ALBI Grade Enables Risk Stratification for Bleeding Events and Refines Prognostic Prediction in Advanced HCC Following Atezolizumab and Bevacizumab.

IF 4.2 3区 医学 Q2 ONCOLOGY
Journal of Hepatocellular Carcinoma Pub Date : 2025-04-04 eCollection Date: 2025-01-01 DOI:10.2147/JHC.S462701
Bernardo Stefanini, Claudia Angela Maria Fulgenzi, Bernhard Scheiner, James Korolewicz, Jaekyung Cheon, Naoshi Nishida, Celina Ang, Thomas U Marron, Y Linda Wu, Anwaar Saeed, Brooke Wietharn, Lorenza Rimassa, Angelo Pirozzi, Antonella Cammarota, Tiziana Pressiani, Matthias Pinter, Lorenz Balcar, Yi-Hsiang Huang, Aman Mehan, Samuel Phen, Caterina Vivaldi, Francesca Salani, Gianluca Masi, Dominik Bettinger, Arndt Vogel, Martin Schönlein, Johann von Felden, Kornelius Schulze, Henning Wege, Adel Samson, Peter R Galle, Masatoshi Kudo, Giulia Francesca Manfredi, Ciro Celsa, Nichola Awosika, Alessio Cortellini, Amit G Singal, Rohini Sharma, Hong Jae Chon, Francesco Tovoli, Fabio Piscaglia, David James Pinato, Antonio D'Alessio
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引用次数: 0

Abstract

Background and aims: Atezolizumab and bevacizumab (A+B) are recommended for treating unresectable hepatocellular carcinoma (HCC). Although highly effective, A+B can lead to potentially life-threatening adverse events including bleeding. We investigated whether albumin-bilirubin (ALBI) grade identifies patients with a higher risk of bleeding and its impact on prognosis than the Child-Pugh (CP) score.

Methods: We performed a multicenter retrospective study of 15 tertiary referral centers that consecutively treated patients with A+B. We analyzed the association between the ALBI grade and gastrointestinal bleeding using the χ2 test. Overall survival (OS) stratified by ALBI was estimated using the Kaplan-Meier method and the predictive value for the 6-months OS landmark with ROC curves.

Results: Of the 368 patients included in the analysis, 163 (44.3%), 192 (52.2%) and 13 (3.5%) had ALBI 1, ALBI 2, and ALBI 3, respectively. ALBI grade was associated with a 3-fold increase in bleeding risk (3.1% in ALBI 1 vs 10.2% in ALBI 2/3, p=0.008). Among 192 patients with pre-treatment EGD, G2 and G3 varices were associated with an increased risk of bleeding, whereas G1 varices had a similar risk as no varices. Patients with ALBI 1 achieved a longer median OS (not reached; 95% CI, 24.9-33.7), than ALBI 2 (9.7 months; 95% CI, 7.0-12.3) or ALBI 3 (5.6 months; 95% CI, 0.1-12.0). ALBI outperformed the CP score for predicting 6-month OS with an AUC 0.79 of ALBI versus 0.71 for the CP score (p=0.01).

Conclusion: A Higher ALBI grade was associated with an increased risk of gastrointestinal bleeding after receiving A+B, and outperformed the CP score in predicting worse survival.

ALBI分级使出血事件的风险分层和阿特唑单抗和贝伐单抗后晚期HCC的预后预测更加精确。
背景和目的:Atezolizumab和bevacizumab (A+B)被推荐用于治疗不可切除的肝细胞癌(HCC)。虽然非常有效,但A+B可能导致潜在的危及生命的不良事件,包括出血。我们研究了白蛋白胆红素(ALBI)分级是否能识别出出血风险较高的患者及其对预后的影响,而不是Child-Pugh评分。方法:我们对连续治疗a +B患者的15个三级转诊中心进行了一项多中心回顾性研究。我们采用χ2检验分析ALBI分级与胃肠道出血之间的关系。采用Kaplan-Meier法估计ALBI分层的总生存期(OS),并采用ROC曲线预测6个月OS标尺的预测值。结果:纳入分析的368例患者中,ALBI 1型163例(44.3%),ALBI 2型192例(52.2%),ALBI 3型13例(3.5%)。ALBI分级与出血风险增加3倍相关(ALBI 1为3.1%,ALBI 2/3为10.2%,p=0.008)。在192名治疗前患有EGD的患者中,G2和G3静脉曲张与出血风险增加相关,而G1静脉曲张与无静脉曲张的风险相似。ALBI 1型患者的中位生存期较长(未达到;95% CI, 24.9-33.7),而ALBI 2(9.7个月;95% CI, 7.0-12.3)或ALBI 3(5.6个月;95% ci, 0.1-12.0)。ALBI在预测6个月OS方面优于CP评分,ALBI的AUC为0.79,而CP评分为0.71 (p=0.01)。结论:较高的ALBI分级与接受A+B治疗后消化道出血的风险增加相关,并且在预测较差的生存方面优于CP评分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.50
自引率
2.40%
发文量
108
审稿时长
16 weeks
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