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预测肝细胞癌复发及患者术后总体生存的列线图

Nomograms for Predicting Hepatocellular Carcinoma Recurrence and Overall Postoperative Patient Survival.

作者信息

Ma Lidi, Deng Kan, Zhang Cheng, Li Haixia, Luo Yingwei, Yang Yingsi, Li Congrui, Li Xinming, Geng Zhijun, Xie Chuanmiao

机构信息

Department of Radiology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangzhou, China.

Clinical Science, Philips Healthcare, Guangzhou, China.

出版信息

Front Oncol. 2022 Feb 28;12:843589. doi: 10.3389/fonc.2022.843589. eCollection 2022.

DOI:10.3389/fonc.2022.843589
PMID:35296018
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8919774/
Abstract

BACKGROUND

Few studies have focused on the prognosis of patients with hepatocellular carcinoma (HCC) of Barcelona Clinic Liver Cancer (BCLC) stage 0‒C in terms of early recurrence and 5-years overall survival (OS). We sought to develop nomograms for predicting 5-year OS and early recurrence after curative resection of HCC, based on a clinicopathological‒radiological model. We also investigated whether different treatment methods influenced the OS of patients with early recurrence.

METHODS

Retrospective data, including clinical pathology, radiology, and follow-up data, were collected for 494 patients with HCC who underwent hepatectomy. Nomograms estimating OS and early recurrence were constructed using multivariate Cox regression analysis, based on the random survival forest (RSF) model. We evaluated the discrimination and calibration abilities of the nomograms using concordance indices (C-index), calibration curves, and Kaplan‒Meier curves. OS curves of different treatments for patients who had recurrence within 2 years after curative surgery were depicted and compared using the Kaplan-Meier method and the log-rank test.

RESULTS

Multivariate Cox regression revealed that BCLC stage, non-smooth margin, maximum tumor diameter, age, aspartate aminotransferase levels, microvascular invasion, and differentiation were prognostic factors for OS and were incorporated into the nomogram with good predictive performance in the training (C-index: 0.787) and testing cohorts (C-index: 0.711). A nomogram for recurrence-free survival was also developed based on four prognostic factors (BCLC stage, non-smooth margin, maximum tumor diameter, and microvascular invasion) with good predictive performance in the training (C-index: 0.717) and testing cohorts (C-index: 0.701). In comparison to the BCLC staging system, the C-index (training cohort: 0.787 vs. 0.678, 0.717 vs. 0.675; external cohort 2: 0.748 vs. 0.624, 0.729 vs. 0.587 respectively, for OS and RFS; external cohort1:0.716 vs. 0.627 for RFS, all p value<0.05), and model calibration curves all showed improved performance. Patients who underwent surgery after tumor recurrence had a higher reOS than those who underwent comprehensive treatments and supportive care.

CONCLUSIONS

The nomogram, based on clinical, pathological, and radiological factors, demonstrated good accuracy in estimating OS and recurrence, which can guide follow-up and treatment of individual patients. Reoperation may be the best option for patients with recurrence in good condition.

摘要

背景

很少有研究关注巴塞罗那临床肝癌(BCLC)0‒C期肝细胞癌(HCC)患者的早期复发和5年总生存期(OS)的预后情况。我们试图基于临床病理‒放射学模型开发列线图,以预测HCC根治性切除术后的5年OS和早期复发情况。我们还研究了不同治疗方法是否会影响早期复发患者的OS。

方法

收集了494例行肝切除术的HCC患者的回顾性数据,包括临床病理、放射学和随访数据。基于随机生存森林(RSF)模型,使用多变量Cox回归分析构建了估计OS和早期复发的列线图。我们使用一致性指数(C指数)、校准曲线和Kaplan‒Meier曲线评估了列线图的辨别能力和校准能力。采用Kaplan-Meier法和对数秩检验描绘并比较了根治性手术后2年内复发患者不同治疗方法的OS曲线。

结果

多变量Cox回归显示,BCLC分期、边缘不光滑、最大肿瘤直径、年龄、天冬氨酸转氨酶水平、微血管侵犯和分化程度是OS的预后因素,并被纳入列线图,在训练队列(C指数:0.787)和测试队列(C指数:0.711)中具有良好的预测性能。还基于四个预后因素(BCLC分期、边缘不光滑、最大肿瘤直径和微血管侵犯)开发了无复发生存列线图,在训练队列(C指数:0.717)和测试队列(C指数:0.701)中具有良好的预测性能。与BCLC分期系统相比,C指数(训练队列:OS和RFS分别为0.787对0.678、0.717对0.675;外部队列2:0.748对0.624、0.729对0.587;外部队列1:RFS为0.716对0.6

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b318/8919774/482957c5e5cf/fonc-12-843589-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b318/8919774/a9b850e601a8/fonc-12-843589-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b318/8919774/3a3ad7e4940e/fonc-12-843589-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b318/8919774/3280f40106b4/fonc-12-843589-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b318/8919774/0bd393ff4c5b/fonc-12-843589-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b318/8919774/482957c5e5cf/fonc-12-843589-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b318/8919774/a9b850e601a8/fonc-12-843589-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b318/8919774/3a3ad7e4940e/fonc-12-843589-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b318/8919774/3280f40106b4/fonc-12-843589-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b318/8919774/09c58764880a/fonc-12-843589-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b318/8919774/de16e0f63f7f/fonc-12-843589-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b318/8919774/482957c5e5cf/fonc-12-843589-g008.jpg

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