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. Author manuscript; available in PMC: 2018 Apr 1.
Published in final edited form as: JAMA Oncol. 2017 Apr 1;3(4):493–500. doi: 10.1001/jamaoncol.2016.5116

Table 1.

Clinical Characteristics of the Study Participantsa

Characteristic Cohort P Value
Development (n = 721) Validation (n = 340)
At the Time of HCC Diagnosis
Age, median (IQR), y 58.2 (53.3–63.9) 56.4 (51.7–61.0) <.001
Male sex 542 (75.2) 283 (83.2) <.001
Liver disease
 Hepatitis C 424 (58.8) 191 (56.2) <.001
 Hepatitis B 116 (16.1) 78 (22.9)
 Fatty liver disease 63 (8.7) 11 (3.2)
 Alcoholic liver disease 62 (8.6) 45 (13.2)
 Others 56 (7.8) 15 (4.4)
MELD score, median (IQR) 11 (9–14) 11 (8–14) .79
HCC
 1 498 (69.1) 260 (76.5) .02
 2 167 (23.2) 53 (15.6)
 3 56 (7.8) 27 (7.9)
AFP, median (IQR), ng/mL 12.0 (5.0–54.5) 11.0 (5.0–41.0) .82
While on Wait List
Received LRT 660 (91.5) 221 (65.0) <.001
Wait time to LT, median (IQR), mo 8.1 (4.1–14.2) 10.5 (6.0–18.0) <.001
At the Time of LT
AFP, median (IQR), ng/mLb 8.3 (4.0–29.0) 9.4 (4.5–36.0) .21
 ≤20 482 (70.0) 221 (65.0)
 21–99 126 (18.2) 72 (21.2)
 100–999 66 (9.6) 36 (10.6)
 ≥1000 15 (2.2) 11 (3.2)
Pathologic stage
 No residual tumor 199 (27.6) 48 (14.1) <.001
 Within Milan criteria 363 (50.3) 165 (48.5)
 Beyond Milan criteria 159 (22.1) 127 (37.3)
Largest viable tumor diameter (cm) + No. of tumors, median (IQR) 3.5 (0–5.3) 4.5 (3.0–6.7) <.001
Microvascular invasion 68 (9.4) 81 (23.8) <.001
Histologic gradec
 Completely necrotic 199 (28.0) 48 (14.7) <.001
 Well differentiated 200 (28.1) 28 (8.6)
 Moderately differentiated 238 (33.4) 218 (66.9)
 Poorly differentiated 75 (10.5) 32 (9.8)

Abbreviations: AFP, α-fetoprotein; HCC, hepatocellular carcinoma; IQR, interquartile range; LRT, locoregional therapy; LT, liver transplantation; MELD, Model for End-Stage Liver Disease.

a

Unless otherwise noted, data are reported as number (percentage) of participants

b

For development cohort, n = 689.

c

For development cohort, n = 712; for validation cohort, n = 326.