Department of Pathology, Institut Universitaire du Cancer-Oncopole de Toulouse, Centre Hospitalier Universitaire (CHU), Toulouse, France.
Oncogenesis of Sarcomas, INSERM UMR1037, Cancer Research Centre of Toulouse, Toulouse, France.
Mod Pathol. 2022 Dec;35(12):2002-2010. doi: 10.1038/s41379-022-01166-9. Epub 2022 Oct 6.
The outcome of stage II-III colorectal cancer (CRC) is highly variable and therapeutic choice is currently based on TNM staging with a few additional biomarkers. However, studies show that some stage III patients have a better prognosis than some stage II patients. A promising consensus molecular (CMS) classification with prognostic relevance has been developed, but it is not used in daily practice. Our team developed CINSARC, a 67-gene expression prognostic signature, whose prognostic value has been demonstrated in many cancer types. It is applicable to formalin-fixed, paraffin-embedded (FFPE) blocks using NanoString® technology. We investigated whether it could predict outcome in stage II-III CRC. We established the CINSARC classification on the TCGA retrospective cohort comprising 297 stage II-III CRC patients using RNA sequencing and on a second independent cohort comprising 169 cases using NanoString® technology. We compared its recurrence-free and overall survival prognostic value with TNM staging and CMS classification. In the TCGA cohort, we showed that CINSARC significantly splits the population of stage II-III CRC into two groups with different progression-free interval (P = 1.68 × 10; HR = 1.87 [1.11-3.16]) and overall survival (P = 3.73 × 10; HR = 2.45 [1.31-4.59]) and is a strong prognostic factor in multivariate analysis, outperforming TNM staging and CMS classification. We validated these results in the second cohort by applying CINSARC on FFPE samples with Nanostring® technology. CINSARC is a ready-to-use tool with a robust independent prognostic value in stage II-III CRC.
Ⅱ-Ⅲ期结直肠癌(CRC)的结局差异很大,目前的治疗选择基于 TNM 分期,少数情况下还会加入一些额外的生物标志物。然而,研究表明,一些Ⅲ期患者的预后比一些Ⅱ期患者要好。目前已经开发出一种具有预后相关性的有前途的共识分子(CMS)分类,但尚未在日常实践中使用。我们的团队开发了 CINSARC,这是一种 67 个基因表达的预后标志,其预后价值已在多种癌症类型中得到证实。它适用于使用 NanoString®技术的福尔马林固定、石蜡包埋(FFPE)块。我们研究了它是否可以预测Ⅱ-Ⅲ期 CRC 的结局。我们使用 RNA 测序在包含 297 例Ⅱ-Ⅲ期 CRC 患者的 TCGA 回顾性队列中建立了 CINSARC 分类,并使用 NanoString®技术在第二个独立队列中建立了 169 例患者的分类。我们比较了其与 TNM 分期和 CMS 分类的无复发生存和总生存预后价值。在 TCGA 队列中,我们表明 CINSARC 显著地将Ⅱ-Ⅲ期 CRC 人群分为两组,两组的无进展间隔(P=1.68×10;HR=1.87[1.11-3.16])和总生存期(P=3.73×10;HR=2.45[1.31-4.59])差异显著,并且是多变量分析中的一个强有力的预后因素,优于 TNM 分期和 CMS 分类。我们通过使用 NanoString®技术在 FFPE 样本上应用 CINSARC,在第二个队列中验证了这些结果。CINSARC 是一种现成的工具,在Ⅱ-Ⅲ期 CRC 中具有稳健的独立预后价值。