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巴塞罗那临床肝癌分期 C 肝细胞癌的重新分类和临床管理。

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

机构信息

Division of Gastroenterology and Hepatology, E-Da Dachang Hospital, I-Shou University, Kaohsiung, Taiwan.

Division of Gastroenterology and Hepatology, E-Da Hospital, I-Shou University, Kaohsiung, Taiwan.

出版信息

Hepatol Int. 2021 Aug;15(4):946-956. doi: 10.1007/s12072-021-10169-8. Epub 2021 May 18.

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.

摘要

背景

巴塞罗那临床肝癌分期 C(BCLC-C)期的肝癌患者具有明显的异质性,预后差异很大。本研究旨在建立一种新的 BCLC-C 肝癌亚分类系统,以更好地预测总生存期(OS)并制定治疗方案。

方法

我们回顾性研究了 2006 年至 2017 年间来自中国台湾义大医院(n=622,训练队列)、高雄医学大学附设中和纪念医院(n=774,台湾验证队列)、斯坦福大学医学中心和梅奥诊所(美国)、汉阳大学医院(韩国)和大垣市民医院(日本)的 1856 例 BCLC-C 肝癌患者,构成国际验证队列(n=460)。

结果

在训练队列中,与 OS 显著相关的因素包括最大肿瘤直径≥10cm、肝外扩散、大血管侵犯和 Child-Pugh 分级,这些因素与年龄≥75 岁一起,为 BCLC-C 肝癌患者进行亚分期(C0 至 C4)提供了依据。亚分期 C0、C1、C2、C3 和 C4 的中位 OS 分别为 43.8 个月(95%置信区间[CI] 32.2-53.7)、20.6 个月(CI 14.1-25.9)、11.5 个月(CI 8.02-14.1)、5.7 个月(CI 4.02-5.98)和 3.2 个月(CI 2.41-3.59),差异有统计学意义(p<0.05)。在台湾验证队列和国际验证队列中,所提出的亚分期之间的 OS 仍然存在明显差异。在亚分期 C0-C3 中,接受肝癌根治性治疗的患者中位 OS 明显优于接受索拉非尼或姑息治疗的患者。

结论

我们的新亚分期系统为 BCLC-C 肝癌患者提供了更精确的预后,以便更好地制定治疗方案。

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