralized reading center that reviewed all FAs to determine eligibility (MG). To approve eligibility for the study, the FA had to be deemed eligible by the reading center, and the clinical details and OCT images had to be reviewed by additional two PIs from other participating centers. A unanimous consensus was required to confirm participation of the patients in the study.

Loading dosage composed of three monthly intravitreal aflibercept (2 mg; day 0, week 4, and week 8) was followed by further injections of aflibercept at weeks 16 and 24. In cases where IRF and/or SRF were detected at week 16, an additional injection was provided at week 20 per the investigator's discretion. Thus, a total of five to six aflibercept injections were administered during the study period.

At each visit, a full ophthalmic examination, including protocol BCVA and IOP assessment with Goldman applanation tonometry, adverse event monitoring, and SD-OCT/ HD-OCT (Heidelberg Spectralis; Heidelberg Engineering, Heidelberg, Germany, or Ziess cirrus, Carl Zeiss Meditec, Dublin, CA, USA), measurement of both eyes was conducted with appropriate correction factors of adding 10 microns to the thickness for measurements that were based on Cirrus HD-OCT to compare thickness to the Spectralis SD-OCT.39 FA was performed at the baseline at the last visit.

Statistical analysis

Statistical analysis was performed using SPSS (version 21.0; SPSS Inc., Chicago, IL, USA). Study sample was calculated using Hochberg’s procedure to control the type I error rate for the primary end point at 5% (two-sided), and provide 80% probability that the change in the central subfield thickness (CST) will be significant. Measures of BCVA, CST, and maximal central thickness were summarized using means, SDs, median, and range. Since the data were normally distributed, comparisons with and between groups for BCVA and CST parameters were performed using two-sided t-tests. Where appropriate, sensitivity analysis using nonparametric Wilcoxon-signed rank tests was also performed. A P-value of less than 0.05 was considered significant.

Results

Baseline patient characteristics and patient retention

Forty-seven eyes of 46 patients were enrolled to the study in eight academic medical centers around Israel. The mean±SD age at baseline was 76±8 years, and 28 (61%) patients were female. Twenty-two eyes had three to five prior bevacizumab injections (mean±SD 5.1±0.7), and 25 eyes had six to nine prior injections (mean±SD 7.32±1.2). Baseline characteristics are presented in Table 1.

Table 1. Baseline characterization of patients enrolled within the ASLI study (n=47).

Age (years) mean±SD 76±8
Female/male (%) 61/39
 
Previous bevacizumab treatment, number (%)
 3 15 (32%)
 4 4 (8%)
 5 3 (6%)
 6 9 (19%)
 7 7 (15%)
 8 1 (2%)
 9 8 (17%)
 
Vitreoretinal interface, number (%)
 Attached vitreous 18 (38%)
 PVD 15 (32%)
 ERM 1 (2%)
 VMT 1 (2%)
 
Drusen type, number (%)
 Typical AMD 36 (77%)
 Cuticular 3 (6%)
 Subretinal drosenoid 3 (6%)
 
Retinal fluid, number (%)
 SRF 33 (70%)
 IRF 18 (38%)
 PED 21 (45%)
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Abbreviations: AMD, age-related macular degeneration; ERM, epiretinal membrane; IRF, intraretinal fluid; PED, pigment epithelium detachment; PVD, posterior vitreous detachment; SRF, subretinal fluid; VMT, vitreomacular traction.

One patient was withdrawn from the study at week 16 because of unsatisfactory response according to the discretion of the treating PI. This patient manifested exacerbation of PED and adjacent subretinal fluid despite 3 monthly injections of afllebercept. One patient did not receive the treatment at week 16 because of an active herpes simplex keratitis in the study eye. When the infection resolved, the remaining treatments were provided as scheduled. Three ocular adverse events were observed, one eye had retinal detachment during the follow-up, and two eyes had transient elevated IOP. One patient experienced bowel obstruction, which was treated medically without the need for surgery.

Anatomic outcome

The CST reduced during the study from a mean±SD of 409±127 microns at baseline to 330±100 microns (P=0.0002) at week 4 and 277±70 microns (P=0.00002; paired t-test) (Figure 1a) at week 28. Following the first bi-monthly interval between the week 8 and week 16 visits, there was an increase in CST from 324±112 to 358±125 microns (P=0.003; paired t-test). Overall, 35 (75%) eyes received the optional injection at week 20. The CST remained stable in the 12 eyes that received only the two bi-monthly injections at weeks 16 and 24 (Figure 1b).

