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Resubclassification and clinical management for Barcelona Clinic Liver Cancer Stage C hepatocellular carcinoma

Authors
Lin, Chih-WenChen, Yaw-SenLo, Gin-HoWu, Tsung-ChinYeh, Jen-HaoYeh, Ming-LunDai, Chia-YenHuang, Jee-FuChuang, Wan-LongRoberts, LewisJun, Dae WonToyoda, HidenoriYasuda, SatoshiNguyen, Mindie H.Yu, Ming-Lung
Issue Date
Aug-2021
Publisher
SPRINGER
Keywords
Hepatocellular carcinoma; Advanced stage; Substage; Predictive factors; Prognosis; Overall survival; Treatment; Surgical resection; Target therapy; Immunotherapy
Citation
HEPATOLOGY INTERNATIONAL, v.15, no.4, pp.946 - 956
Indexed
SCIE
SCOPUS
Journal Title
HEPATOLOGY INTERNATIONAL
Volume
15
Number
4
Start Page
946
End Page
956
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/141439
DOI
10.1007/s12072-021-10169-8
ISSN
1936-0533
Abstract
Background Patients with Barcelona Clinic Liver Cancer Stage C (BCLC-C) hepatocellular carcinoma (HCC) can be markedly heterogeneous with varying prognosis. This study aims to establish a new subclassification system for BCLC-C HCC to better predict overall survival (OS) and to tailor therapy. Methods We retrospectively studied 1856 BCLC-C HCC patients between 2006 and 2017 from E-Da Hospital, Taiwan (n = 622, training cohort), Kaohsiung Medical University Hospital, Taiwan (n = 774, Taiwan validation cohort), and Stanford University Medical Center and Mayo Clinic (United States), Hanyang University Hospital (South Korea), and Ogaki Municipal Hospital (Japan) to make up the international validation cohort (n = 460). Results In the training cohort, significant factors associated with OS were largest tumor size >= 10 cm, extrahepatic spread, macrovascular invasion, and Child-Pugh class, which provided the basis, together with aged >= 75 years, for the substaging, through C0 to C4, of BCLC-C HCC patients. The median OS for substages C0, C1, C2, C3, and C4 were 43.8 months (95% confidence interval [CI] 32.2-53.7), 20.6 months (CI 14.1-25.9), 11.5 months (CI 8.02-14.1), 5.7 months (CI 4.02-5.98), and 3.2 months (CI 2.41-3.59), respectively, (p < 0.05). OS remained distinct among the proposed substages in the Taiwan validation cohort as well as the international validation cohort. The distinction between the substages persisted in subgroup analysis by substage combined with treatment modality. In substage C0-C3, patients receiving HCC curative therapy had a significantly better median OS than those receiving sorafenib or palliative therapy. Conclusion Our new substaging system provides more precise prognosis to better tailor therapy for BCLC-C HCC patients.
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