Evaluation of MRI characterisation of histopathologically matched lymph nodes and other mesorectal nodal structures in rectal cancer.

IF 4.7 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
European Radiology Pub Date : 2025-07-01 Epub Date: 2025-01-21 DOI:10.1007/s00330-025-11361-2
Miriam Kheira Rutegård, Malin Båtsman, Lennart Blomqvist, Martin Rutegård, Jan Axelsson, Wendy Wu, Ingrid Ljuslinder, Jörgen Rutegård, Richard Palmqvist, Fredrik Brännström, Katrine Riklund
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引用次数: 0

Abstract

Purpose: To evaluate current MRI-based criteria for malignancy in mesorectal nodal structures in rectal cancer.

Method: Mesorectal nodal structures identified on baseline MRI as lymph nodes were anatomically compared to their corresponding structures histopathologically, reported as lymph nodes, tumour deposits or extramural venous invasion. All anatomically matched nodal structures from patients with primary surgery and all malignant nodal structures from patients with neoadjuvant treatment were included. Mixed-effects logistic regression models were used to evaluate the morphological criteria irregular margin, round shape, heterogeneous signal and nodal size, as well as the combined 2016 European Society of Gastrointestinal and Abdominal Radiology (ESGAR) consensus criteria, with histopathological nodal status as the gold standard.

Results: In total, 458 matched nodal structures were included from 46 patients (mean age, 67.7 years ± 1.5 [SD], 27 men), of which 19 received neoadjuvant treatment. The strongest associations in the univariable model were found for short-axis diameter ≥ 5 mm (OR 21.43; 95% CI: 4.13-111.29, p < 0.001) and heterogeneous signal (OR 9.02; 95% CI: 1.33-61.08, p = 0.024). Only size remained significant in multivariable analysis (OR 12.32; 95% CI: 2.03-74.57, p = 0.006). When applying the ESGAR consensus criteria to create a binary classification of nodal status, the OR of malignant outcome for nodes with positive ESGAR was 8.23 (95% CI: 2.15-31.50, p = 0.002), with corresponding sensitivity and specificity of 54% and 85%, respectively.

Conclusion: The results confirm the role of morphological and size criteria in predicting lymph node metastases. However, the current criteria might not be accurate enough for nodal staging.

Key points: Question Pretreatment lymph node staging in rectal cancer is challenging, and the ESGAR consensus criteria are not fully validated. Findings Although the ESGAR criteria correlated with malignant outcomes, diagnostic performance in terms of particular sensitivity, but also specificity, was not high. Clinical relevance Accurate nodal staging in rectal cancer is crucial for individual treatment planning. However, this validation of the current ESGAR consensus criteria suggests that these should be used with caution.

直肠癌组织病理学匹配的淋巴结和其他肠系膜结结构的MRI特征评价。
目的:评价当前基于mri的直肠癌肠系膜结结构恶性肿瘤的诊断标准。方法:在基线MRI上识别为淋巴结的肠系膜结结构在解剖学上与其相应的组织病理学结构进行比较,报告为淋巴结,肿瘤沉积物或外静脉侵入。所有初次手术患者解剖匹配的淋巴结结构和所有新辅助治疗患者的恶性淋巴结结构被纳入研究。采用混合效应logistic回归模型评估边缘不规则、形状圆形、信号异质性和淋巴结大小的形态学标准,以及2016年欧洲胃肠和腹部放射学会(ESGAR)联合共识标准,以组织病理学淋巴结状态为金标准。结果:46例患者(平均年龄67.7岁±1.5 [SD],男性27例)共纳入匹配淋巴结458个,其中19例接受了新辅助治疗。在单变量模型中,短轴直径≥5 mm的相关性最强(OR 21.43;95% CI: 4.13-111.29, p结论:结果证实了形态学和大小标准在预测淋巴结转移中的作用。然而,目前的标准对于淋巴结分期可能不够准确。直肠癌淋巴结分期的预处理具有挑战性,ESGAR共识标准尚未得到充分验证。尽管ESGAR标准与恶性预后相关,但在特定敏感性和特异性方面的诊断性能并不高。准确的直肠癌淋巴结分期对个体化治疗计划至关重要。然而,对当前ESGAR共识标准的验证表明,这些标准应该谨慎使用。
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来源期刊
European Radiology
European Radiology 医学-核医学
CiteScore
11.60
自引率
8.50%
发文量
874
审稿时长
2-4 weeks
期刊介绍: European Radiology (ER) continuously updates scientific knowledge in radiology by publication of strong original articles and state-of-the-art reviews written by leading radiologists. A well balanced combination of review articles, original papers, short communications from European radiological congresses and information on society matters makes ER an indispensable source for current information in this field. This is the Journal of the European Society of Radiology, and the official journal of a number of societies. From 2004-2008 supplements to European Radiology were published under its companion, European Radiology Supplements, ISSN 1613-3749.
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