Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH 44195, United States.
Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH 44195, United States.
Semin Diagn Pathol. 2021 Nov;38(6):193-198. doi: 10.1053/j.semdp.2020.12.001. Epub 2020 Dec 4.
Cancer of unknown primary (CUP) refers to metastatic tumors for which the primary tumor of origin cannot be determined at the time of diagnosis, despite extensive clinicopathologic investigations. Molecular profiling is increasingly able to predict a probable primary tumor type for CUP when clinicopathologic workup is inconclusive. Numerous studies have explored the use of various molecular profiling techniques for identification of site/tissue of origin of CUP. These techniques include gene expression profiling utilizing microarray, reverse transcriptase polymerase chain reaction, RNA-sequencing, somatic gene mutation profiling with next-generation DNA sequencing, and epigenomics including DNA methylation profiling. Despite the generally poor prognosis of CUP, a minority of patients can expect to benefit from targeted therapy despite being agnostic to the tissue of origin. Studies have explored the use of various molecular profiling techniques to predict prognostic and therapeutic biomarkers, with the goal of improving outcome for patients with CUP. However, discordant results between non-randomized and randomized clinical trials in evaluating tumor-type specific therapies raise uncertainties of the benefits of molecularly-predicted tissue of origin-based treatment in routine clinical use. Nevertheless, the current overall trend is in favor of using molecular tools to refine the diagnosis and clinical management of patients with CUP. More large-cohort, randomized prospective studies are needed to assess and validate the utility and feasibility of molecular profiling to uncover potentially targetable genetic alterations. These efforts will also yield further biological insights into the biology and pathogenesis of CUP (Graphical Abstract).
原发灶不明的癌症(CUP)是指转移瘤,尽管进行了广泛的临床病理检查,但在诊断时仍无法确定其原发肿瘤的起源。当临床病理检查结果不确定时,分子谱分析越来越能够预测 CUP 的可能原发肿瘤类型。许多研究都探讨了各种分子谱分析技术在确定 CUP 的起源部位/组织中的应用。这些技术包括利用微阵列进行基因表达谱分析、逆转录聚合酶链反应、RNA 测序、下一代 DNA 测序进行体细胞基因突变谱分析,以及包括 DNA 甲基化谱分析在内的表观基因组学。尽管 CUP 的总体预后较差,但少数患者即使对起源组织未知,也可能受益于靶向治疗。研究已经探讨了使用各种分子谱分析技术来预测预后和治疗生物标志物,以期改善 CUP 患者的预后。然而,在评估肿瘤特异性治疗的非随机和随机临床试验之间存在不一致的结果,这使得基于分子预测的起源组织治疗在常规临床应用中的获益存在不确定性。尽管如此,目前的总体趋势是倾向于使用分子工具来完善 CUP 患者的诊断和临床管理。需要更多的大样本、随机前瞻性研究来评估和验证分子谱分析在揭示潜在可靶向遗传改变方面的效用和可行性。这些努力还将进一步深入了解 CUP 的生物学和发病机制(示意图)。