Sarah Cannon Research Institute and Tennessee Oncology, PLLC, Nashville, TN 37203, USA.
J Natl Cancer Inst. 2013 Jun 5;105(11):782-90. doi: 10.1093/jnci/djt099. Epub 2013 May 2.
BACKGROUND: Molecular tumor profiling (MTP) is a potentially powerful diagnostic tool for identifying the tissue of origin in patients with cancer of unknown primary (CUP). However, validation of the accuracy and clinical value of MTP has been difficult because the anatomic primary site in most patients is never identified. METHODS: From March 2008 through January 2010, clinicopathologic data from 171 CUP patients who had MTP (CancerTYPE ID; bioTheranostics, Inc, San Diego, CA) performed on archived material were evaluated. The accuracy of MTP diagnoses was evaluated by comparison with (1) latent primary tumor sites found months/years later; (2) initial single diagnoses by immunohistochemistry (IHC); and (3) additional directed IHC and/or clinicopathologic findings evaluated after MTP diagnoses. RESULTS: A single MTP diagnosis was made in 144 of 149 patients with adequate tumor specimens. Eighteen of 24 patients with latent primaries discovered months to years later had correct diagnoses by MTP (75%), and these diagnoses compared favorably with IHC. Single IHC diagnoses matched MTP diagnoses in 40 of 52 patients (77%). IHC predictions of 2 or more possible primaries compared poorly with MTP diagnoses. However, additional targeted IHC and clinical/histologic evaluation supported the MTP diagnosis in 26 of 35 patients (74%). Clinical features were usually consistent with MTP diagnoses (70%). CONCLUSIONS: The diagnostic accuracy of this MTP assay was supported by a high level of agreement with identified latent primaries (75%), single IHC diagnoses (77%), and additional directed IHC and/or clinical/histologic findings (74%) prompted by the MTP diagnoses. MTP complements standard pathologic evaluation in determining the tissue of origin in patients with CUP, particularly when IHC is inconclusive.
背景:分子肿瘤分析(MTP)是一种潜在的强大诊断工具,可用于确定癌症未知原发性(CUP)患者的组织来源。然而,由于大多数患者的解剖原发性部位从未确定,因此验证 MTP 的准确性和临床价值一直很困难。
方法:从 2008 年 3 月至 2010 年 1 月,对 171 名接受 MTP(CancerTYPE ID;生物治疗诊断公司,圣地亚哥,加利福尼亚州)检测的 CUP 患者的临床病理数据进行了评估。通过与(1)数月/数年后发现的潜在原发性肿瘤部位;(2)初次免疫组织化学(IHC)单一诊断;(3)MTP 诊断后评估的额外定向 IHC 和/或临床病理发现进行比较,评估 MTP 诊断的准确性。
结果:在 149 名有足够肿瘤标本的患者中,144 名患者进行了单一 MTP 诊断。在 24 名数月至数年后发现潜在原发性的患者中,18 名(75%)的患者 MTP 诊断正确,这些诊断与 IHC 结果相当。在 52 名患者中,40 名(77%)的患者的 IHC 诊断与 MTP 诊断相匹配。IHC 预测 2 个或更多可能的原发性与 MTP 诊断相比效果不佳。然而,26 名(74%)患者的额外靶向 IHC 和临床/组织学评估支持 MTP 诊断。临床特征通常与 MTP 诊断相符(70%)。
结论:MTP 检测的诊断准确性得到了高度认可,与确定的潜在原发性(75%)、单一 IHC 诊断(77%)以及 MTP 诊断后提示的额外定向 IHC 和/或临床/组织学发现(74%)高度一致。MTP 补充了标准病理评估,有助于确定 CUP 患者的组织来源,尤其是在 IHC 结果不确定时。
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