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阿替利珠单抗联合贝伐珠单抗作为肝细胞癌一线系统治疗:一项多机构队列研究。

Atezolizumab plus bevacizumab as first-line systemic therapy for hepatocellular carcinoma: a multi-institutional cohort study.

机构信息

Department of Internal Medicine, Mayo Clinic, Rochester, MN, United States.

Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States.

出版信息

Oncologist. 2024 Nov 4;29(11):986-996. doi: 10.1093/oncolo/oyae142.

Abstract

BACKGROUND

Atezolizumab plus bevacizumab is the standard of care for advanced hepatocellular carcinoma (HCC) in the first-line setting, although was only evaluated in patients with Child-Pugh (CP) A liver function in the IMbrave150 trial. We sought to determine the outcomes of these patients based on CP score and ALBI grade in the US population.

METHODS

This multicenter cohort study included patients with HCC who received atezolizumab with bevacizumab as first-line systemic therapy between March 2018 and November 2023. Overall survival (OS) was determined using the Kaplan-Meier method and multivariate analyses were performed using Cox proportional hazard regression method.

RESULTS

Among 322 patients, 226, 86, and 10 patients had CP-A, CP-B, and CP-C liver function, respectively. Median age was 66.5 years, 78.6% were male, and 82.6% were White. Median OS (mOS) was 21.6 months for those with CP-A, 9.1 months for those with CP-B7, and 4.7 months for those with CP-B8-C12 (P < .0001). Among patients with CP-A, those with ALBI grade 1 had an mOS of 34.9 months versus 14.2 months in those with grade 2. In multivariate analyses, CP score, ALBI grade, hepatitis B, performance status, and macrovascular invasion were significantly associated with survival.

CONCLUSIONS

CP score is an important prognostic tool for patients with HCC receiving atezolizumab plus bevacizumab, and this regimen remains a viable option for patients with CP-B7 with no additional safety concern, although the benefit is significantly less than those with CP-A. ALBI score has independent predictive value in patients with CP-A liver function.

摘要

背景

阿替利珠单抗联合贝伐珠单抗是一线治疗晚期肝细胞癌(HCC)的标准治疗方法,但仅在 IMbrave150 试验中评估了肝功能为 Child-Pugh(CP)A 的患者。我们旨在根据 CP 评分和美国人群中的 ALBI 分级来确定这些患者的结局。

方法

这是一项多中心队列研究,纳入了 2018 年 3 月至 2023 年 11 月期间接受阿替利珠单抗联合贝伐珠单抗作为一线系统治疗的 HCC 患者。使用 Kaplan-Meier 法确定总生存期(OS),并使用 Cox 比例风险回归法进行多变量分析。

结果

在 322 名患者中,CP-A、CP-B 和 CP-C 肝功能的患者分别有 226、86 和 10 名。中位年龄为 66.5 岁,78.6%为男性,82.6%为白人。CP-A 患者的中位 OS(mOS)为 21.6 个月,CP-B7 患者为 9.1 个月,CP-B8-C12 患者为 4.7 个月(P<0.0001)。在 CP-A 患者中,ALBI 分级 1 的患者 mOS 为 34.9 个月,而 ALBI 分级 2 的患者为 14.2 个月。多变量分析显示,CP 评分、ALBI 分级、乙型肝炎、体能状态和大血管侵犯与生存显著相关。

结论

CP 评分是接受阿替利珠单抗联合贝伐珠单抗治疗的 HCC 患者的重要预后工具,尽管该方案对 CP-B7 患者没有额外的安全性担忧,但获益明显小于 CP-A 患者,该方案仍然是一种可行的选择。ALBI 评分在 CP-A 肝功能患者中有独立的预测价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c7/11546648/85f54a7e634d/oyae142_fig1.jpg

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