Figure 1.

Figure 1

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The mean change in CST in microns according to OCT during 28 weeks of follow-up (n=47; a). (b–c) A subgroup analysis of CST changes during the study. (b) CST changes in eyes that received additional injection at week 20 (n=35) and eyes without additional injection (n=12). There were similar CST changes in both groups. (c) CST changes along the study according to the number of bevacizumab injections prior to enrollment to the study. There were similar CST changes in both groups. *P<0.05 for the comparison of baseline vs follow-up examination in the same group. Error bars represent SEM.

Subgroup analysis for 22 eyes that had three to five prior bevacizumab injections, and 25 eyes with prior six to nine injections demonstrated reduction in CST in both groups from mean±SD of 407±145 and 405±107 microns at baseline to 280±84 and 272±51 microns at week 28 (P=0.0004 and P=0.0007, respectively; paired t-test; Figure 1c). Both groups demonstrated similar visual outcome during the follow-up (Figure 1c).

Thirty-three (70%) eyes had SRF at presentation, while only 12 (25%) eyes had SRF at week 28 (P=0.01). Only four (8%) eyes had IRF at week 28 compared with 18 eyes (38%) at baseline (P=0.01). PED was present in 18 eyes (38%) at week 28 compared with 21 eyes (45%) at baseline (P=0.8).

Visual acuity outcome

BCVA score improved during the study from mean±SD at baseline of 60.3±10 to 63.1±15 letters at the end of the follow-up (P=0.02; paired t-test; Figure 2a). At week 28, 21 (45%) eyes improved by five letters or more and three (6%) eyes improved by 15 letters or more. Thirteen (28%) eyes lost one or more letter. Six (12%) eyes lost less than five ETDRS letters, three (6%) eyes lost 5–15 letters, and four (8%) eyes lost more than 15 letters during the study. Subgroup analysis identified no difference in visual outcome between the 35 eyes that had additional injection at week 20 and the remaining 12 study eyes (P=0.73; Figures 2b and 3). Subgroup analysis for 22 eyes with three to five prior bevacizumab injections demonstrated significant BCVA improvement from 60.4±11.2 at baseline to 62.8±18.7 ETDRS letters at week 28 (P=0.04; paired t-test). A trend of BVCA improvement was detected for the 25 eyes with prior six to nine injections from 62.9±8.5 ETDRS letters at baseline to 65.2±11.6 ETDRS letters at week 28 (P=0.23; paired t-test; Figure 2c).

Figure 2.

Figure 2

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The mean change in BCVA measured by ETDRS letters (n=47) during the study period (a). (b–c) A subgroup analysis of the mean change in BCVA during the study. (b) BCVA changes in eyes that received additional injection at week 20 (n=35), and in eyes without additional injection (n=12). (c) BCVA changes along the study according to the number of bevacizumab injections prior to enrollment to the study. There were similar BCVA changes in both groups. *P<0.05 for the comparison of current vs follow-up examination. Error bars represent SEM.

Figure 3.

Figure 3

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Seventy-four-year-old female who previously received five bevacizumab injections had SRF, IRF, and PED at baseline (a). Following the first aflibercept injection there was complete absorption of the IRF and minimal remnants of SRF (b), which resolved at week 8 (c). However, after the first bi-monthly interval, at week 16 there was recurrence of SRF and IRF (d). At week 20 there was a resolution of the fluid (e) and the macula remained dry until the end of the study under monthly therapy.

Discussion

In this prospective multicentre study, intravitreal aflibercept therapy as an early second-line therapy following bevacizumab failure yielded anatomical and functional improvement. The mean macular thickness reduced by over 100 micron and qualitative OCT parameters improved. The mean visual acuity increased by one ETDRS line or more in 45% of patients.

