Case Series Investigating the Efficacy and Safety of Bilateral Fluocinolone Acetonide (ILUVIEN^®) in Patients with Diabetic Macular Edema

Diabetic retinopathy (DR) is a visual complication that presents in around 35% of patients with diabetes [1]. A further visual complication manifesting in 6.8% of patients with DR is diabetic macular edema (DME), a chronic condition that results in significant reduction in vision and blindness in the working-age population [1]. DME can be unilateral or bilateral, with bilateral DME presenting in approximately 33–46% of patients with DME [2, 3]. Due to its chronic nature and persistence, DME can be difficult to manage, and without treatment nearly half of all patients who develop DME will lose two or more lines of visual acuity (VA) within 2 years [4, 5].

Historically, the standard of care for DME was laser therapy; however, vision gain following such treatment was limited [6]. More recently, several prospective randomized clinical trials have shown significant gains in VA in patients with DME following treatment with anti-vascular endothelial growth factor (VEGF) agents, resulting in a shift toward anti-VEGF treatment as the preferred standard of care and first line of treatment [6‐9]. Despite promising efficacy, however, results from the RIDE (ClinicalTrials.gov identifier, NCT00473382) and RISE (ClinicalTrials.gov identifier, NCT00473330) trials investigating the anti-VEGF agent, ranibizumab, found that patients who crossed over from sham to ranibizumab at 24 months were notably less responsive to treatment. These data are indicative of a subgroup of patients with longer-term chronic DME who may be insufficiently responsive to intermittent therapies such as the injection of anti-VEGF [8, 9].

Chronic DME is thought to be associated with a more inflammatory state following a shift in the expression of numerous inflammatory cytokines and VEGF-independent pathways responsible for its pathogenesis [10]. Consequently, chronic DME may require broader spectrum treatments such as corticosteroids, which have anti-inflammatory and angiostatic effects [11‐13].

ILUVIEN^® (Alimera Sciences Limited, Aldershot, UK) is an intraocular, nonbioerodible 0.2 μg/day fluocinolone acetonide (FAc) sustained-release implant that is approved in Europe for treatment of vision impairment associated with chronic DME considered insufficiently responsive to available therapies [14]. The Fluocinolone Acetonide in Diabetic Macular Edema (FAME; ClinicalTrials.gov identifier, NCT00344968) study compared 0.2 μg/day (the ultimately approved dosage) FAc with sham injections in patients with DME who were insufficiently responsive to the standard of care at that time, having received ≥1 focal laser treatment [15]. Three-year treatment with 0.2 μg/day FAc implant was associated with a significant improvement in vision outcomes, with the greatest benefit being reported in patients with chronic DME where 34.0% of patients treated with 0.2 μg/day FAc implant gained ≥15 in letter score at month 36 compared with only 13.4% of sham-treated patients [16]. However, the FAc implant was associated with increased intraocular pressure (IOP) compared with sham-treated patients and increased risk of cataract in patients who were phakic at baseline. As such, in the UK, National Institute for Care and Health Excellence (NICE) technology appraisal TA 301 recommends 0.2 μg/day FAc implant for pseudophakic patients with chronic DME that are deemed by the clinician to be insufficiently responsive to laser or anti-VEGF.

Little published data exist for treatment strategies in patients with bilateral chronic DME who are deemed insufficiently responsive to other therapies. Based on the NICE TA301 guidance, the 0.2 μg/day FAc implant in both eyes could be a sensible consideration for these patients in the UK setting. The summary of product characteristics for 0.2 μg/day FAc implant states that ‘Administration in both eyes concurrently is not recommended’. Nevertheless, concurrent use, with both eyes injected at different time points, is not contraindicated [14]. Moreover, pharmacokinetic data over 36 months demonstrated negligible systemic exposure to FAc following treatment with 0.2 μg/day FAc implant, highlighting its localized nature [14], which would suggest concurrent treatment would not present an unexpected side effect profile. This retrospective study investigates visual function, anatomical outcomes and safety of 0.2 μg/day FAc implant in both eyes of six patients with bilateral chronic DME.

This retrospective case series analysis assessed the visual function and anatomical measures at baseline and after a 6-month follow-up in six patients who received bilateral 0.2 μg/day FAc implants between April 2014 and October 2014. As a retrospective analysis, data were collected using case notes and optical coherence tomography (OCT) scans collected during treatment as part of the standard care pathway. Consequently, institutional review board policies did not necessitate additional ethics committee approval for this analysis.

