Unit of Anatomic Pathology, Department of Molecular Medicine, University of Pavia, and Fondazione IRCCS San Matteo Hospital, Pavia, Italy.
Pathology Unit, Department of Surgical and Diagnostic Sciences, University Hospital and Ospedale Policlinico San Martino IRCCS, Genova, Italy.
J Crohns Colitis. 2020 Mar 13;14(3):295-302. doi: 10.1093/ecco-jcc/jjz140.
Crohn's disease-associated small bowel carcinoma is a rare event, usually reported to have a severe prognosis. However, in previous investigations we have found a minority of cases displaying a relatively favourable behaviour, thus outlining the need to improve the histopathological prediction of Crohn's disease-associated small bowel carcinoma prognosis.
As in recent studies on colorectal cancer, a substantial improvement in prognostic evaluations has been provided by the histological analysis of the tumour invasive front; we therefore systematically analysed the tumour budding and poorly differentiated clusters in the invasive front of 47 Crohn's disease-associated small bowel carcinomas collected through the Small Bowel Cancer Italian Consortium.
Both tumour budding and poorly differentiated cluster analyses proved highly effective in prognostic evaluation of Crohn's disease-associated small bowel carcinomas. In addition, they retained prognostic value when combined with two other parameters, i.e. glandular histology and stage I/II, both known to predict a relatively favourable small bowel carcinoma behaviour. In particular, association of tumour budding and poorly differentiated clusters in a combined invasive front score allowed identification of a minor subset of cancers [12/47, 25%] characterised by combined invasive front low grade coupled with a glandular histology and a low stage [I or II] and showing no cancer-related death during a median follow-up of 73.5 months.
The improved distinction of lower- from higher-grade Crohn's disease-associated small bowel carcinomas provided by invasive front analysis should be of potential help in choosing appropriate therapy for these rare and frequently ominous neoplasms.
克罗恩病相关的小肠癌是一种罕见的事件,通常报道预后严重。然而,在之前的研究中,我们发现少数病例表现出相对有利的行为,因此需要提高对克罗恩病相关小肠癌预后的组织病理学预测。
正如在最近的结直肠癌研究中,肿瘤侵袭前沿的组织学分析为预后评估提供了实质性的改进;因此,我们通过意大利小肠癌联合研究收集的 47 例克罗恩病相关小肠癌,系统地分析了肿瘤芽和侵袭前沿的低分化簇。
肿瘤芽和低分化簇分析在克罗恩病相关小肠癌的预后评估中均具有高度的有效性。此外,当与其他两个参数(即腺体组织学和 I/II 期)结合时,它们保留了预后价值,这两个参数已知可预测相对有利的小肠癌行为。特别是,肿瘤芽和低分化簇在联合侵袭前沿评分中的联合与腺体组织学和低分期(I 期或 II 期)相结合,同时伴有联合侵袭前沿低度分级的肿瘤相关簇的关联,允许确定一小部分癌症[12/47,25%],其特点是联合侵袭前沿低度分级、腺体组织学和低分期[I 期或 II 期],并且在中位随访 73.5 个月期间没有癌症相关死亡。
侵袭前沿分析提供的对克罗恩病相关小肠癌高低分级的更好区分,对于选择这些罕见且经常发生的恶性肿瘤的适当治疗可能具有潜在帮助。