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巴塞罗那临床肝癌(BCLC)分期推荐对肝细胞癌患者生存率的影响。

The impact of BCLC recommendations on survival for patients with hepatocellular carcinoma.

作者信息

Iavarone Massimo, Alimenti Eleonora, Canova Lorenzo, Bruccoleri Mariangela, Antonelli Barbara, Ierardi Anna Maria, Sangiovanni Angelo, Cabibbo Giuseppe, De Silvestri Annalisa, Caccamo Lucio, Carrafiello Gianpaolo, Lampertico Pietro

机构信息

Division of Gastroenterology and Hepatology, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Department of Pathophysiology and Transplantation, CRC "A. M. and A. Migliavacca" Center for Liver Disease, University of Milan, Milan, Italy.

出版信息

Hepatol Commun. 2025 Jul 14;9(8). doi: 10.1097/HC9.0000000000000750. eCollection 2025 Aug 1.

Abstract

BACKGROUND

The Barcelona Clinic Liver Cancer (BCLC) system for HCC was updated in 2022. The aim of the study was to assess the suitability and impact on overall survival (OS) of BCLC_2022, along with "clinical decision-making" (CDM), using BCLC_2018 as a benchmark.

METHODS

We retrospectively evaluated 798 patients with de novo HCC followed prospectively from 2006 to 2022: 187 in BCLC 0, 371 in A, 132 in B, 87 in C, and 21 in D, all managed by a multidisciplinary team. Patients were followed until death or at the end of the follow-up period in December 2022.

RESULTS

The suitability of the algorithm increased from 51% for BCLC_2018 to 69% for BCLC_2022 (p<0.001). Among those treated with the newly introduced "lower priority options," 22% were in BCLC 0 and 37% in A, showing lower rates of complete response (CR) and shorter OS compared to first-line treatments. In BCLC 0 and A, CDM was associated with a significant decrease in "downward stage migration" with BCLC_2022 (from 33% to 16%, p<0.001). Conversely, in BCLC B and C, "upward stage migration" correlated with higher CR rates and longer OS [63 (36-72) vs. 28 (18-44) months, p=0.003 in BCLC B; 21 (15-44) vs. 11 (4-25) months, p<0.001 in BCLC C]. Independent predictors of mortality included AFP >200 ng/mL, Child-Pugh score C, advanced BCLC stage, and noncurative treatment.

CONCLUSIONS

BCLC_2022 and CDM provide greater flexibility in clinical practice without adversely affecting patient survival. Access to curative treatments improves the outcomes of selected patients in all stages.

摘要

背景

巴塞罗那临床肝癌(BCLC)系统于2022年进行了更新。本研究的目的是以BCLC_2018为基准,评估BCLC_2022以及“临床决策制定”(CDM)的适用性及其对总生存期(OS)的影响。

方法

我们回顾性评估了798例2006年至2022年期间前瞻性随访的初发性肝癌患者:BCLC 0期187例、A期371例、B期132例、C期87例、D期21例,均由多学科团队管理。对患者进行随访直至死亡或2022年12月随访期结束。

结果

该算法的适用性从BCLC_2018的51%提高到BCLC_2022的69%(p<0.001)。在接受新引入的“低优先级选项”治疗的患者中,BCLC 0期占22%,A期占37%,与一线治疗相比,其完全缓解(CR)率较低,总生存期较短。在BCLC 0期和A期,CDM与BCLC_2022的“向下分期迁移”显著减少相关(从33%降至16%,p<0.001)。相反,在BCLC B期和C期,“向上分期迁移”与更高的CR率和更长的总生存期相关[BCLC B期为63(36 - 72)个月 vs. 28(18 - 44)个月,p = 0.003;BCLC C期为21(15 - 44)个月 vs. 11(4 - 25)个月,p<0.001]。死亡的独立预测因素包括甲胎蛋白>200 ng/mL、Child-Pugh C级、晚期BCLC分期和非根治性治疗。

结论

BCLC_2022和CDM在临床实践中提供了更大的灵活性,且不会对患者生存产生不利影响。获得根治性治疗可改善所有分期中部分患者的预后。

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