Multiple authors described outcomes after aflibercept therapy in cases of incomplete response to prior therapy with bevacizumab or ranibizumab in nvAMD.8, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 31, 32, 33 Recently, Lazzeri et al40 summarized these studies. Of the 21 studies identified, 16 were retrospective and 5 were prospective.14, 17, 21, 26, 32 Unlike the ASLI study, the majority of patients in the previous prospective studies were treated with first-line ranibizumab and because of partial response were switched to aflibercept. These prospective studies included all together 157 eyes with a follow-up period of 6–12 months. The mean number of anti-VEGF injections prior to the switch to aflibercept was 30, as opposed to our study in which the number was significantly lower (between three and nine). There were large variations in the number of prior injections within studies. Overall, the prospective studies reported a mean reduction of ~50 microns in macular thickness at 6 months and a mean improvement of four letters in the three studies who reported ETDRS visual acuity.40

Sarao et al30 recently reported another prospective study that was not included in the meta-analysis of Lazzeri et al.40 In this relatively large study (n=92), similar to our finding, an improvement of 1.8 letters in visual acuity and reduction in CST of over 100 microns was reported. Eyes were treated with aflibercept following an initial PRN protocol with ranibizumab injections and monthly monitoring and an average of 3.5 injections during 12 months of follow-up.30 Prior to switching to aflibercept, these eyes received an average of ~15 injections during 18 months of therapy.

Overall, results of these previous prospective studies are in accordance with our findings. The current trial provided additional important insights into second-line aflibercept treatment. Unlike previous prospective studies, the ASLI trial focused on systematic assessment of early conversion to second-line aflibercept and of the required treatment interval period in such eyes. Such early conversion may theoretically prevent the atrophic macular changes and scar formation, which are often observed in eyes with persistent CNV activity. Despite this theoretical advantage, the magnitude of visual gain in our study is in the same order of previous studied where second-line therapy was initiated after longer periods of first-line therapy. Furthermore, there was no difference in outcome between eyes with less3, 4, 5 or more6, 7, 8, 9 prior bevacizumab injections within the ASLI trial. Thus, conceivably, the benefit of early rather than delayed conversion to aflibercept is not reflected in the absolute visual gain following the conversion. Yet, it is likely that early conversion to successful second-line therapy may result in better outcome by avoiding the visual loss, which occurs during the time period of treatment with less-effective therapy for the particular eye.

According to its label for treatment of nvAMD, three monthly intravitreal injections of aflibercept are initially provided followed by bi-monthly injections. We have adopted this treatment schedule but also allowed for a rescue treatment at week 20, following the initial bi-monthly interval in cases where IRF and/or SRF were detected at week 16. Interestingly, we have found that average macular thickness increased after the first bi-monthly injection and that more than half of the patients required monthly aflibercept injection during the first 6 months of second-line therapy. Accordingly, it was recently suggested that bi-monthly aflibercept may not be sufficient in some of the nvAMD patients who receive this compound as a first-line therapy.11

The main caveats of our study is the lack of a control group, the small number of patients and relatively short follow-up period. It is not possible to assure that similar anatomical and visual gains will not be detected following longer treatment with first-line therapy, or following strict q4-week treatment schedule with bevacizumab. Furthermore, we have evaluated patients at week 28, 4 weeks rather than 8 weeks after the last aflebercept injection, a factor that may have also favorably affected outcome. Yet, as mentioned above, previous prospective studies that enrolled eyes following longer period of prior first-line therapy also reported visual gain similar to the ASLI trial once conversion to aflibercept treatment was performed. Thus, it is likely that conversion can at least shorten the time interval for visual improvement in eyes with incomplete response to first-line therapy.

In conclusion, in the ASLI study, aflibercept yielded both anatomical and functional benefits following incomplete response to first-line bevacizumab therapy in nvAMD. Further studies should explore the benefit of second-line anti-VEGF therapies to provide data that facilitate the establishment of treatment protocols designed according to evidence-based data.

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Acknowledgments

The study was partially funded by Bayer. The study medication was provided by Bayer.

Disclaimer

The conception and conduct of the study as well as the analysis of the data were performed independently by the authors and the company had no control over the data.

Footnotes

Dr Chowers serves as consultant for Lycored, Biokine, Bayer, and Novartis; Dr Goldstein serves as a consultant and invited lecturer for Novartis, Allergan, and Bayer; and Dr Polack serves as a consulted for Allergan and Bayer. The remaining authors declare no conflict of interest.

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