Objective: To identify the risk factors that lead to the development of rad
iation retinopathy following plaque radiotherapy for posterior uveal melano
ma. Radiation retinopathy is a slowly progressive, occlusive vasculopathy c
haracterized by radiation-induced endothelial damage.
Methods: Review of the medical records of patients with posterior uveal mel
anoma treated with plaque radiotherapy.
Results: Of 1300 patients with posterior uveal melanoma treated with plaque
radiotherapy from July 1, 1976, through June 30, 1992, radiation retinopat
hy developed in 560 (43.1%). By using Kaplan-Meier survival estimates, we f
ound that 5% of the patients had nonproliferative radiation retinopathy at
1 year (95% confidence interval [CI], 3%-6%) and 42% at 5 years (95% CI, 38
%-45%). The proportion of patients with proliferative retinopathy was 1% at
1 year (95% CI, 0.2%-1.5%) and 8% at 5 years (95% CI, 5%-10%). Multivariat
e analyses showed that the subset of clinical variables best related to the
development of nonproliferative radiation retinopathy were tumor margin of
less than 4 mm from foveola (P<.001), tumor limited to the choroid (P=.002
), and radiation dose rate of greater than 260 cGy/h to the tumor base (P=.
02). The best subset of independent variables related to the development of
radiation maculopathy were tumor of less than 4 mm to foveola (P<.001) and
the use of radioisotope iridium 192 (Ir-192) (P=.02) compared with iodine
125 (I-125). From a multivariate model, the most important factors for the
development of proliferative radiation retinopathy included diabetes mellit
us (P=.01), radioisotope Ir-192 (P=.01) compared with I-125, and tumor base
of greater than 10 mm (P=.02).
Conclusions: Radiation retinopathy is a common finding after plaque radioth
erapy for choroidal melanoma, occurring in 42% of patients at 5 years. The
main predictors of radiation retinopathy are posterior tumor location with
margin near the foveola and high radiation dose rate to the tumor base.