Des-γ-羧基凝血酶原在肝癌术后复发风险评价中的应用。

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Communications medicine Pub Date : 2025-03-06 DOI:10.1038/s43856-025-00784-z
Xinting Pan, Yang Zhou, Zhenli Li, Pengfei Guo, Jianyang Zeng, Xiuqing Dong, En Hu, Liman Qiu, Zhixiong Cai, Geng Chen, Xiaolong Liu
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引用次数: 0

摘要

背景:虽然Des-γ-羧基凝血酶原在肝癌诊断中的价值已被广泛认可,但Des-γ-羧基凝血酶原是否或如何用于复发评估仍未被广泛探索。方法:我们进行了多中心回顾性分析,包括探索队列(1074例患者,5133个Des-γ-羧基凝血酶原测量)和验证队列(263例患者,612个Des-γ-羧基凝血酶原测量),以探讨Des-γ-羧基凝血酶原是否可以评估患者的预后。我们引入Des-γ-羧基凝血酶原动态速率作为Des-γ-羧基凝血酶原动态变化的归一化定量测量。将Des-γ-羧基凝血酶原动态率进一步应用于高危肝硬化患者队列(PreCar队列,542例肝硬化患者,2023例Des-γ-羧基凝血酶原测量)。结果:我们发现在探索队列中,术后Des-γ-羧基凝血酶原降低,使得诊断中的Des-γ-羧基凝血酶原阈值不适合预后,而Des-γ-羧基凝血酶原动态率与复发风险显著相关。根据Des-γ-羧基凝血酶原动态率和终浓度对患者进行分类,两项检测均阴性的患者中位无复发生存期最佳,两项检测均阳性的患者中位无复发生存期最差。持续呈阳性状态的患者的中位无复发生存期明显低于那些状态转为阴性的患者。这些发现在验证队列中得到了验证。此外,PreCar队列中的Des-γ-羧基凝血酶原动态率可以确定28%的肝硬化患者进展为肝细胞癌。结论:本研究结果进一步拓展了肝细胞癌诊断生物标志物Des-γ-羧基凝血酶原的临床应用,提出了一种定量测量Des-γ-羧基凝血酶原动态监测肝细胞癌复发的方法。这种测量不仅局限于预后,而且可以提高早期肝细胞癌筛查的敏感性。
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Des-γ-carboxy Prothrombin in hepatocellular carcinoma post-operative recurrence risk evaluation.

Background: While the value of Des-γ-carboxy prothrombin in hepatocellular carcinoma diagnosis has been widely acknowledged, whether or how Des-γ-carboxy prothrombin could be used in recurrence evaluation remains largely unexplored.

Methods: We performed a multicenter retrospective analysis including an Exploration Cohort (1074 patients, 5133 Des-γ-carboxy prothrombin measurements) and a Validation Cohort (263 patients, 612 Des-γ-carboxy prothrombin measurements) to investigate whether Des-γ-carboxy prothrombin could evaluate patients' prognosis. We introduced the Des-γ-carboxy prothrombin dynamic rate as a normalized quantitative measurement of Des-γ-carboxy prothrombin dynamic change. Des-γ-carboxy prothrombin dynamic rates were further applied in a high-risk liver cirrhosis patient cohort (PreCar Cohort, 542 liver cirrhosis patients, 2023 Des-γ-carboxy prothrombin measurements).

Results: Here, we show a post-operative decrease of Des-γ-carboxy prothrombin in the Exploration Cohort, making the Des-γ-carboxy prothrombin threshold in diagnosis unsuitable for prognosis, while Des-γ-carboxy prothrombin dynamic rates significantly associate with recurrence risk. Categorizing patients based on Des-γ-carboxy prothrombin dynamic rates and final concentrations shows that patients negative for both exhibit the best median recurrence-free survival and patients positive for both show the worst median recurrence-free survival. Patients with consistently positive status have a significantly lower median recurrence-free survival compared to those whose status reverted to negative. These findings are validated in the Validation Cohort. Furthermore, the Des-γ-carboxy prothrombin dynamic rates in the PreCar Cohort can identify an additional 28% of cirrhosis patients progressing to hepatocellular carcinoma.

Conclusions: These results expand on the clinical utilization of the hepatocellular carcinoma diagnosis biomarker, Des-γ-carboxy prothrombin, by proposing a quantification measurement of Des-γ-carboxy prothrombin dynamics to monitor hepatocellular carcinoma recurrence. This measurement is not limited in prognosis but can also improve the sensitivity of early hepatocellular carcinoma screening.

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