Bagger Mette, Andersen Morten T, Andersen Klaus K, Heegaard Steffen, Andersen Mette K, Kiilgaard Jens F
Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark Department of Ophthalmology, Copenhagen University Hospital, Glostrup, Denmark.
Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Invest Ophthalmol Vis Sci. 2014 Dec 23;56(1):438-44. doi: 10.1167/iovs.14-15571.
To evaluate the prognostic effect of a combination of American Joint Committee on Cancer (AJCC) staging (7th edition) and genetic status in patients with posterior uveal melanoma.
A consecutive cohort of 153 patients with posterior uveal melanoma treated at Copenhagen University Hospital from January 1, 2009 through December 31, 2012 was followed until October 2014. Survival, AJCC stage, and cytogenetic data were registered. The AJCC stage was available for all patients, and cytogenetic information for chromosomes 3 and 8 was available for 139 patients. The individual and joint prognostic effects of AJCC staging and cytogenetic changes were evaluated by cumulative incidence curves and Cox proportional hazard models.
An overall 5-year survival rate of 62% (95% confidence interval [CI]: 0.50-0.73) was observed. A normal genetic status of chromosomes 3 and 8, as found in 42 patients (30%), minimized the additional prognostic effect of AJCC staging. The frequency of tumors with normal genetic status decreased with increasing AJCC stage. Both AJCC stage III (hazard ratio [HR]: 11.0, 95% CI: 1.4-85.6) and abnormal copy number of chromosomes 3 (HR: 6.3, 95% CI: 1.4-28.3) and 8 (HR: 2.8, 95% CI: 1.03-7.8) were identified as significant predictors of a poor prognosis in the multivariate Cox regression analysis.
Identification of a normal genetic status of chromosomes 3 and 8 minimized the prognostic effect of AJCC staging, while a combination of genetic status and AJCC staging provided the most accurate prediction of survival in patients with an abnormal chromosomal status.
评估美国癌症联合委员会(AJCC)分期(第7版)与基因状态相结合对后葡萄膜黑色素瘤患者的预后影响。
对2009年1月1日至2012年12月31日在哥本哈根大学医院接受治疗的153例后葡萄膜黑色素瘤患者的连续队列进行随访,直至2014年10月。记录生存情况、AJCC分期和细胞遗传学数据。所有患者均有AJCC分期数据,139例患者有染色体3和8的细胞遗传学信息。通过累积发病率曲线和Cox比例风险模型评估AJCC分期和细胞遗传学变化的个体及联合预后影响。
观察到总体5年生存率为62%(95%置信区间[CI]:0.50 - 0.73)。42例患者(30%)的染色体3和8基因状态正常,这使AJCC分期的额外预后影响最小化。基因状态正常的肿瘤频率随AJCC分期增加而降低。在多变量Cox回归分析中,AJCC III期(风险比[HR]:11.0,95% CI:1.4 - 85.6)以及染色体3(HR:6.3,95% CI:1.4 - 28.3)和8(HR:2.8,95% CI:1.03 - 7.8)的拷贝数异常均被确定为预后不良的显著预测因素。
确定染色体3和8的基因状态正常可使AJCC分期的预后影响最小化,而基因状态与AJCC分期相结合可对染色体状态异常的患者生存情况提供最准确的预测。