Horlings Hugo M, van Laar Ryan K, Kerst Jan-Martijn, Helgason Helgi H, Wesseling Jelle, van der Hoeven Jacobus J M, Warmoes Marc O, Floore Arno, Witteveen Anke, Lahti-Domenici Jaana, Glas Annuska M, Van't Veer Laura J, de Jong Daphne
Division of Pathology, the Netherlands Cancer Institute, Amsterdam, the Netherlands.
J Clin Oncol. 2008 Sep 20;26(27):4435-41. doi: 10.1200/JCO.2007.14.6969.
Patients with adenocarcinoma of unknown primary origin (ACUP) constitute approximately 4% of all malignancies. For effective treatment of these patients, it is considered optimal to identify the primary tumor origins. Currently, the success rate of the diagnostic work-up is only 20% to 30%. Our goal was to evaluate the contribution of gene expression profiling for routine clinical practice in patients with ACUP.
Formalin-fixed, paraffin-embedded (FFPE) samples were obtained from 84 patients with a known primary adenocarcinoma and from 38 patients with ACUP. An extensive immunohistochemical panel classified 16 of the patients with ACUP, whereas 22 patients remained unclassified for their histogenetic origin. Information about staging procedures and clinical follow-up were available in all patient cases. The expression data were analyzed in relation to clinicopathologic variables and immunohistochemical results.
The gene expression-based assay classified the primary site correctly in 70 (83%) of 84 patient cases of primary and metastatic tumors of known origin, with good sensitivity for the majority of the tumor classes and relatively poor sensitivity for primary lung adenocarcinoma. Gene expression profiling identified 15 (94%) of 16 patients with initial ACUP who were classified by immunohistochemistry, and it made a valuable contribution to a potential site of origin in 14 of the 22 patients with ACUP.
The gene expression platform can classify correctly from FFPE samples the majority of tumors classes both in patients with known primary and in patients with ACUP. Therefore, gene expression profiling represents an additional analytic approach to assist with the histogenetic diagnosis of patients with ACUP.
原发灶不明的腺癌(ACUP)患者约占所有恶性肿瘤患者的4%。为有效治疗这些患者,确定原发肿瘤的起源被认为是最佳方案。目前,诊断性检查的成功率仅为20%至30%。我们的目标是评估基因表达谱分析在ACUP患者常规临床实践中的作用。
从84例已知原发性腺癌患者和38例ACUP患者中获取福尔马林固定、石蜡包埋(FFPE)样本。通过广泛的免疫组织化学检测对16例ACUP患者进行了分类,而另外22例患者的组织发生学起源仍未明确。所有患者均有分期程序和临床随访信息。对表达数据与临床病理变量及免疫组织化学结果进行了分析。
基于基因表达的检测方法在84例已知原发和转移肿瘤的患者中,正确分类了70例(83%)的原发部位,对大多数肿瘤类型具有良好的敏感性,而对原发性肺腺癌的敏感性相对较差。基因表达谱分析识别出了16例经免疫组织化学分类的初始ACUP患者中的15例(94%),并且对22例ACUP患者中的14例的潜在起源部位做出了有价值的贡献。
基因表达平台能够从FFPE样本中正确分类大多数已知原发性患者和ACUP患者的肿瘤类型。因此,基因表达谱分析是辅助ACUP患者组织发生学诊断的一种额外分析方法。