Retrospective Study
Copyright ©The Author(s) 2016.
World J Gastroenterol. Apr 7, 2016; 22(13): 3632-3643
Published online Apr 7, 2016. doi: 10.3748/wjg.v22.i13.3632
Table 1 Characteristics of hepatocellular carcinoma patient with portal vein tumor thrombus invading the main portal vein trunk and inferior vena cava n (%)
Group 1 (n = 307)
Group 2(n = 54)Group 3(n = 15)Group 4(n = 42)P value
TACE(n = 274)TACE-sorafenib(n = 33)P value
Baseline characteristic
Age, mean ± SD48.62 ± 12.0949.51 ± 11.230.76447.40 ± 17.4849.78 ± 21.2651.49 ± 23.230.668
Sex (M)233 (85.0)26 (78.8)0.35046 (85.2)12 (80.0)36 (85.7)0.960
Clinical characteristic
Positive for HBsAg224 (81.8)29 (87.9)0.50546 (85.2)14 (93.3)36 (85.7)0.665
Positive for anti-HCV16 (5.8)0 (0.0)0.2341 (1.9)0 (0.0)1 (2.3)0.755
PLT (109/L)198.25 ± 88.17205.94 ± 102.040.146246.37 ± 71.13211.74 ± 101.21297.10 ± 148.070.654
TBil (μmol/L)19.1 (13.08-30.10)16.70 (11.80-23.00)0.34721.1 (11.46-32.37)17.23 (10.79-35.69)25.1 (10.78-41.76)0.065
ALB (g/L)37.29 ± 5.1437.74 ± 4.640.98139.31 ± 7.8136.73 ± 4.2732.13 ± 8.230.851
ALT (U/L)54.00 (35.00-79.00)52.00 (35.00-99.00)0.81352.00 (32.00-77.00)56.00 (31.00-72.00)58.00 (31.00-81.00)0.135
AST (U/L)79.00 (49.00-144.00)80.00 (50.00-157.50)0.84365.00 (28.00-101.00)78.00 (45.00-127.00)75.00 (21.00-167.00)0.104
PT (s)13.75 ± 1.5213.84 ± 1.9340.96312.11 ± 1.4113.49 ± 1.3713.79 ± 1.540.060
AFP (mg/L)873 (126-12100)1210 (123-12100)0.107745 (310-12100)691 (348-12100)1207 (1001-12100)0.793
Child-Pugh Score5 (5-8)5 (5-8)0.9145 (5-8)6 (5-8)6 (5-9)0.255
Ascites8 (2.9)0 (0.0)0.9990 (0.0)0 (0.0)3 (7.1)0.201
Pathological characteristic
Tumor size (cm)6.78 ± 2.967.14 ± 3.970.1017.13 ± 2.736.97 ± 2.377.95 ± 3.340.437
Tumor number (≥ 3), n178 (65.0)22 (66.7)0.84617 (32.4)9 (60.0)27 (64.2)0.982
Cirrhosis, n223 (81.0)27 (81.8)0.95246 (85.2)11 (73.3)36 (88.1)0.697
Portal vein hypertension, n76 (27.7)8 (24.2)0.67112 (22.2)3 (20.0)14 (33.3)0.609
Main portal vein trunk, n211 (77.0)21 (63.6)0.09144 (81.5)6 (77.0)17 (77.0)< 0.001
Inferior vena cava, n63 (23.0)12 (36.4)10 (18.5)9 (77.0)25 (77.0)
Table 2 Survival period and survival rate in different groups
Mean overall survival (mo)3-mo survival rate6-mo survival rate12-mo survival rate24-mo survival rate
TACE administration10.3994.1%85.9%51.5%0.0%
TACE subgroup10.2293.8%86.7%43.9%0.0%
TACE-sorafenib subgroup10.5295.3%83.3%53.8%0.0%
Liver resection + TACE4.1360.3%22.2%0.0%0.0%
Targeted therapy of sorafenib3.5450.9%29.5%0.0%0.0%
Palliate treatment2.8255.0%0.0%0.0%0.0%
Table 3 Complications and adverse events in different therapy groups n (%)
ComplicationGroup 1 (n = 307)
Group 2(n = 54)Group 3(n = 15)P value
TACE(n = 274)TACE-sorafenib (n = 33)P value
