Surveillance Strategy for Barcelona Clinic Liver Cancer B Hepatocellular Carcinoma Achieving Complete Response: An Individualized Risk-Based Machine Learning Study

被引:5
作者
Chen, Qi-Feng [1 ,2 ,3 ]
Dai, Lin [4 ]
Wu, Ying [1 ,2 ,3 ]
Huang, Zilin [1 ]
Chen, Minshan [5 ]
Zhao, Ming [1 ]
机构
[1] Sun Yat Sen Univ, Dept Med Imaging & Intervent Radiol, Canc Ctr, Guangzhou, Peoples R China
[2] State Key Lab Oncol South China, Guangzhou, Peoples R China
[3] Collaborat Innovat Ctr Canc Med, Guangzhou, Peoples R China
[4] Sun Yat Sen Univ, Canc Prevent Ctr, Canc Ctr, Guangzhou, Peoples R China
[5] Sun Yat Sen Univ, Dept Liver Surg, Canc Ctr, Guangzhou, Peoples R China
来源
FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY | 2021年 / 9卷 / 09期
基金
中国国家自然科学基金;
关键词
Barcelona clinic liver cancer B; hepatocellular carcinoma; complete response; surveillance strategy; machine learning; TRANSARTERIAL CHEMOEMBOLIZATION; HEPATECTOMY; THERAPY;
D O I
10.3389/fbioe.2021.667641
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: For patients with complete response (CR) of Barcelona Clinical Liver Cancer (BCLC) stage B hepatocellular carcinoma (HCC), there is no consensus regarding the monitoring strategy. Optimal surveillance strategies that can detect early progression of HCC within a limited visit after treatment have not yet been investigated. A retrospective, real-world study was conducted to investigate surveillance strategies for BCLC stage B HCC (BBHCC) patients with CR after curative treatment to support clinical decision making. Methods: From January 2007 to December 2019, 546 BBHCC patients with CR after radical treatment were collected at Sun Yat-sen University Cancer Center. Seventy percent of patients were subjected to the train cohort randomly; the remaining patients comprised the validation cohort to verify the proposed arrangements. The random survival forest method was applied to calculate the disease progression hazard per month, and follow-up schedules were arranged to maximize the capability of progression detection at each visit. The primary endpoint of the study was the delayed-detection months for disease progression. Results: The cumulative 1, 2, and 3-years risk-adjusted probabilities for the train/ validation cohorts were 32.8%/33.7%, 54.0%/56.3%, and 64.0%/67.4%, respectively, with peaks around approximately the 9th month. The surveillance regime was primarily concentrated in the first year posttreatment. The delayed-detection months gradually decreased when the total follow-up times increased from 6 to 11. Compared with controls, our schedule reduced delayed detection. Typically, the benefits of our surveillance regimes were obvious when the patients were followed seven times according to our schedule. The optional schedules were 5, 7, 9, 11, 17, 23, and 30 months. Conclusion: The proposed new surveillance schedule may provide a new perspective concerning follow-up for BBHCC patients with CR.
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页数:8
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