IRISS registry study offers real-world outcomes

The fluocinolone acetonide implant Iluvien (Alimera Sciences) maintained good real-world vision levels in patients with diabetic macular oedema (DMO) who had good baseline vision.

The open-label, observational Iluvien Registry Safety Study (IRISS)1 collected real-world data on the safety and efficacy of the 0.2 µg/day of fluocinolone acetonide implant for treating chronic DMO, defined as recurrent DMO that was insufficiently responsive to available therapies.

The DMO had been present for a mean of 4.95 years. The patients were followed from the time of implantation of the device to 3 years postoperatively, according to Dr Ramin Khoramnia of the David J. Apple International Laboratory for Ocular Pathology at the University Eye Clinic of Heidelberg, Germany.

A total of 295 patients (343 eyes; mean age, 66.3 years) were included in the study at 41 European sites. The mean baseline visual acuity (VA) was about 52 Early Treatment Diabetic Retinopathy Study letters.

Most eyes (97.7%) had undergone laser or intravitreal treatment. Patients had had an insufficient response to previous therapies before being treated with the implant – that is, they had been treated according to the licensed indication in Europe.

“Regarding supplemental therapies, 51.3% of Iluvien-treated eyes that had not optimally responded to previous therapy received no additional treatments during the 36 months,” Dr Khoramnia said. “This fact is particularly interesting because previous treatments had been suboptimal in terms of outcomes.”

During the 36-month study period, a mean of about 7.4 supplemental treatments were given; 11.1% of patients received a second implant after about 2.8 years following implantation, Dr Khoramnia noted. “The intraocular pressure [IOP] remained stable throughout the study and was in the normal range at every time point at which the patients were evaluated,” he said. About 40% of patients had IOP elevations that were managed medically; a surgical intervention was required to lower the IOP in 3.2% of eyes.

Stable/improved vision

Regarding VA outcomes, the VA required to drive (20/40) improved in 18.2% of eyes at baseline to 33% at 12 months and this level remained stable until the 36-month time point. In almost three-quarters of eyes (≥71%), the VA remained stable or improved over the 36 months. In eyes in which the baseline VA exceeded 20/40, the VA did not change significantly from baseline at any visit during the 3-year follow-up.

Dr Khoramnia concluded that for patients completing 3 years of follow-up, the real-life outcomes confirm the long-term safety and effectiveness of the implant for treating DMO in a cohort of patients larger than the European Union registration trial population. The results from clinical practice show changes in IOP and VA that are similar to those in the pivotal FAME trials.^1,2

“It is important to mention that real-world studies, especially those of DMO, rarely confirm the good outcomes of the pivotal trials,” he said. “The data also showed that earlier treatment of DMO in patients with better vision before the onset of substantial visual impairment stabilised vision for 3 years.”

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Ramin Khoramnia, MD
E: Ramin.Khoramnia@med.uni-heidelberg.de
This article is adapted from Dr Khoramnia’s presentation at the American Academy of Ophthalmology’s virtual 2020 annual meeting. He is a researcher for Alimera Sciences and receives lecture fees from the company.

References

1. Chakravarthy U, Taylor SR, Koch FHJ. ILUVIEN Registry Safety Study (IRISS) Investigators Group. Changes in intraocular pressure after intravitreal fluocinolone acetonide (ILUVIEN): real-world experience in three European countries. Br J Ophthalmol. 2019;103:1072–1077.
2. Campochiaro PA, Brown DM, Pearson A, et al. FAME Study Group. Sustained delivery fluocinolone acetonide vitreous inserts provide benefit for at least 3 years in patients with diabetic macular edema. Ophthalmology. 2012;119:2125-2132.