Radiation retinopathy following plaque radiotherapy for posterior uveal melanoma


Gündüz K., Shields C., Shields J., Cater J., Freire J., Brady L.

ARCHIVES OF OPHTHALMOLOGY, cilt.117, sa.5, ss.609-614, 1999 (SCI-Expanded, Scopus) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 117 Sayı: 5
  • Basım Tarihi: 1999
  • Doi Numarası: 10.1001/archopht.117.5.609
  • Dergi Adı: ARCHIVES OF OPHTHALMOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.609-614
  • Ankara Üniversitesi Adresli: Evet

Özet

Objective: To identify the risk factors that lead to the development of radiation retinopathy following plaque radiotherapy for posterior uveal melanoma. Radiation retinopathy is a slowly progressive, occlusive vasculopathy characterized by radiation-induced endothelial damage. Methods: Review of the medical records of patients with posterior uveal melanoma 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 retinopathy developed in 560 (43.1%). By using Kaplan-Meier survival estimates, we found 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%). Multivariate 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 mellitus (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 radiotherapy 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.