Natoli C, Ramazzotti V, Nappi O, Giacomini P, Palmeri S, Salvatore M, Landriscina M, Zilli M, Natali P G, Tinari N, Iacobelli S
Unit of Medical Oncology, Department of Oncology and Experimental Medicine and CeSI, Fondazione 'G. D' Annunzio', University of Chieti-Pescara, 66100 Chieti, Italy.
Biochim Biophys Acta. 2011 Aug;1816(1):13-24. doi: 10.1016/j.bbcan.2011.02.002. Epub 2011 Mar 1.
An unknown primary tumor (UPT) is defined by the presence of a metastatic cancer without a known primary site of origin despite a standardized diagnostic workup. Clinically, UPTs show rapid progression and early dissemination, with signs and symptoms related to the metastatic site. The molecular bases of their biology remain largely unknown, with no evidence as to whether they represent a distinct biological entity. Immunohistochemistry remain the best diagnostic tool in term of cost-effectiveness, but the time-consuming "algorithmic process" it relies on has led to the application of new molecular techniques for the identification of the primary site of UPTs. For example, several microarray or miRNA classifications of UPTs have been used, with an accuracy in the prediction of the primary site as high as 90%. It should be noted that validating a prediction of tissue origin is challenging in these patients, since most of them will never have a primary site identified. Moreover, prospective studies to determine whether selection of treatment options based on such profiling methods actually improves patient outcome are still missing. In the last few years functional imaging (i.e. FDG-PET/CT) has gained a main role in the detection of the site of origin of UPTs and is currently recommended by the European Association of Nuclear Medicine. However, despite recent refinements in the diagnostic workup, the site of origin of UPT often remains elusive. As a consequence, treatment of patients with UPT is still empirical and inadequate.
未知原发肿瘤(UPT)的定义是,尽管进行了标准化诊断检查,但仍存在转移癌且原发起源部位不明。临床上,UPT进展迅速且早期播散,伴有与转移部位相关的体征和症状。其生物学的分子基础在很大程度上仍不清楚,尚无证据表明它们是否代表一种独特的生物学实体。就成本效益而言,免疫组织化学仍是最佳诊断工具,但它所依赖的耗时“算法过程”促使人们应用新的分子技术来识别UPT的原发部位。例如,已经使用了几种UPT的微阵列或miRNA分类方法,对原发部位的预测准确率高达90%。应当指出的是,在这些患者中验证组织起源的预测具有挑战性,因为他们中的大多数人永远无法确定原发部位。此外,确定基于此类分析方法选择治疗方案是否真的能改善患者预后的前瞻性研究仍然缺乏。在过去几年中,功能成像(即FDG-PET/CT)在检测UPT的起源部位方面发挥了主要作用,目前被欧洲核医学协会推荐使用。然而,尽管最近诊断检查有所改进,但UPT的起源部位往往仍然难以捉摸。因此,UPT患者的治疗仍然是经验性的且不充分。