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Program Book

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Patients in the triamcinolone group received periocular injection of<br />

triamcinolone acetonide (40 mg in 1 ml) at the time of plaque radiotherapy<br />

and 4-months and 8-months later. Optical coherence tomography (OCT)<br />

was performed at each patient evaluation.<br />

Results. OCT-evident macular edema occurred significantly less often in<br />

the triamcinolone group compared to the control group up to 36-months<br />

following plaque radiotherapy (relative risk 0.61, 95% CI 0.46-0.81). At<br />

36-month follow-up however, rates of moderate vision loss (loss of 3 or<br />

more lines of best corrected visual acuity [BCVA]) and severe vision loss<br />

(BCVA 10 mm in LBD) were included in this<br />

prospective study. Patients were scheduled for I-125 brachytherapy<br />

and randomized for adjuvant IVTA (4mg/0.1mL) or IVA (1.25mg/0.05mL)<br />

injection performed at plaque removal. All patients underwent a 1, 3, 6<br />

month follow-up examination, and every 6 months thereafter, including<br />

fundus photography and A/B scan ultrasonography. Follow-up was<br />

longer than 24 months.<br />

Results. Follow-up was 37±7 months. Tumour regression was<br />

achieved in all patients. Complete SRD regression was documented in<br />

eighteen IVTA- treated patients (56%) vs eleven IVA-treated patients<br />

(34%) (p

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