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影响病因学对晚期肝细胞癌患者接受阿特珠单抗联合贝伐珠单抗疗效结局的影响:亚太地区的一项多国回顾性分析。

Impact of Etiology on Efficacy Outcomes with Atezolizumab Plus Bevacizumab in Patients with Advanced Hepatocellular Carcinoma: A Multinational Retrospective Analysis in Asia-Pacific.

机构信息

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea.

Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.

出版信息

Target Oncol. 2024 Nov;19(6):917-923. doi: 10.1007/s11523-024-01103-7. Epub 2024 Oct 3.

Abstract

BACKGROUND

Atezolizumab-bevacizumab is a standard first-line treatment for unresectable hepatocellular carcinoma (uHCC). Given the diversity in HCC etiology and its potential impact on the tumor microenvironment, understanding how different liver disease etiologies affect treatment efficacy is important.

OBJECTIVE

We assessed the influence of liver disease etiology on the efficacy of atezolizumab-bevacizumab and evaluated changes in liver function during treatment with atezolizumab-bevacizumab.

PATIENTS AND METHODS

This study included 390 patients with uHCC treated with first-line atezolizumab-bevacizumab from Asan Medical Center, South Korea, and National Cancer Centre Singapore, Singapore from July 2016 to March 2023. Patients were classified to viral, metabolic dysfunction-associated liver disease (MASLD) and nonviral/non-MASLD groups. Albumin-bilirubin (ALBI) scores were recorded at baseline and every two cycles up to cycle six and at the time of disease progression.

RESULTS

The majority of patients presented with viral etiologies (74.1%), and 17.2% had MASLD. Across etiological groups (viral versus MASLD versus nonviral/non-MASLD) no significant differences in objective response rate (23.2% versus 29.9% versus 23.5%, respectively; p = 0.515), progression-free survival (median 5.4 versus 7.7 versus 6.0 months; p = 0.320), and overall survival (18.1 versus 18.9 versus 14.4 months; p = 0.400) were observed. Among the patients with disease progression, ALBI scores at the time of progression were significantly higher than at baseline. Subsequent therapy was administered significantly less often to patients with ALBI grade 3 at disease progression compared with those with ALBI grades 1 or 2 (48.4% versus 78.8%, p = 0.002) CONCLUSIONS: Atezolizumab-bevacizumab demonstrates consistent efficacy regardless of HCC etiology, supporting its use as a first-line treatment across diverse patient populations. Liver function assessments remain crucial for managing therapy and predicting outcomes.

摘要

背景

阿替利珠单抗联合贝伐珠单抗是不可切除肝细胞癌(uHCC)的标准一线治疗药物。鉴于 HCC 的病因多样性及其对肿瘤微环境的潜在影响,了解不同的肝病病因如何影响治疗效果非常重要。

目的

我们评估了肝病病因对阿替利珠单抗联合贝伐珠单抗疗效的影响,并评估了阿替利珠单抗联合贝伐珠单抗治疗期间肝功能的变化。

患者和方法

本研究纳入了 2016 年 7 月至 2023 年 3 月期间,来自韩国首尔峨山医疗中心和新加坡国家癌症中心的 390 例接受一线阿替利珠单抗联合贝伐珠单抗治疗的 uHCC 患者。患者被分为病毒性、代谢相关脂肪性肝病(MASLD)和非病毒性/非 MASLD 组。在基线和每两个周期(最多至第 6 个周期)以及疾病进展时记录白蛋白-胆红素(ALBI)评分。

结果

大多数患者为病毒性病因(74.1%),17.2%为 MASLD。在病因学组(病毒性与 MASLD 与非病毒性/非 MASLD)中,客观缓解率(分别为 23.2%、29.9%和 23.5%;p=0.515)、无进展生存期(中位数 5.4 个月、7.7 个月和 6.0 个月;p=0.320)和总生存期(18.1 个月、18.9 个月和 14.4 个月;p=0.400)均无显著差异。在疾病进展的患者中,进展时的 ALBI 评分明显高于基线。与 ALBI 分级 1 或 2 的患者相比,ALBI 分级 3 的患者进展时接受后续治疗的比例显著降低(48.4%与 78.8%;p=0.002)。

结论

阿替利珠单抗联合贝伐珠单抗的疗效不受 HCC 病因的影响,支持其在不同患者人群中作为一线治疗药物的使用。肝功能评估对于管理治疗和预测结局仍然至关重要。

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