Ophthalmic Oncology, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
Ophthalmology. 2011 Sep;118(9):1881-5. doi: 10.1016/j.ophtha.2011.01.040. Epub 2011 Jun 24.
To determine trends in incidence, treatment, and survival with primary uveal melanoma in the United States over a 36-year period from 1973 to 2008.
Systematic review of existing databases.
A total of 4070 patients with primary uveal melanoma (International Classification of Disease for Oncology [ICD-O-2] codes C69.3 [choroid], C69.4 [ciliary body and iris], and C69.2 [retina]) derived from the Surveillance, Epidemiology, and End Results (SEER) program database in the United States from 1973 to 2008.
The significance of trends in age-adjusted incidence, treatment, and 5-year relative survival rates were determined using chi-square testing and 95% confidence intervals (CIs).
Age-adjusted incidence, form of treatment (surgery, radiation, or both), and 5-year relative survival rates.
There were 4070 cases of uveal melanoma representing 3.1% of all recorded cases of melanoma. The majority of cases (98.3%) were reported by hospital inpatient/outpatient clinics. Histopathologic confirmation was available in 2804 cases (72.1% for all years). The mean age-adjusted incidence of uveal melanoma in the United States was 5.1 per million (95% CI, 4.8-5.3). The majority of cases (97.8%) occurred in the white population. There was a statistically significant variation of age-adjusted incidence between sexes (male = 5.8, 95% CI, 5.5-6.2; and female = 4.4, 95% CI, 4.2-4.7). A decreasing trend was observed in patients treated with surgery alone (93.8% for 1973-1975 vs. 28.3% for 2006-2008), whereas a corresponding increase was seen in those treated with radiation (1.8% for 1973-1975 vs. 62.5% for 2006-2008). No change in the 5-year relative survival rate (81.6%) was observed from 1973 to 2008.
The age-adjusted incidence of uveal melanoma (5.1 per million) has remained unchanged from 1973 to 2008. Despite a shift toward more conservative treatments, survival has not improved during this time period.
在 1973 年至 2008 年的 36 年间,通过对美国现有的数据库进行系统性回顾,确定原发性葡萄膜黑色素瘤的发病率、治疗和生存趋势。
对现有数据库的系统回顾。
美国监测、流行病学和最终结果(SEER)计划数据库中,1973 年至 2008 年共 4070 例原发性葡萄膜黑色素瘤患者(国际肿瘤疾病分类 [ICD-O-2] 代码 C69.3[脉络膜]、C69.4[睫状体和虹膜]和 C69.2[视网膜])。
使用卡方检验和 95%置信区间(CI)确定年龄调整发病率、治疗和 5 年相对生存率的趋势的显著性。
年龄调整发病率、治疗形式(手术、放疗或两者结合)和 5 年相对生存率。
共 4070 例葡萄膜黑色素瘤病例,占所有黑色素瘤病例的 3.1%。大多数病例(98.3%)是由医院门诊/住院诊所报告的。2804 例(所有年份的 72.1%)有组织病理学证实。美国葡萄膜黑色素瘤的平均年龄调整发病率为 5.1/100 万(95%CI,5.8-5.3)。大多数病例(97.8%)发生在白人中。男性和女性之间的年龄调整发病率存在统计学显著差异(男性=5.8,95%CI,5.5-6.2;女性=4.4,95%CI,4.2-4.7)。仅接受手术治疗的患者比例呈下降趋势(1973-1975 年为 93.8%,2006-2008 年为 28.3%),而接受放疗的患者比例则相应增加(1973-1975 年为 1.8%,2006-2008 年为 62.5%)。1973 年至 2008 年间,5 年相对生存率(81.6%)无变化。
从 1973 年到 2008 年,葡萄膜黑色素瘤的年龄调整发病率(5.1/100 万)保持不变。尽管治疗方法向更保守的方法转变,但在此期间,生存率并未提高。