Preoperative CT deep learning of tumor and visceral adipose tissue combined with postoperative pathology predicts colorectal cancer recurrence: a multicenter study.

IF 4.4 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Frontiers in Molecular Biosciences Pub Date : 2026-09-24 eCollection Date: 2026-01-01 DOI:10.3389/fmolb.2026.1937172
Pengfei Wei, Linhua Zhong, Yongming Tan, Jinhong Zhao, Yongjie Zhou
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引用次数: 0

Abstract

Introduction: To develop and externally validate a preoperative CT imaging model integrating primary tumour and visceral adipose tissue (VAT) features for predicting recurrence in colorectal cancer (CRC).

Materials and methods: This retrospective multicentre study included 1,369 patients with CRC undergoing upfront curative-intent resection, comprising a training cohort (n = 705) and two external test cohorts (n = 425 and 239). A 3D convolutional neural network extracted tumour-centred volumetric features, while an attention-based multiple instance learning branch aggregated whole-abdominal VAT slices into patient-level representations. The two CT-derived scores constituted the preoperative imaging model. A clinicopathological component was combined with the imaging scores to construct the postoperative multimodal model; robustness to variable selection was evaluated using an all-candidate ridge-penalised Cox sensitivity model.

Results: Both tumour and VAT DL scores remained independently associated with recurrence-free survival after multivariable adjustment. In external test cohorts 1 and 2, the preoperative Tumor + VAT imaging model achieved C-indices of 0.734 and 0.772, whereas the postoperative multimodal model achieved C-indices of 0.772 and 0.810 and 2-year time-dependent AUCs of 0.757 and 0.836, respectively. Training-derived tertile cut-offs from the postoperative model consistently stratified patients into low-, intermediate- and high-risk groups across all cohorts (all log-rank P < 0.001). In the two external cohorts, the clinicopathological-only model achieved C-indices of 0.709 and 0.715, compared with 0.772 and 0.810 for the postoperative multimodal model.

Conclusion: The preoperative CT model non-invasively stratified recurrence risk using tumour and whole-abdominal VAT phenotypes, while postoperative clinicopathological features further improved prognostic performance.

术前肿瘤及内脏脂肪组织CT深度学习结合术后病理预测结直肠癌复发:一项多中心研究
目的:开发并外部验证一种整合原发肿瘤和内脏脂肪组织(VAT)特征的术前CT成像模型,用于预测结直肠癌(CRC)的复发。材料和方法:这项回顾性多中心研究纳入了1369例接受前期治疗目的切除的结直肠癌患者,包括一个训练队列(n = 705)和两个外部测试队列(n = 425和239)。3D卷积神经网络提取肿瘤为中心的体积特征,而基于注意力的多实例学习分支将整个腹部VAT切片聚合为患者级表示。这两个ct评分构成了术前影像学模型。将临床病理成分与影像学评分相结合,构建术后多模态模型;使用全候选脊惩罚Cox敏感性模型评估变量选择的稳健性。结果:在多变量调整后,肿瘤和VAT DL评分仍然与无复发生存独立相关。在外部测试队列1和2中,术前肿瘤+ VAT成像模型的c指数分别为0.734和0.772,而术后多模态模型的c指数分别为0.772和0.810,2年时间依赖性auc分别为0.757和0.836。术后模型中训练衍生的五分位数截断值在所有队列中一致地将患者分为低、中、高风险组(所有log-rank P < 0.001)。在两个外部队列中,仅临床病理模型的c指数为0.709和0.715,而术后多模态模型的c指数为0.772和0.810。结论:术前CT通过肿瘤和全腹VAT表型模型无创分层复发风险,术后临床病理特征进一步改善预后表现。
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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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