Nausea, vomiting49 (17.9)19 (57.6)< 0.00112 (22.2)12 (80.0)< 0.001
Fever62 (22.6)8 (24.2)0.83511 (20.4)0 (0.0)< 0.001
Pain119 (43.4)7 (21.2)0.04724 (44.4)0 (0.0)< 0.001
Alopecia3 (1.1)11 (33.3)< 0.0013 (5.6)6 (40.0)< 0.001
Bleeding of tumor rupture0 (0.0)2 (6.0)< 0.0010 (0.0)0 (0.0)< 0.001
Liver failure1 (0.4)25 (75.8)< 0.0015 (9.3)4 (26.7)< 0.001
Bile leakage0 (0.0)0 (0.0)0.9994 (7.4)0 (0.0)< 0.001
Bleeding of esophageal venous plexus0 (0.0)0 (0.0)0.9992 (3.7)0 (0.0)< 0.001
Gastrointestinal hemorrhage0 (0.0)1 (3.0)0.0041 (1.9)1 (6.7)< 0.001
Heart failure0 (0.0)0 (0.0)0.9991 (1.9)0 (0.0)< 0.001
Infection1 (0.4)0 (0.0)0.9991 (1.9)0 (0.0)< 0.001
Ectopic embolism syndrome1 (0.4)0 (0.0)0.9990 (0.0)0 (0.0)< 0.001
Refractory ascites0 (0.0)0 (0.0)0.9993 (5.6)0 (0.0)< 0.001
Pulmonary complication1 (0.4)1 (3.0)0.0727 (13.0)0 (0.0)< 0.001
Therapy-related death0 (0.0)0 (0.0)0.99951 (9.3)0 (0.0)< 0.001
Table 4 Adverse events related to sorafenib administration n (%)
Adverse eventMono-therapy of sorafenib
TACE combined with sorafenib
All eventsGrade 1-2 eventsGrade 3-4 eventsAll eventsGrade 1-2 eventsGrade 3-4 events
Overall incidence14 (93.3)12 (80.0)2 (13.3)30 (90.9)26 (78.8)4 (12.1)
Alopecia6 (40.0)6 (40.0)0 (0.0)11 (33.3)11 (33.3)0 (0.0)
Anorexia4 (26.7)4 (26.7)0 (0.0)18 (54.5)18 (54.5)0 (0.0)
Diarrhea13 (86.7)12 (80.0)1 (6.7)27 (81.8)26 (78.8)1 (3.0)
Epistaxis1 (6.7)1 (6.7)0 (0.0)2 (6.0)2 (6.0)0 (0.0)
Fatigue12 (80.0)12 (80.0)0 (0.0)22 (66.7)21 (63.6)1 (3.0)
Gastrointestinal hemorrhage1 (6.7)1 (6.7)0 (0.0)1 (3.0)1 (3.0)0 (0.0)
Hand-foot skin reactions11 (73.3)10 (66.7)0 (0.0)12 (36.3)11 (33.3)1 (3.0)
Liver dysfunction4 (26.7)4 (26.7)1 (6.7)25 (75.8)23 (69.7)2 (6.0)
Nausea12 (80.0)12 (80.0)0 (0.0)19 (57.6)19 (57.6)0 (0.0)
Table 5 Factors affecting overall survival using Cox’s proportional hazard model
FactorUnivariate analysis
Multivariate analysis
Patients, nMean OS (mo)95%CIP valueHR95%CIP value
Positive for HBsAg
Yes3499.058.33-9.760.0351.090.56-2.140.798
No6910.589.92-11.23
Positive for anti-HCV
Yes196.002.49-9.510.0261.450.44-3.880.454
No3999.428.90-9.94
AFP (mg/L)
> 4001347.996.94-9.05< 0.0011.841.09-3.110.023
≤ 4002849.969.42-10.49
Child-Pugh Stage
Stage A2629.889.34-10.42< 0.0011.991.20-3.300.008
Stage B1568.287.21-9.37
Tumor size (cm)
> 53018.487.79-9.18< 0.0013.311.57-6.980.002
≤ 511710.8210.20-11.45
Tumor number
> 31478.627.92-9.32< 0.0012.101.22-3.630.007
≤ 327110.559.89-11.20
Cirrhosis
Yes3438.858.23-9.460.0072.101.02-4.320.044
No7510.8210.06-11.59
Portal hypertension
Yes1137.006.03-7.98< 0.0011.651.02-2.650.041
No34510.149.62-10.65
Tumor thrombus location
Main portal vein trunk29910.409.89-10.91< 0.0014.512.66-7.65< 0.001
Inferior vena cava1194.834.26-5.41