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

IF 4.4 3区 医学 Q2 ONCOLOGY Targeted Oncology Pub Date : 2024-11-01 Epub Date: 2024-10-03 DOI:10.1007/s11523-024-01103-7
Sejin Kim, Suat Ying Lee, Jaekyung Cheon, Hyung-Don Kim, Young Gyu Park, Joycelyn Jie Xin Lee, Min-Hee Ryu, Baek-Yeol Ryoo, David Tai, Changhoon Yoo
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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.

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病因对晚期肝细胞癌患者使用阿特珠单抗联合贝伐单抗疗效的影响:亚太地区多国回顾性分析。
背景:阿特珠单抗-贝伐单抗是治疗不可切除肝细胞癌(uHCC)的标准一线疗法。鉴于 HCC 病因的多样性及其对肿瘤微环境的潜在影响,了解不同肝病病因如何影响疗效非常重要:我们评估了肝病病因对阿特珠单抗-贝伐单抗疗效的影响,并评估了阿特珠单抗-贝伐单抗治疗期间肝功能的变化:本研究纳入了2016年7月至2023年3月期间韩国牙山医疗中心和新加坡国立癌症中心接受一线atezolizumab-贝伐单抗治疗的390名uHCC患者。患者被分为病毒组、代谢功能障碍相关肝病(MASLD)组和非病毒/非MASLD组。白蛋白胆红素(ALBI)评分在基线、第六周期前的每两个周期以及疾病进展时记录:大多数患者的病因是病毒(74.1%),17.2%的患者患有MASLD。不同病因组(病毒性与MASLD性与非病毒性/非MASLD性)的客观反应率(分别为23.2%对29.9%对23.5%;P=0.515)、无进展生存期(中位5.4个月对7.7个月对6.0个月;P=0.320)和总生存期(18.1个月对18.9个月对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 评分明显高于基线时的评分。与ALBI分级为1级或2级的患者相比,疾病进展时ALBI分级为3级的患者接受后续治疗的频率明显降低(48.4%对78.8%,p = 0.002):无论HCC病因如何,阿特珠单抗-贝伐单抗都具有一致的疗效,支持将其作为不同患者群体的一线治疗药物。肝功能评估仍是管理治疗和预测疗效的关键。
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
Targeted Oncology
Targeted Oncology 医学-肿瘤学
CiteScore
8.40
自引率
3.70%
发文量
64
审稿时长
>12 weeks
期刊介绍: Targeted Oncology addresses physicians and scientists committed to oncology and cancer research by providing a programme of articles on molecularly targeted pharmacotherapy in oncology. The journal includes: Original Research Articles on all aspects of molecularly targeted agents for the treatment of cancer, including immune checkpoint inhibitors and related approaches. Comprehensive narrative Review Articles and shorter Leading Articles discussing relevant clinically established as well as emerging agents and pathways. Current Opinion articles that place interesting areas in perspective. Therapy in Practice articles that provide a guide to the optimum management of a condition and highlight practical, clinically relevant considerations and recommendations. Systematic Reviews that use explicit, systematic methods as outlined by the PRISMA statement. Adis Drug Reviews of the properties and place in therapy of both newer and established targeted drugs in oncology.
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