Table 1.
Patients (n = 55) | |
---|---|
Age (years), median (IQR) | 54 (46–62) |
Sex, n (%) | |
Male | 45 (81.8%) |
Female | 10 (18.2%) |
ECOG-PS, n (%) | |
0 | 47 (85.5%) |
1 | 8 (14.5%) |
Child-Pugh, n (%) | |
5 | 24 (43.6%) |
6 | 31 (56.4%) |
Hepatitis B infection, n (%) | |
Yes | 27 (49.1%) |
No | 28 (50.9%) |
HBV-DNA copy, n (%) | |
<2000 copy/mL | 31 (56.4%) |
≥2000 copy/mL | 19 (34.5%) |
Unknown | 5 (9.1%) |
AFP, n (%) | |
<400 ng/mL | 23 (41.8%) |
≥400 ng/mL | 32 (58.2%) |
PIVKA-II, n (%) | |
<400 mAU/mL | 7 (12.7%) |
≥400 mAU/mL | 47 (85.5%) |
Unknown | 1 (1.8%) |
PVTT type, n (%) | 37 (67.3%) |
I | 4 (7.3%) |
II | 26 (47.3%) |
III | 4 (7.3%) |
IV | 3 (5.5%) |
Extrahepatic metastasis, n (%) | |
Yes | 10 (18.2%) |
No | 45 (81.8%) |
Extrahepatic metastasis location, n (%) | |
Lung | 5 (9.1%) |
Lymph node | 4 (7.3%) |
Adrenal gland | 1 (1.8%) |
Tumour number, n (%) | |
Solitary | 32 (58.2%) |
Multiple | 23 (41.8%) |
Maximum tumour size (mm), mean ± SD | 101.7 ± 42.3 |
CNLC staging, n (%) | |
Ⅱa | 4 (7.3%) |
Ⅱb | 9 (16.4%) |
Ⅲa | 32 (58.2%) |
Ⅲb | 10 (18.2%) |
BCLC staging, n (%) | |
B | 12 (21.8%) |
C | 43 (78.2%) |
Duration of lenvatinib (months), median (IQR) | 2.6 (1.6–3.3) |
Cycles of camrelizumab, median (IQR) | 3 (2–4) |
Number of TACE, median (IQR) | 1 (1–2) |
ECOG-PS, Eastern Cooperative Oncology Group performance status; AFP, α-fetoprotein; PIVKA-II, protein induced by vitamin K absence-II; PVTT, portal vein tumour thrombosis; CNLC, China liver cancer staging; BCLC, Barcelona Clinic liver cancer stage; TACE, transcatheter arterial chemoembolisation.