Baseline demographics were collected from patient records at the time of 0.2 μg/day FAc implant and included age, gender, general health, and disease and treatment history. In addition, Snellen VA (at 6 m) and anatomical measures using optical coherence tomography [e.g., central retinal thickness (CRT), central subfield foveal thickness (CSFT)] were noted at baseline. Snellen VA was converted into approximate Early Treatment Diabetic Retinopathy Study (ETDRS) letters to facilitate interpretation using the following equation: 85 + 50 × log (Snellen fraction), as described by Gregori et al [17].

Efficacy assessments at 6-month follow-up included changes in VA, anatomical measures (including CRT and CSFT), and in the number of fields out of 9 over 300 μm thickness. In addition, safety was evaluated through collection of data on changes in IOP and any other recorded complications.

This study evaluated the bilateral injection of 0.2 μg/day FAc implant in six patients with DME in both eyes in the real-world setting. All eyes had received ≥1 macular laser treatment and ≥3 ranibizumab injections and were deemed insufficiently responsive to these treatments. Ten eyes had also received ≥1 IVTA injection prior to 0.2 μg/day FAc implant. The average CRT at baseline was high (648 μm) and most eyes (10/12) had baseline BCVA below 70 letters (6/12), the minimum requirement for maintaining a driving license in Europe [18]. Six months post-0.2 μg/day FAc implant, 58.3% of eyes had gained >10 letters and 41.7% ≥15 letters. Although the patient numbers are small, these values are consistent with outcomes reported in the FAME studies, where 51.7% of eyes treated with 0.2 μg/day FAc implant gained >10 letters [19] and 34% gained ≥15 letters [16]. Four patients had achieved or maintained driving vision and there was a notable reduction in CRT in all eyes with a baseline CRT >600 μm. This is an important outcome in the management of DME progression, as prolonged edema results in irreversible damage and permanent vision loss, emphasizing the need for early intervention [20]. Further, minimal increases in IOP were observed and no patients needed to initiate IOP-lowering medication post-0.2 μg/day FAc implant.

Of the six patients who received bilateral 0.2 μg/day FAc implant in this study, five had severe edema with CRT >600 μm in both eyes, in addition to low VA below driving vision after multiple prior treatments with macular laser, ranibizumab, and IVTA. Further, all eyes had foveal eversion on OCT. Taken together, these data suggest that, in a real-world setting, clinicians selected patients with severe bilateral DME for 0.2 μg/day FAc implant in both eyes. It is accepted that early intervention and management of DME is important in minimizing vision loss and maintaining the quality of life in patients with DME; this is perhaps even more important when both eyes are affected, increasing the risk of legal blindness. Further sub-analyses of the RISE and RIDE trials with ranibizumab found that patients with chronic DME may become refractory to anti-VEGF therapy once DME disease progresses [9]. If, as some evidence suggests [10], this is associated with a more complex inflammatory cytokine state, treatment with corticosteroids may be appropriate at an earlier stage in patients with chronic DME. In the FAME trials, the sustained and localized release of 0.2 μg/day FAc implant resulted in improved visual and anatomical outcomes that were maintained for up to 36 months [16]. However, the proportion of patients with chronic DMO that achieved driving vision following 0.2 μg/day FAc implant was reduced in patients with lower baseline VA, highlighting the importance of early treatment for optimal visual outcomes [21]. Consequently, in patients with bilateral DME, treatment of both eyes with 0.2 μg/day FAc implant may be beneficial and, as it is not contraindicated, should be considered.

This study demonstrates the potential efficacy of 0.2 μg/day FAc implant in both eyes of patients with bilateral DME. CRT was consistently reduced in all but two eyes, which had relatively low CRT values and good VA at baseline, and four eyes maintained or achieved driving-level vision. There was no notable increase in IOP and no additional IOP-lowering treatment required following 0.2 μg/day FAc implant; no other treatment-related complications were reported. These data suggest that it is safe to carry out bilateral 0.2 μg/day FAc implant in patients with DME in both eyes, with potential improvements in DME and in the management of the long-term negative impact of DME-mediated vision loss. This is the first case series that the authors are aware of, to demonstrate the feasibility of bilateral 0.2 μg/day FAc implant in a real-world setting, and it suggests that, in patients with bilateral DME insufficiently responsive to alternative therapies, bilateral 0.2 μg/day FAc implant should be considered.