Table 2 Baseline characteristics of the patients, tumors, and initial treatment options.

From: Development of machine learning-based clinical decision support system for hepatocellular carcinoma

Characteristics

All patients

(N = 1,021)

Derivation set

(N = 813)

Validation set

(N = 208)

Age, year

 

56.9 ± 10.5

56.9 ± 10.4

57.0 ± 10.8

Gender

Male

835 (81.8)

658 (80.9)

177 (85.1)

 

Female

186 (18.2)

155 (19.1)

31 (14.9)

ECOG performance status

0

767 (75.1)

615 (75.6)

152 (73.1)

 

1 or 2

224 (20.9)

164 (20.2)

50 (24.0)

 

3 or 4

40 (3.9)

34 (4.2)

6 (2.9)

Aetiology of liver disease

HBV

786 (77.0)

631 (77.6)

155 (74.5)

 

HCV

71 (7.0)

49 (6.0)

22 (10.6)

 

Others

164 (16.0)

133 (15.4)

31 (14.9)

Heavy alcohol consumption

Yes

168 (16.5)

130 (16.0)

38 (18.3)

Ascites

Present

173 (17.0)

143 (17.6)

30 (14.4)

Varices

Present

312 (30.6)

252 (30.9)

60 (28.8)

Child–Pugh class

A

779 (76.3)

620 (76.3)

159 (76.4)

 

B

205 (20.1)

163 (20.1)

42 (20.2)

 

C

37 (3.6)

30 (3.6)

7 (3.4)

Body mass index, kg/m2

 

24.0 (22.1–26.0)

24.0 (22.1–26.0)

24.0 (22.1–25.8)

Tumour number

1

595 (58.3)

471 (57.9)

124 (59.6)

 

2–3

217 (21.2)

178 (22.9)

39 (18.7)

 

 ≥ 4

209 (20.5)

164 (20.2)

45 (21.6)

Maximal tumour size, cm

 

4.0 (2.3–8.5)

4.0 (2.3–8.6)

4.0 (2.5–7.6)

Distribution

Single segmental

475 (46.5)

378 (46.5)

98 (47.1)

 

Unilobar

245 (24.0)

196 (24.1)

49 (23.6)

 

Bilobar

300 (29.4)

239 (29.4)

61 (29.3)

Distant metastasis

Present

125 (12.2)

99 (12.2)

26 (12.6)

Vascular invasion

Unilateral

150 (14.7)

115 (14.1)

35 (16.8)

 

Main or bilateral

83 (8.1)

65 (8.0)

18 (8.7)

RFA feasibility

Feasible

226 (22.1)

183 (22.5)

43 (20.7)

BCLC stage

0

134 (13.1)

102 (12.5)

32 (15.4)

 

A

265 (26.0)

218 (26.8)

47 (22.6)

 

B

184 (18.0)

152 (18.7)

32 (15.4)

 

C

374 (36.6)

287 (35.3)

87 (41.8)

 

D

64 (6.3)

54 (6.6)

10 (4.8)

Laboratory findings

AFP, ng/mL

42.1 (6.7–838.2)

41.9 (7.0–827.3)

42.4 (6.9–636.1)

 

Haemoglobin, g/dL

13.5 (12.2–14.6)

13.5 (12.2–14.7)

13.5 (12.2–14.5)

 

Platelet count, × 109/mm3

143 (97–197)

145 (97–197)

138 (98–199)

 

ALT, U/L

37 (25–53)

37 (25–53)

39 (25–59)

 

Total bilirubin, mg/dL

1.0 (0.7–1.4)

1.0 (0.7–1.4)

1.0 (0.8–1.5)

 

Albumin, mg/dL

3.6 (3.2–4.0)

3.6 (3.2–4.0)

3.7 (3.2–4.0)

 

Prothrombin time, INR

1.07 (1.01–1.17)

1.07 (1.01–1.17)

1.07 (1.01–1.18)

 

Creatinine, mg/dL

0.8 (0.7–0.9)

0.8 (0.7–0.9)

0.8 (0.7–0.9)

Initial treatment

Transplantation

46 (4.5)

36 (4.4)

10 (4.8)

 

Resection

336 (32.9)

268 (33.0)

68 (32.7)

 

RFA or PEIT

77 (7.5)

61 (7.5)

16 (7.7)

 

TACE

322 (31.5)

254 (31.2)

68 (32.7)

 

TACE combined with EBRT

67 (6.6)

53 (6.5)

14 (6.7)

 

Sorafenib treatment

31 (3.0)

24 (3.0)

7 (3.4)

 

Supportive care

103 (10.1)

86 (10.6)

17 (8.2)

 

Other therapies

39 (3.8)

31 (3.8)

8 (3.8)

  1. AFP alpha-fetoprotein, ALT alanine aminotransferase, BCLC barcelona clinic liver cancer, EBRT external beam radiotherapy, ECOG Eastern Cooperative Oncology Group, HBV hepatitis B virus, HCV hepatitis C virus, INR international normalized ratio, PEIT percutaneous ethanol injection, RFA radiofrequency ablation, TACE transarterial chemoembolization.
  2. *Variables are presented as mean ± standard deviation or median (IQR).
  3. RFA feasibility was defined as a size or location of the tumor to receive percutaneous RFA successfully without significant complications.