Harbour J William, Chen Royce
Vice Chairman for Translational Research Professor of Ophthalmology Director, Ocular Oncology Service Bascom Palmer Eye Institute University of Miami School of Medicine.
PLoS Curr. 2013 Apr 9;5:ecurrents.eogt.af8ba80fc776c8f1ce8f5dc485d4a618. doi: 10.1371/currents.eogt.af8ba80fc776c8f1ce8f5dc485d4a618.
Uveal melanoma (UM) is the most common primary cancer of the eye and has a strong propensity for metastasis. Although there have been many recent improvements in the diagnosis and treatment of UM, and only 2-4% of patients present with detectable metastasis, up to half of patients are at risk for dying of metastatic disease. Clinicopathologic factors are not accurate enough for individualized patient care. Chromosomal alterations have been used for prognostic purposes, but the routine clinical use of these methods is limited by their susceptibility to sampling error resulting from tumor heterogeneity, limited clinical validation, lack of standardized testing platforms, and high technical failure rates. In contrast, the DecisionDx-UM gene expression profile test is a stand-alone platform which requires no other information for maximal prognostic accuracy and which circumvents many of the drawbacks of chromosomal methods through the use of a highly sensitive microfluidics, PCR-based platform that simultaneously measures the expression of 15 carefully selected genes from primary uveal melanoma samples obtained by fine needle biopsy. Low metastatic risk is reported as Class 1, and high metastatic risk as Class 2. The test allows patients to be stratified into risk categories such that high-risk patients can be offered intensive metastatic surveillance and adjuvant therapy while low-risk patients can be spared these interventions. This test is now used as part of the standard of care in many ocular oncology centers.
葡萄膜黑色素瘤(UM)是最常见的眼部原发性癌症,极易发生转移。尽管近年来UM的诊断和治疗有了许多进展,且只有2%-4%的患者出现可检测到的转移,但多达一半的患者有死于转移性疾病的风险。临床病理因素对于个体化患者护理而言不够准确。染色体改变已被用于预后评估,但这些方法在常规临床应用中受到限制,原因包括肿瘤异质性导致的采样误差、临床验证有限、缺乏标准化检测平台以及高技术失败率。相比之下,DecisionDx-UM基因表达谱检测是一个独立的平台,无需其他信息即可实现最大预后准确性,并且通过使用高度敏感的基于微流控PCR的平台,该平台可同时测量从细针穿刺活检获得的原发性葡萄膜黑色素瘤样本中15个精心挑选基因的表达,从而规避了染色体方法的许多缺点。低转移风险报告为1类,高转移风险报告为2类。该检测可将患者分层为不同风险类别,从而可以对高风险患者进行强化转移监测和辅助治疗,而低风险患者则无需这些干预措施。目前,该检测在许多眼科肿瘤中心已作为标准治疗的一部分使用。