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A machine learning–based transcriptomic signature for predicting tumor recurrence after curative resection in T1 colorectal cancer: a retrospective multicenter cohort study (The Tw1CE trial)

医学 转录组 肿瘤科 内科学 回顾性队列研究 切除术 生物标志物 放射科 结直肠癌 队列研究 总体生存率 队列 外科切除术 多中心研究 基因签名 试验预测值 分类器(UML) 外科
作者
Takayuki Noma,Karmele Sáez de Gordoa,M. Daca-Alvarez,Katsuki Miyazaki,Yuma Wada,Alessandro Mannucci,Takumi Onoyama,Mitsuo Shimada,Míriam Cuatrecasas,Luis Bujanda,Maria Pellisé,Ajay Goel
出处
期刊:International Journal of Surgery [Wolters Kluwer]
卷期号:112 (4): 9039-9051 被引量:1
标识
DOI:10.1097/js9.0000000000004690
摘要

BACKGROUND: T1 colorectal cancer (T1 CRC) is increasingly treated with curative-intent endoscopic resection, but tumor recurrence remains a critical factor influencing patient prognosis. However there is no validated biomarker exists to reliably predict post-resection recurrence, limiting risk-adapted follow-up and adjuvant therapy decisions. MATERIALS AND METHODS: In this multicenter retrospective cohort study across academic centers in Spain, 138 patients with T1 CRC (2023-2025; ClinicalTrials.gov NCT06314971) were enrolled. From FFPE endoscopic specimens, expression of five mRNAs and two miRNAs was quantified by RT-qPCR, and an XGBoost-based transcriptomic panel was developed. Patients were assigned to training and independent testing cohorts by treatment type. The primary outcome was 3-year recurrence-free survival (RFS); secondary outcomes included 5-year RFS and overall survival (OS). RESULTS: The transcriptomic panel demonstrated high predictive performance in both the training (AUROC = 91.7%) and testing (AUROC = 88.2%) cohorts. Patients classified as high-risk by the panel exhibited significantly worse RFS and OS compared with those classified as low-risk (log-rank P < 0.001). Furthermore, integrating lymphatic invasion with the transcriptomic panel into a combined risk stratification model further improved predictive accuracy (AUROC = 94.6%), and decision curve analysis confirmed its superior clinical utility compared to conventional criteria. CONCLUSION: This study established a validated machine learning-based transcriptomic classifier derived from endoscopic resection specimens that accurately predicts tumor recurrence in patients with T1 CRC. Our findings highlight the potential of this biomarker panel to enable risk-adapted surveillance strategies and guide decisions regarding additional therapy after curative resection.
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