Microvascular invasion has limited clinical values in hepatocellular carcinoma patients at Barcelona Clinic Liver Cancer (BCLC) stages 0 or B

被引:59
作者
Huang, Cheng [1 ,2 ]
Zhu, Xiao-Dong [1 ,2 ]
Ji, Yuan [3 ]
Ding, Guang-Yu [1 ,2 ]
Shi, Guo-Ming [1 ,2 ]
Shen, Ying-Hao [1 ,2 ]
Zhou, Jian [1 ,2 ]
Fan, Jia [1 ,2 ]
Sun, Hui-Chuan [1 ,2 ]
机构
[1] Fudan Univ, Key Lab Carcinogenesis & Canc Invas, Chinese Minist Educ, Liver Canc Inst, 136 Yi Xue Yuan Rd, Shanghai 200032, Peoples R China
[2] Fudan Univ, Key Lab Carcinogenesis & Canc Invas, Chinese Minist Educ, Zhongshan Hosp, 136 Yi Xue Yuan Rd, Shanghai 200032, Peoples R China
[3] Fudan Univ, Zhongshan Hosp, Dept Pathol, 136 Yi Xue Yuan Rd, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
Microvascular invasion; Barcelona Clinic Liver Cancer stage; Hepatocellular carcinoma; Prognosis; LONG-TERM SURVIVAL; RESECTION; MANAGEMENT; RECOMMENDATIONS; RECURRENCE; PROGNOSIS; SYSTEM;
D O I
10.1186/s12885-017-3050-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Microvascular invasion (MVI) is recognized as a prognostic factor associated with poor outcome in hepatocellular carcinoma (HCC) patients after curative resection. It remains unclear, however, whether MVI can provide prognostic information for patients at a specific tumor stage. Methods: Consecutive HCC patients who underwent curative resection in years of 2007 and 2008 (discovery cohort) were enrolled in this retrospective study. Patients were stratified by the Barcelona Clinic Liver Cancer (BCLC) staging system. The prognostic significance of MVI for overall survival (OS) and recurrence-free survival (RFS) was studied in each subgroup. The clinical significance of MVI was validated in another cohort of patients underwent curative surgery in the year of 2006 (validation cohort). Results: Of the 1540 patients in the discovery cohort, 389 (25.3%) patients had detectable MVI. Occurrence rates of MVI in the BCLC stage 0, A, and B subgroups were 12.4, 26.2, and 34.4%, respectively. In univariate analysis, MVI was associated with poor OS and RFS (P < 0.001 for both) in HCC patients at stage A, with poor OS in patients at stage 0 (P = 0.028), and with poor RFS at stage B (P = 0.039). In multivariate analysis, MVI was an independent risk factor for OS (HR = 1.431, 95% CI, 1.163-1.761, P < 0.001) and RFS (HR = 1.400, 95% CI, 1.150-1.705, P = 0.001) in patients at stage A; and an independent risk factor for RFS (P = 0.043) in patients at stage B. A similar clinical significance of MVI was found in the validation cohort. Conclusions: MVI has limited prognostic value for HCC patients at BCLC stages 0 and B. For those at stage A, MVI was associated with patient survival and may help to select patients with high risk of disease recurrence.
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页数:8
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