Impact of serum vascular endothelial growth factor on prognosis in patients with unresectable hepatocellular carcinoma after transarterial chemoembolization

被引:25
作者
Guo, Jian-hai [1 ]
Zhu, Xu [1 ]
Li, Xiao-ting [1 ]
Yang, Ren-jie [1 ]
机构
[1] Peking Univ, Sch Oncol, Beijing Canc Hosp & Inst,Dept Intervent Therapy, Key Lab Carcinogenesis & Translat Res,Minist Educ, Beijing 100142, Peoples R China
关键词
Hepatocellular carcinoma; Vascular endothelial growth factor; TACE; ELISA; LIVER-TRANSPLANTATION; FACTOR EXPRESSION; SURVIVAL ANALYSIS; THERMAL ABLATION; ANGIOGENESIS; CANCER; VEGF; NEOVASCULARIZATION; INVASIVENESS; RECURRENCE;
D O I
10.1007/s11670-012-0036-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To investigate the expression level of serum vascular endothelial growth factor (VEGF) in patients with unresectable hepatocellular carcinoma (HCC) and its relationship with the clinicopathological characteristics, and to assess the impact of serum VEGF as a predictive factor for HCC prognosis during transarterial chemoembolization (TACE) treatments. Serum VEGF levels were measured using enzyme-linked immunosorbent assay (ELISA) in 60 random patients who underwent TACE or transarterial infusion (TAI) for unresectable HCC between May and September 2008 and 12 healthy volunteers were also involved in this study to serve as control. All patients' clinicopathological features were retrospectively analyzed. Serum VEGF levels were correlated with clinicopathological features of the HCC patients. The patients' survival rates were analyzed with Kaplan-Meier survival curves and compared by the log-rank test. The prognostic significance of serum VEGF levels and factors related to survival rate were evaluated by univariate and multivariate analysis. The median serum VEGF level in the HCC patients was 285 pg/ml (range 14-1,207 pg/ml), significantly higher than that of healthy controls (P=0.021). The serum VEGF levels were significantly correlated with platelet counts (r=0.396, P=0.002) but not other clinicopathological features. Patients with serum VEGF level > 285 pg/ml had worse overall survival compared with those with serum VEGF level < 285 pg/ml (P=0.002). By multivariate analysis, the serum VEGF level was a significant prognostic factor. High serum VEGF levels may predict poor prognosis of HCC after TACE. This study highlights the importance of tumor biomarker as a prognostic predictor in TACE therapy for HCC, which has an intrinsic problem of unavailability of histopathological prognostic features.
引用
收藏
页码:36 / 43
页数:8
相关论文
共 39 条
  • [1] Predictors of survival after laparoscopic radiofrequency thermal ablation of hepatocellular cancer - A prospective study
    Berber, E
    Rogers, S
    Siperstein, A
    [J]. SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES, 2005, 19 (05): : 710 - 714
  • [2] Chemoembolization for hepatocellular carcinoma
    Bruix, J
    Sala, M
    Llovet, JM
    [J]. GASTROENTEROLOGY, 2004, 127 (05) : S179 - S188
  • [3] Management of hepatoceullular carcinoma
    Bruix, J
    Sherman, M
    [J]. HEPATOLOGY, 2005, 42 (05) : 1208 - 1236
  • [4] Management of Hepatocellular Carcinoma: An Update
    Bruix, Jordi
    Sherman, Morris
    [J]. HEPATOLOGY, 2011, 53 (03) : 1020 - 1022
  • [5] High eIF4E, VEGF, and microvessel density in stage I to III breast cancer
    Byrnes, K
    White, S
    Chu, QY
    Meschonat, C
    Yu, H
    Johnson, LW
    DeBenedetti, A
    Abreo, F
    Turnage, RH
    McDonald, JC
    Li, BD
    [J]. ANNALS OF SURGERY, 2006, 243 (05) : 684 - 692
  • [6] Chung In-Kwon, 2005, Korean J Hepatol, V11, P371
  • [7] Cooper BC, 2002, CLIN CANCER RES, V8, P3193
  • [8] The development and application of functional nuclear magnetic resonance to in vivo therapeutic anticancer research
    Dzik-Jurasz, A
    [J]. BRITISH JOURNAL OF RADIOLOGY, 2004, 77 (916) : 296 - 307
  • [9] Hepatocellular carcinoma: Epidemiology and molecular carcinogenesis
    El-Serag, Hashem B.
    Rudolph, Lenhard
    [J]. GASTROENTEROLOGY, 2007, 132 (07) : 2557 - 2576
  • [10] The seed and soil hypothesis: vascularisation and brain metastases
    Fidler, IJ
    Yano, S
    Zhang, RD
    Fujimaki, T
    Bucana, CD
    [J]. LANCET ONCOLOGY, 2002, 3 (01) : 53 - 57