A simple ABC score for prognosis stratification and treatment selection in advanced hepatocellular carcinoma.
Abstract
511 Background: Atezolizumab plus bevacizumab (A+B) is widely used as a standard first-line therapy for advanced hepatocellular carcinoma (HCC), while lenvatinib (L) and lenvatinib plus immunotherapy (L+I) remain common alternatives in clinical practice. Some patients have poor responses to A+B, and predictive biomarkers are lacking. We aimed to develop a simple blood-based prognostic score to aid in prognosis stratification and clinical decision-making. Methods: This retrospective international study included HCC patients treated with A+B, L, or L+I at 11 hospitals in Japan and 15 hospitals in Taiwan. Cox regression analysis was used to identify key prognostic factors for overall survival (OS). Results: Between September 2017 and March 2024, 1442 HCC patients were included, with a median age of 67.9 years and 77.7% being male. Multivariable analysis identified three independent poor prognostic factors, which were integrated into the ABC score: baseline (A)lpha-fetoprotein >20 ng/mL (hazard ratio [HR] 1.79; p<0.001), al(B)umin <3.5 g/dL (HR 1.71; p<0.001), and (C)hronic inflammation (neutrophil-to-lymphocyte ratio [NLR] >4; HR 1.50; p<0.001). Patients were distributed among ABC scores of 0 (242; 16.8%), 1 (551; 38.2%), 2 (483; 33.5%), and 3 (166; 11.5%), with corresponding median OS of 40.3, 22.7, 12.0, and 8.0 months, respectively (P<0.001). In the entire cohort, OS was similar across treatment regimens (median OS: 16.5 months for A+B, 20.1 months for L, and 17.7 months for L+I; P=0.087). However, among the 649 (45%) high-risk patients (ABC score 2–3), those treated with lenvatinib-based therapies had significantly better OS (median OS: 8.4 months for A+B, 11.0 months for L, and 13.7 months for L+I; P=0.0039). Conclusions: The ABC score is a simple and robust tool associated with survival in patients receiving first-line A+B or lenvatinib-based therapy. It may facilitate prognosis stratification and help clinical decision-making, but requires prospective validation. Multivariable Cox regression for overall survival. Variables HR 95% CI p-value Age 1.01 1.00–1.02 0.008 Sex (male vs. female) 0.87 0.73–1.03 0.106 ECOG Performance Status 0 — — — 1 1.35 1.15–1.59 <0.001 ≥2 1.89 1.46–2.44 <0.001 Vascular invasion (Yes vs. No) 1.50 1.27–1.76 <0.001 Extrahepatic spread (Yes vs. No) 1.21 1.04–1.41 0.014 AFP≥20 ng/ml (Yes vs. No) 1.79 1.52–2.11 <0.001 Albumin ≤ 3.5 g/dL (Yes vs. No) 1.71 1.46–1.99 <0.001 NLR≥4 (Yes vs. No) 1.50 1.29–1.75 <0.001 First-line treatment Lenvatinib + Immunotherapy — — — Lenvatinib monotherapy 0.83 0.66–1.03 0.090 Atezolizumab + bevacizumab 1.14 0.89–1.45 0.301 ECOG Performance Status: Eastern Cooperative Oncology Group Performance Status; AFP: alpha-fetoprotein; NLR: neutrophil-to-lymphocyte ratio.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Yung-Yeh Su
National Health Research Institute, Tainan, Taiwan
Masayuki Ueno
Po Ting Lin
Department of Gastroenterology and Hepatology, Chang Gung Medical Foundation, Linkou Chang Gung Memorial Hospital, Taoyuan City, Taiwan
Pei-Chang Lee
Division of Gastroenterology and Hepatology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan
Hiroki Morimura
Department of Gastroenterology and Hepatology, Osaka Red Cross Hospital, Osaka, Japan
Hong Wei Wang
School of Materials Science and Engineering, University of Science and Technology Beijing 1 , Beijing 100083,
Norihiro Nishijima
Department of Gastroenterology and Hepatology, Meiwa Hospital, Nishinomiya, Japan
Ching-Wei Chang
Satoru Iwamoto
Department of Gastroenterology, Kyoto Medical Center, Kyoto, Japan
Shu Nagatomo
Department of Gastroenterology and Hepatology, Tenri Hospital, Tenri, Japan
Takeshi Mitani
Department of Gastroenterology and Hepatology, Kurashiki Central Hospital, Kurashiki, Japan
Teng-Yu Lee
Haruhiko Takeda
Department of Gastroenterology and Hepatology, Graduate School of Medicine, Kyoto University
Atsushi Takai
Department of Gastroenterology and Hepatology, Graduate School of Medicine, Kyoto University
Hsueh-Chou Lai
China Medical University Hospital, Taichung, Taiwan
Hiroshi Seno
Department of Gastroenterology and Hepatology, Graduate School of Medicine, Kyoto University
Ying-Chun Shen
National Taiwan University Cancer Center, Taipei, Taiwan
Shi-Ming Lin
Yi-Hsiang Huang
Li-Tzong Chen
Kaohsiung Medical University Hospital, Kaohsiung, Taiwan