Retrospective interventional case series.
PARTICIPANTS: The primary
cancer originated in the lung (n = 17 [39%]), breast (n = 16 [37%]), kidney (n = 3 [8%]), thyroid (n = 2 [6%]), and other sites (n = 5 [10%]). The mean patient age at entry was 61 years. Ocular symptoms included decreased visual acuity (n = 23 [53%]), visual field defect (n = 2 [5%]), floaters (n = 7 [16%]), flashes (n = 3 [7%]), and asymptomatic (n = 8 [19%]). The median entering visual acuity (Snellen equivalent) was 20/40. The median
tumor diameter was 5.0 mm, and median thickness by ultrasonography was 2.0 mm. The median distance to the optic disc was 3.0 mm, and that to the foveola was 2.0 mm. Of the 43 patients, 35 maintained follow-up (40 eyes, 45
tumors), and
PDT achieved
tumor control with 1 session (n = 32
tumors [71%]) or 2 sessions (n = 3
tumors [7%]) and failed to achieve regression (n = 10
tumors [22%]). The 10
metastases for which treatment failed were managed further with plaque
radiotherapy (n = 3),
proton beam
radiotherapy (n = 1), external beam
radiotherapy (n = 1), systemic
chemotherapy (n = 4), and observation (patient preference; n = 1). A comparison of clinical features for
tumor control (
PDT alone vs.
PDT plus additional
therapy) revealed those controlled with
PDT alone were more likely to be
adenocarcinoma (73% vs. 30%; P = 0.02) and those eyes were more like to achieve final visual acuity of 20/20 to 20/40 (66% vs. 30%; P = 0.03), with better median final Snellen visual acuity (20/30 vs. 20/70; not significant). Primary
cancer site or ocular
tumor features (size, location, color, shape, related subretinal fluid) did not impact
tumor control. In the entire group of 40 eyes, visual acuity improved or remained stable in 28 (70%) and decreased in 12 (30%), related to subfoveal
scar, persistent subretinal fluid, reactive exudation, radiation
maculopathy, and brain
metastasis. At last follow-up (mean, 20 months), of the entering 43 patients, 9 (21%) were alive and 34 (79%) had died of systemic
metastasis.
CONCLUSIONS: