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错配修复缺陷作为黏液性结直肠癌的一个预后因素

Mismatch repair deficiency as a prognostic factor in mucinous colorectal cancer.

作者信息

Andrici Juliana, Farzin Mahtab, Sioson Loretta, Clarkson Adele, Watson Nicole, Toon Christopher W, Gill Anthony J

机构信息

Cancer Diagnosis and Pathology Research Group, Kolling Institute of Medical Research, St Leonards, NSW, Australia.

Sydney Medical School, University of Sydney, Sydney, NSW, Australia.

出版信息

Mod Pathol. 2016 Mar;29(3):266-74. doi: 10.1038/modpathol.2015.159. Epub 2016 Jan 15.

Abstract

There is some uncertainty about pathological grading of mucinous colorectal adenocarcinoma, defined as colorectal cancer demonstrating at least 50% mucinous differentiation. Under the WHO 2000 classification mucinous colorectal cancer was considered high grade. However under the current WHO 2010 classification microsatellite unstable/mismatch repair-deficient (MSI/MMRd) mucinous colorectal cancer is considered low grade, whereas microsatellite stable/mismatch repair proficient (MSS/MMRp) tumours are high grade. However there is little empirical evidence for this approach. We therefore compared the long term survival of patients with MSI/MMRd vs MSS/MMRp mucinous colorectal cancer in a large unselected cohort of patients undergoing surgery at our institution from 1998 to 2011. There were 2608 patients in the cohort, of which 264 (10.1%) were mucinous. 95 (36%) of the mucinous tumours were microsatellite unstable. The all-cause 5-year survival of mucinous MSI/MMRd colorectal cancer was similar to that of non-mucinous low-grade colorectal cancer (73 vs 67%, P=0.368), and significantly better than that of both non-mucinous high-grade (73 vs 53%, P<0.001) and mucinous MSS/MMRp colorectal cancer (73 vs 57%, P=0.023). The 5-year survival of mucinous MSS/MMRp colorectal cancer was slightly better than that of non-mucinous high-grade patients (57 vs 53%, P=0.027), but significantly worse than that of non-mucinous low-grade colorectal cancer (57 vs 67%, P=0.018). In multivariate Cox regression analysis, conventional histological grade based on glandular differentiation maintained prognostic significance (P=0.003) whereas MSI/MMRd status just failed to be statistically significant (P=0.062). Our findings support the WHO 2010 approach that as a group mucinous MSS/MMRp colorectal cancers are biologically aggressive. However, grading based exclusively on MSI/MMR status may be overly simplistic as conventional grading based on the degree of glandular differentiation still holds greater prognostic significance in multivariate analysis.

摘要

黏液性结直肠癌的病理分级存在一定不确定性,黏液性结直肠癌定义为黏液分化至少达50%的结直肠癌。在世界卫生组织(WHO)2000年分类中,黏液性结直肠癌被视为高级别。然而,在当前WHO 2010分类中,微卫星不稳定/错配修复缺陷(MSI/MMRd)的黏液性结直肠癌被视为低级别,而微卫星稳定/错配修复 proficient(MSS/MMRp)肿瘤则为高级别。然而,这种方法几乎没有实证依据。因此,我们比较了1998年至2011年在我们机构接受手术的大量未选择队列中,MSI/MMRd与MSS/MMRp黏液性结直肠癌患者的长期生存率。该队列中有2608名患者,其中264名(10.1%)为黏液性。95例(36%)黏液性肿瘤微卫星不稳定。黏液性MSI/MMRd结直肠癌的全因5年生存率与非黏液性低级别结直肠癌相似(73%对67%,P = 0.368),且显著优于非黏液性高级别(73%对53%,P < 0.001)和黏液性MSS/MMRp结直肠癌(73%对57%,P = 0.023)。黏液性MSS/MMRp结直肠癌的5年生存率略优于非黏液性高级别患者(57%对53%,P = 0.027),但显著低于非黏液性低级别结直肠癌(57%对67%,P = 0.018)。在多变量Cox回归分析中,基于腺管分化的传统组织学分级保持了预后意义(P = 0.003),而MSI/MMRd状态仅未达到统计学显著性(P = 0.062)。我们的研究结果支持WHO 2010的方法,即作为一个群体,黏液性MSS/MMRp结直肠癌具有生物学侵袭性。然而,仅基于MSI/MMR状态进行分级可能过于简单,因为在多变量分析中,基于腺管分化程度的传统分级仍具有更大的预后意义。

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