TY - JOUR
T1 - Risk Factors for Radiation Maculopathy after Ophthalmic Plaque Radiation for Choroidal Melanoma
AU - Finger, Paul T.
AU - Chin, Kimberly J.
AU - Yu, Guo Pei
N1 - Funding Information:
Supported by The Eye Cancer Foundation, Inc, New York, New York (P.T.F., K.C.); and The New York Eye and Ear Infirmary Research Fund, New York, New York (P.T.F.). The authors indicate no financial conflict of interest. Involved in Design of study (P.T.F.); Conduct of study (P.T.F., K.C.); Collection, management, analysis, and interpretation of data (P.T.F., K.C., G.Y.); and Preparation, review, or approval of the manuscript (P.T.F., K.C., G.Y.). This study adhered to the tenets of the Declaration of Helsinki and the Health Insurance Portability and Accountability Act of 1996. This study was also approved by the Institutional Review Board of The New York Eye Cancer Center.
PY - 2010/4
Y1 - 2010/4
N2 - Purpose: To determine how tumor characteristics and radiation dose affect the incidence of radiation maculopathy (RM). Design: Retrospective, consecutive case series. Methods: A consecutive case series of 384 uveal melanomas irradiated (mean apical dose, 71.2 Gy) were followed up for a mean 47.2 months. Tumor locations included: 122 (32%) centered anterior to the equator, 27 (7%) equatorial, and 235 (61%) posterior. Tumor sizes were American Joint Committee on Cancer class T1 (n = 180), T2 (n = 150), T3 (n = 47), and T4 (n = 7). Results: RM occurred in 8 (7%) eyes with anterior uveal melanomas. In contrast, it was found in 82 (41%) eyes with posterior tumors. Multivariate analysis revealed the risk related to posterior location was greater compared with anterior location with a hazard ratio of 6.66 (95% confidence interval [CI], 4.94 to 22.50; P = .0001). Tumor height (> 6.0 mm) also demonstrated a high risk for RM (hazard ratio, 4.5; 95% CI, 2.68 to 10.17; P = .0001). A significant dose-response relationship was found between dose to fovea and RM (P = .0005, for trend). As compared with a dose of < 35 Gy, the risk of RM was 1.74 (95% CI, 0.98 to 3.1) for doses from 35 to 70 Gy, and the risk of RM was 2.43 (95% CI, 1.48 to 4.0) for doses of 70 Gy or more. Of interest, those anterior melanomas with RM had a mean apical height of 9.4 mm, as compared with a mean height of 3.3 mm for anterior tumors not associated with RM. Visual acuity was preserved if the fovea dose was less than 35 Gy. Conclusions: This study suggests that tumor location, tumor thickness, and radiation dose to the fovea are risk factors for the development of RM.
AB - Purpose: To determine how tumor characteristics and radiation dose affect the incidence of radiation maculopathy (RM). Design: Retrospective, consecutive case series. Methods: A consecutive case series of 384 uveal melanomas irradiated (mean apical dose, 71.2 Gy) were followed up for a mean 47.2 months. Tumor locations included: 122 (32%) centered anterior to the equator, 27 (7%) equatorial, and 235 (61%) posterior. Tumor sizes were American Joint Committee on Cancer class T1 (n = 180), T2 (n = 150), T3 (n = 47), and T4 (n = 7). Results: RM occurred in 8 (7%) eyes with anterior uveal melanomas. In contrast, it was found in 82 (41%) eyes with posterior tumors. Multivariate analysis revealed the risk related to posterior location was greater compared with anterior location with a hazard ratio of 6.66 (95% confidence interval [CI], 4.94 to 22.50; P = .0001). Tumor height (> 6.0 mm) also demonstrated a high risk for RM (hazard ratio, 4.5; 95% CI, 2.68 to 10.17; P = .0001). A significant dose-response relationship was found between dose to fovea and RM (P = .0005, for trend). As compared with a dose of < 35 Gy, the risk of RM was 1.74 (95% CI, 0.98 to 3.1) for doses from 35 to 70 Gy, and the risk of RM was 2.43 (95% CI, 1.48 to 4.0) for doses of 70 Gy or more. Of interest, those anterior melanomas with RM had a mean apical height of 9.4 mm, as compared with a mean height of 3.3 mm for anterior tumors not associated with RM. Visual acuity was preserved if the fovea dose was less than 35 Gy. Conclusions: This study suggests that tumor location, tumor thickness, and radiation dose to the fovea are risk factors for the development of RM.
UR - http://www.scopus.com/inward/record.url?scp=77949652856&partnerID=8YFLogxK
U2 - 10.1016/j.ajo.2009.11.006
DO - 10.1016/j.ajo.2009.11.006
M3 - Article
C2 - 20138602
AN - SCOPUS:77949652856
SN - 0002-9394
VL - 149
SP - 608
EP - 615
JO - American Journal of Ophthalmology
JF - American Journal of Ophthalmology
IS - 4
ER -