Table 1

Key clinical characteristics of patients with hepatobiliary cancer (n=187)

VariableICI cohort 1 (n=43)ICI cohort 2 (n=108)Non-ICI cohort (n=36)
Median age (range)61(27–82)59.5 (18–80)61.5 (34–84)
Sex—no. (%)
 Male30 (69.8)68 (63.0)26 (72.2)
 Female13 (30.2)40 (37.0)10 (27.8)
Histological type—no. (%)
 HCC12 (27.9)44 (40.7)11 (30.6)
 ICC19 (44.2)39 (36.1)11 (30.6)
 ECC4 (9.3)16 (14.8)7 (19.4)
 GBC5 (11.6)8 (7.4)6 (16.7)
 CHCC3 (7.0)1 (0.9)1 (2.8)
ECOG PS—no. (%)
 025 (58.1)40 (37.0)12 (33.3)
 112 (27.9)60 (55.6)18 (50)
 26 (14.1)8 (7.4)6 (16.7)
Child-Pugh grade—no. (%)
 A38 (88.4)95 (88.0)29 (80.6)
 B5 (11.6)11 (10.2)5 (13.9)
 C0 (0.0)2 (1.9)2 (5.6)
Tumor burden score—no. (%)
 ≥815 (34.9)42 (38.9)10 (27.8)
 <828 (65.1)66 (61.1)26 (72.2)
Number of prior systemic therapies for advanced metastatic disease—no. (%)
 028 (65.1)44 (40.7)24 (66.7)
 112 (27.9)39 (36.1)4 (11.1)
 2 and more3 (7.0)25 (23.1)8 (22.2)
Current therapy—no. (%)
 De novo combination PD-1 inhibitor with lenvatinib43 (100)32 (29.6)0 (0.0)
 Lenvatinib sequential PD-1 combination therapy0 (0.0)27 (25.0)0 (0.0)
 PD-1 inhibitor+other target therapy0 (0.0)49 (45.4)*0 (0.0)
 Target therapy monotherapy0 (0.0)0 (0.0)26 (72.2)†
 Others0 (0.0)0 (0.0)10 (27.8)
Follow-up—(IQR) month7.87 (5.8–11.3)11.05 (6.68–14.83)5.83 (3.44–8.26)
  • *Consists of apatinib (n=23), bevacizumab (n=5) and anlotinib (n=2), regorafenib (n=2), cabozantinib (n=2) and others.

  • †Lenvatinib (n=16), afatinib (n=2), olaparib (n=2) and others.

  • CHCC, combined hepatocellular-cholangiocarcinoma; ECC, extrahepatic cholangiocarcinoma; GBC, gallbladder cancer; HCC, hepatocellular carcinoma; ICC, intrahepatic cholangiocarcinoma; ICI, immune checkpoint inhibitor; PD-1, programmed cell death protein 1; PS, performance status.