Meta-Analysis
Copyright ©The Author(s) 2025.
World J Gastrointest Oncol. Jun 15, 2025; 17(6): 105887
Published online Jun 15, 2025. doi: 10.4251/wjgo.v17.i6.105887
Table 1 Basic characteristics and quality assessment of included studies
Ref.
Country
Period
Medical center
Study type
TACE + LEN vs TACE + SOR, n
Gender (F/M), TACE + LEN
Gender (F/M), TACE + SOR
Age, TACE + LEN
Age, TACE + SOR
Quality
Ding et al[15], 2021China2018-2020Beijing Ditan HospitalR32 vs 327/255/2757 ± 1156 ± 115
Xue et al[16], 2021China2017-2020First Affiliated Hospital of Sun Yat-Sen UniversityRCT50 vs 1004/463/9754 (49-61)54 (49-63)6
Xu et al[17], 2023China2019-2021First Affiliated Hospital of Anhui Medical UniversityR43 vs 4118/2517/2455 ± 12.2652.5 ± 11.476
Yang et al[18], 2021China2017-2020West China Medical SchoolR38 vs 384/344/3455.18 ± 10.9454.39 ± 12.17NA
Zhang et al[19], 2022China2018-2021The First Affiliated Hospital with Nanjing Medical UniversityR53 vs 599/447/5257.7 ± 11.858.8 ± 11.17
Zhao et al[20], 2022China2018-2020Chinese People’s Liberation Army General Hospital, BeijingR32 vs 291/314/2557.38 ± 9.4455.90 ± 8.187
Table 2 Other basic characteristics and quality assessment of included studies
Ref.
Prior HBV infection, TACE + LEN1
Prior HBV infection, TACE + SOR1
ECOG-PS (0-1/2), TACE + LEN
ECOG-PS (0-1/2), TACE + SOR
Child-Pugh (A/B), TACE + LEN
Child-Pugh (A/B), TACE + SOR
Invading blood vessels, TACE + LEN1
Invading blood vessels, TACE + SOR1
Distant metastasis, TACE + LEN1
Distant metastasis, TACE + SOR1
AFP (< 400/≥ 400, ng/mL), TACE + LEN
AFP (< 400/≥ 400, ng/mL), TACE + SOR
Ding et al[15], 202130/229/324/722/1022/1028/432/032/019/1323/916/1614/18
Xue et al[16], 202146/497/337/1384/1641/984/1636/1481/1927/2345/55NANA
Xu et al[17], 202338/536/520/2323/1832/1128/1317/2615/2611/3212/2923/2026/15
Yang et al[18], 202136/234/427/1127/1137/137/114/2415/23
Zhang et al[19], 202250/355/443/1045/1452/157/236/1741/1836/1739/2020/3325/34
Zhao et al[20], 202222/121/1112/1118/1419/427/510/1318/141/2222/10NANA
Table 3 Tumor response rate and long-term outcome
Measured outcomes
Studies, n
Heterogeneity test, I2 (%)
Heterogeneity test, P value
Model
RR/HR
95%CI
P value
Complete response600.95Random1,811.11-2.960.02
Partial response600.78Random1.381.12-1.700.002
Stable disease6500.08Random0.890.60-1.330.58
Progressive disease600.67Random0.540.39-0.740.0002
Objective response rate600.80Random1.471.24-1.74< 0.0001
Disease control rate682< 0.0001Random1.221.00-1.490.05
Overall survival439.80.173Random0.280.19-0.42< 0.05
Disease free survival400.482Random0.540.42-0.69< 0.05
Table 4 Adverse events
Adverse events
Studies, n
Heterogeneity test, I2(%)
Heterogeneity test, P value
Model
RR
95%CI
P value
All adverse events300.53Random0.970.79-1.200.80
Abdominal pain400.68Random0.950.65-1.410.81
Fever300.66Random0.950.72-1.250.69
Fatigue400.68Random1.280.79-2.050.32
Nausea and vomiting500.70 Random1.250.85-1.830.25
Decreased appetite500.76Random1.180.81-1.710.40
Liver dysfunction400.46Random1.040.62-1.750.87
Hypertension500.44Random2.531.19-5.390.02
Hand-foot skin reaction5750.003Random0.740.18-3.040.68
Diarrhea6390.16Random1.380.55-3.440.49
Thrombocytopenia300.71Random1.180.71-1.980.52
Rash6650.04Random0.880.19-4.160.88