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黄斑受累的脉络膜黑色素瘤敷贴放疗后的放射并发症及肿瘤控制情况

Radiation complications and tumor control after plaque radiotherapy of choroidal melanoma with macular involvement.

作者信息

Gündüz K, Shields C L, Shields J A, Cater J, Freire J E, Brady L W

机构信息

Oncology Service, Wills Eye Hospital, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

出版信息

Am J Ophthalmol. 1999 May;127(5):579-89. doi: 10.1016/s0002-9394(98)00445-0.

Abstract

PURPOSE

To determine the outcome of plaque radiotherapy in the treatment of macular choroidal melanoma and to identify the risk factors associated with the development of radiation complications, tumor recurrence, and metastasis.

METHODS

Chart analysis of 630 consecutive patients (630 eyes) with macular choroidal melanoma managed by plaque radiotherapy between July 1976 and June 1992.

RESULTS

The median largest basal tumor diameter was 10 mm, and the median tumor thickness was 4 mm. By means of Kaplan-Meier estimates, visually significant maculopathy developed at 5 years in 40% of the patients, cataract in 32%, papillopathy in 13%, and tumor recurrence in 9%. Vision decrease by 3 or more Snellen lines was found in 40% of the patients at 5 years. Sixty-nine eyes (11%) were enucleated because of radiation complications and recurrence. Twelve percent of the patients developed metastasis by 5 years and 22% by 10 years. Results of multivariate Cox proportional hazards analyses showed that the significant predictors for tumor recurrence were a distance of tumor margin from the optic disk of less than 2 mm (P = .003) and retinal invasion (P = .009). The significant variables that were predictive of metastasis included tumor thickness greater than 4 mm (P = .02) and largest basal tumor diameter greater than 10 mm (P = .03).

CONCLUSIONS

Plaque radiotherapy offers a 91% 5-year local tumor control rate for macular choroidal melanoma. Despite good local tumor control, the risk for metastasis is 12% at 5 years and 22% at 10 years. In 11% of the patients, enucleation eventually became necessary because of radiation complications and tumor recurrence.

摘要

目的

确定敷贴放射疗法治疗黄斑部脉络膜黑色素瘤的疗效,并识别与放射性并发症、肿瘤复发和转移发生相关的危险因素。

方法

对1976年7月至1992年6月间连续接受敷贴放射疗法治疗的630例(630只眼)黄斑部脉络膜黑色素瘤患者进行病历分析。

结果

肿瘤最大基底直径中位数为10mm,肿瘤厚度中位数为4mm。采用Kaplan-Meier法估计,40%的患者在5年时出现有视觉意义的黄斑病变,32%出现白内障,13%出现视乳头病变,9%出现肿瘤复发。在5年时,40%的患者视力下降3行或更多Snellen视力表行数。69只眼(11%)因放射性并发症和复发而被摘除眼球。12%的患者在5年时发生转移,22%在10年时发生转移。多因素Cox比例风险分析结果显示,肿瘤复发的显著预测因素为肿瘤边缘距视盘小于2mm(P = 0.003)和视网膜浸润(P = 0.009)。预测转移的显著变量包括肿瘤厚度大于4mm(P = 0.02)和肿瘤最大基底直径大于10mm(P = 0.03)。

结论

敷贴放射疗法为黄斑部脉络膜黑色素瘤提供了91%的5年局部肿瘤控制率。尽管局部肿瘤控制良好,但5年时转移风险为12%,10年时为22%。11%的患者最终因放射性并发症和肿瘤复发而需要摘除眼球。

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