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Targeted Plasma Metabolic Profiles and Risk of Recurrence in Stage II and III Colorectal Cancer Patients: Results from an International Cohort Consortium

机译:有针对性的血浆代谢谱和阶段II和III结直肠癌患者的复发风险:国际队列财团的结果

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摘要

The identification of patients at high-risk for colorectal cancer (CRC) recurrence remains an unmet clinical need. The aim of this study was to investigate associations of metabolites with risk of recurrence in stage II/III CRC patients. A targeted metabolomics assay (128 metabolites measured) was performed on pre-surgery collected EDTA plasma samples from n = 440 newly diagnosed stage II/III CRC patients. Patients have been recruited from four prospective cohort studies as part of an international consortium: Metabolomic profiles throughout the continuum of CRC (MetaboCCC). Cox proportional hazard models were computed to investigate associations of metabolites with recurrence, adjusted for age, sex, tumor stage, tumor site, body mass index, and cohort; false discovery rate (FDR) was used to account for multiple testing. Sixty-nine patients (15%) had a recurrence after a median follow-up time of 20 months. We identified 13 metabolites that were nominally associated with a reduced risk of recurrence. None of the associations were statistically significant after controlling for multiple testing. Pathway topology analyses did not reveal statistically significant associations between recurrence and alterations in metabolic pathways (e.g., sphingolipid metabolism p = 0.04; pFDR = 1.00). To conclude, we did not observe statistically significant associations between metabolites and CRC recurrence using a well-established metabolomics assay. The observed results require follow-up in larger studies.
机译:在高风险癌症(CRC)复发中鉴定患者仍然是未核心的临床需求。本研究的目的是调查代谢物与阶段II / III阶段患者复发风险的关联。对术前手术预接种的EDTA等离子体样品进行了靶向的代谢物测定(测量了128个代谢物),来自N = 440阶段II / III CRC患者。患者已从四个潜在队列研究中招募了作为国际财团的一部分:在CRC的连续内的代谢组分(Metaboccc)。 Cox比例危害模型被计算为调查代谢物与复发,调整年龄,性别,肿瘤阶段,肿瘤部位,体重指数和队列的核心;假发现速率(FDR)用于考虑多次测试。在20个月的中位后续时间后,六十九名患者(15%)发生复发。我们确定了13个代谢物,其名义上与减少的复发风险降低。在控制多次测试后,没有关联在统计学意义。途径拓扑分析未透露代谢途径中复发和改变之间的统计上显着的关联(例如,鞘醇脂代谢P = 0.04; PFDR = 1.00)。为了得出结论,使用良好的代谢组种测定,我们没有观察到代谢物和CR​​C复发之间的统计上显着的关联。观察到的结果需要在更大的研究中进行随访。

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