The Treatment Burden of Myopic Choroidal Neovascularization

Patients affected by treatment-naive mCNV will be included in a 12-month monocentric retrospective cohort study; all patients have been treated with intravitreal anti-VEGF injections between 2020 and 2024 in the Eye Clinic Policlinico Gaspare Rodolico, (Catania, Italy). The study adheres to the tenets of the Helsinki Declaration and ita has been approved by the Institutional review board of the University of Catania (Catania 1 Local Ethical Committee). Informed consent was given by patients at the start of the treatment.

Before starting the treatment, all patients have received a complete ophthalmic examination including a best-corrected visual acuity (BCVA) test, biomicroscopic slit-lamp examination, fundus examination in mydriasis, OCT and OCTA. All patients underwent one intravitreal injection at baseline (0.5 mg ranibizumab or 2.0 mg aflibercept); additional intravitreal injections were administered over the follow-up period according to the activity signs detected (pro-re-nata treatment protocol). Any signs of activity were detected by OCT and OCTA and fluorescein angiography has been performed whenever deemed necessary. Myopic active CNV was defined by clinical (retinal haemorrage detection on fundus examination) and OCT signs (intraretinal cysts, subretinal fluid and subretinal hyperreflective exudation with fuzzy borders). Fluorescein Angiography (FA) was performed .

Clinical and imaging data of the baseline examination and of the 12-month visit (M12) after the first intravitreal injection will be collected.

Best-corrected visual acuity was tested on standard Early Treatment Diabetic Retinopathy Study (ETDRS) charts converted into logarithmic scale of the minimal angle of resolution (logMAR). OCT and FA were carried out by Spectralis HRA+OCT with a confocal scanning laser ophthalmoscope (Heidelberg Engineering, Heidelberg, Germany). The OCT scan protocol used was a 15°x15° 67-section macular cube with additional high resolution horizontal and vertical single lines centred on the CNV. AngioVue XR Avanti (Optovue Inc, Fremont, California, USA) was employed to perform OCTA. A light source of 840 nm was used and the A-scan rate was 70,000 per second with a bandwidth of 50 nm. The macula images (6mmx6mm) obtained by OCTA were centered on the foveola. Each volume contained 400x400 A-scans with two consecutive B-scans acquired in each fixed position. The split-spectrum amplitude-decorrelation angiography (SSADA) method was used to capture the dynamic motion of red blood cells. mCNV areas were selected manually using AngioAnalytics software on the outer retina slab.

The values of the "CNV select area" will be included in the analysis as mCNV size. The Central Macular Thickness (CMT, micron) automatically provided by the machine, will be collected.

Myopic CNV will be categorized either as subfoveal (the CNV reaches the center of the fovea) or juxtafoveal (less than 200 micron from the center of the fovea) according to the location. In addition, mCNV will be categorized by OCTA features, either as immature (small-size, poorly structured neovascular network), or mature (larger and fully organized neovascular network) according to previous findings. Subretinal fibrosis (SF) will be defined as the detection at fundus examination of yellowish or greyish subretinal tissue in the foveal or parafoveal area, corresponding to an OCT image of a well-demarcated hyperreflective lesion situated between the retinal pigment epithelium and the neurosensory retina.

The number of in-hospital visits, invasive imaging examination (fluorescein angiography) as well as the number of intravitreal injections that underwent the patient will be collected and represent the burden of treatment.

The following clinical and imaging parameters will be included in the analysis: sex, age (years), anti-VEGF drug administered, mCNV location (subfoveal or juxtafoveal). BCVA (logMAR), CNV area (mm2), mCNV pattern will be assessed both at baseline visit and at 12-month visit. At the end of the follow-up period (12 months) will be assessed the presence of subretinal fibrosis (SF). The eyes will be categorized as stable (number of injections ≤ 2) or unstable (number of injections \> 2) according to the number of injections administered as previously reported).

All the data will be collected according to the above-mentioned criteria by using a standardized Excel spreadsheet (Microsoft Corp.). In case of lacking data the patient will be excluded from the study.

Statistical analysis will be performed by SPSS (version 22, IBM, New York, USA). Variables related to the number of injections at 12 months (dependent variable) will be tested in a univariate regression analysis; any variable with a p value \<0.2 in univariate analysis will be included in multivariate logistic regression analysis. Comparison of continuous variable values between two groups will be performed by unpaired t-test. Potential risk factors for more than 2 injections (unstable group) will be identified in univariate analyses, using the chi-square or Fisher exact tests for categorical variables, and Mann-Whitney tests for quantitative variables. Odd ratio will be calculated, and Exp(B) from binary logistic regression will be used for the continuous variables. P-values lower than 0.05 will be considered statistically significant.

• Visual Acuity [Time frame: one year]
• Intraretinal Cysts [Time frame: one year]
• Subretinal fluid [Time frame: one year]
• Subretinal fuzzy material [Time frame: one year]
• Subretinal fibrosis [Time frame: one year]
• Cnv maturity pattern [Time frame: one year]