Aaberg Thomas M, Covington Kyle R, Tsai Tony, Shildkrot Yevgeniy, Plasseraud Kristen M, Alsina Katherina M, Oelschlager Kristen M, Monzon Federico A
Retina Specialists of Michigan, Michigan State University, Grand Rapids, Michigan, USA.
Castle Biosciences, Inc., Friendswood, Texas, USA.
Ocul Oncol Pathol. 2020 Oct;6(5):360-367. doi: 10.1159/000508382. Epub 2020 Jul 6.
The prognostic 15-gene expression profile (15-GEP) test for uveal melanoma (UM) predicts metastatic risk based on primary tumor biology. Here we report outcomes from a prospective registry of 15-GEP-tested patients, and a meta-analysis with published cohorts.
Management and 5-year clinical outcomes following 15-GEP testing were evaluated.
Eighty-nine patients with 15-GEP results were prospectively enrolled at four centers. Physician-recommended management plans were collected, and clinical outcomes tracked every 6 months.
Eighty percent of Class 1 (low-risk) patients underwent low-intensity management; all Class 2 (high-risk) patients underwent high-intensity management ( < 0.0001). Median follow-up for event-free patients was 4.9 years. Five Class 1 (10%) and 23 Class 2 (58%) tumors metastasized ( < 0.0001). Five-year Class 1 and 2 metastasis-free survival rates were 90% (81-100%) and 41% (27-62%; < 0.0001), and melanoma-specific survival rates were 94% (87-100%) and 63% (49-82%; = 0.0007). Class 2 was the only independent predictor of metastasis and was associated with increased risk for metastasis and mortality by meta-analysis.
UM patient management is guided by 15-GEP testing. Class 2 patients were managed more intensely, in accordance with an observed metastatic rate of >50%; Class 1 patients were safely spared intensive surveillance, resulting in appropriate utilization of healthcare resources.
葡萄膜黑色素瘤(UM)的预后15基因表达谱(15-GEP)检测基于原发性肿瘤生物学特征预测转移风险。在此,我们报告了对接受15-GEP检测患者的前瞻性登记研究结果,以及与已发表队列的荟萃分析结果。
评估15-GEP检测后的管理及5年临床结局。
在四个中心前瞻性纳入了89例有15-GEP检测结果的患者。收集医生推荐的管理计划,并每6个月跟踪临床结局。
80%的1类(低风险)患者接受了低强度管理;所有2类(高风险)患者均接受了高强度管理(<0.0001)。无事件患者的中位随访时间为4.9年。5例1类(10%)和23例2类(58%)肿瘤发生转移(<0.0001)。1类和2类的5年无转移生存率分别为90%(81-100%)和41%(27-62%;<0.0001),黑色素瘤特异性生存率分别为94%(87-100%)和63%(49-82%;P = 0.0007)。2类是转移的唯一独立预测因素,荟萃分析显示其与转移风险和死亡率增加相关。
UM患者的管理以15-GEP检测为指导。2类患者接受了更强化的管理,这与观察到的>50%的转移率一致;1类患者可安全地免于强化监测,从而实现医疗资源的合理利用。