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. Author manuscript; available in PMC: 2024 Sep 1.
Published in final edited form as: J Hepatol. 2023 Sep 7;79(6):1469–1477. doi: 10.1016/j.jhep.2023.08.020

Table 2.

Explant characteristics on pathology by dual positivity for AFP-L3 ≥15% and DCP ≥7.5 ng/ml.

Overall (N = 285) Negative for dual biomarker elevation (n = 265) AFP-L3 ≥15% and DCP ≥7.5 ng/ml (n = 20) p value
Median largest viable tumor on explant (cm, IQR) 1.0 (0–1.8) 0.8 (0–1.7) 2.0 (1.6–2.9) <0.001
Median total viable tumor diameter on explant (cm, IQR) 1.2 (0–3.0) 1.0 (0–2.7) 4.9 (3.1–8.2) <0.001
Median number of viable HCC lesions on explant (n, IQR) 1.0 (0–2) 1.0 (0–2) 4.0 (2.5–5) <0.001
Vascular invasion (n, %) 13 (4.6) 5 (1.9) 8 (40.0) <0.001*
High risk pathology on explant (n, %) 47 (16.5) 30 (11.3) 17 (85.0) <0.001*
Explant outside Milan (n, %) 40 (14.0) 28 (10.6) 12 (60.0) <0.001*
RETREAT score (score, IQR) 1 (0–2) 1 (0–2) 3 (2–4) <0.001
Recurrence-free survival (HR, 95% CI) Reference 26.6 (10.3–68.9) <0.001Δ
Overall survival (HR, 95% CI) Reference 8.2 (3.4–19.6) <0.001Δ

AFP-L3, AFP bound to Lens culinaris agglutinin; DCP, des-gamma-carboxyprothrombin; HCC, hepatocellular carcinoma; HR, hazard ratio; RETREAT, risk estimation of tumor recurrence after transplant.

*

Chi squared test.

Two-sample exact Wilcoxon rank-sum (Mann-Whitney) test.

Δ

Cox proportional hazards test.