无法切除的肝细胞癌在接受阿特珠单抗-贝伐单抗治疗后,可通过改用微波消融术获得治愈。

Journal of liver cancer Pub Date : 2024-09-01 Epub Date: 2024-06-03 DOI:10.17998/jlc.2024.05.23
Rene John D Febro, Engelbert Simon S Perillo, Akemi A Kimura, Stephen N Wong
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引用次数: 0

摘要

简介:阿特珠单抗/贝伐单抗是治疗不可切除肝细胞癌(uHCC)的推荐一线系统疗法,可通过切除术和局部治疗促进治愈性转归。然而,关于使用微波消融术(MWA)治愈转归的报道却很少。本研究旨在确定以阿特珠单抗-贝伐单抗作为一线疗法的微波消融治疗uHCC患者的治愈转化率,并比较治愈转化和未治愈转化患者的特征和生存情况:方法:纳入2021年5月至2023年12月在一家三级中心开始接受阿特珠单抗-贝伐单抗治疗的连续uHCC患者。客观反应(ORR)和疾病控制率(DCR)基于RECIST 1.1和mRECIST标准:结果:连续纳入了20例uHCC患者(60%为晚期),其中90%超过了up-to-7标准。采用RECIST和mRECIST标准,ORR和DCR分别为35%和60%,以及35%和55%。尽管中位 HCC 大小为 6.1 厘米(范围:2.4-7.3 厘米),但仍有 5 例(25%)患者通过 MWA 成功转为治愈(4 例晚期,1 例中期)。其中两名患者在首次服用阿特珠单抗-贝伐单抗132-133周后无肿瘤、无药物。接受根治性转归治疗的患者的生存期明显长于未接受根治性转归治疗的患者。(P=0.024)其他与生存相关的因素包括男性、Child-Pugh A级和客观反应:结论:尽管uHCC的肿瘤体积相对较大,但一线阿特珠单抗-贝伐单抗可成功实现MWA治愈性转归。然而,要确定这一策略是否普遍适用,还需要前瞻性多中心试验的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cure can be achieved by conversion to microwave ablation following atezolizumab-bevacizumab therapy in unresectable hepatocellular carcinoma.

Backgrounds/aims: Atezolizumab/bevacizumab is the recommended first-line systemic therapy for unresectable hepatocellular carcinoma (uHCC) and may facilitate curative conversion through resection and locoregional therapies. However, there have been very few reports on curative conversion using microwave ablation (MWA). This study aimed to determine the curative conversion rate with MWA using atezolizumab-bevacizumab as the first-line treatment in patients with uHCC, and to compare the characteristics and survival of patients with and without curative conversion.

Methods: Consecutive patients with uHCC who were started on atezolizumab-bevacizumab from May 2021 to December 2023 in a single tertiary center were included. Objective response rate (ORR) and disease control rate (DCR) were based on the Response Evaluation Criteria In Solid Tumors (RECIST) 1.1 and modified RECIST (mRECIST) criteria.

Results: Twenty consecutive patients with uHCC (60% advanced-stage) were included, 90% exceeding the up-to-7 criteria. The ORR and DCR were 35% and 60%, 35% and 55% using RECIST and mRECIST, respectively. Five patients (25%) underwent successful curative conversion with MWA (four advanced and one intermediate stage) despite a median HCC size of 6.1 cm (range, 2.4-7.3). Two of these patients were tumor and drug-free 132-133 weeks from the 1st atezolizumab-bevacizumab dose. Patients who underwent curative conversion had significantly longer survival than those who did not (P=0.024). Other factors associated with survival were male sex, Child-Pugh class A, and an objective response.

Conclusions: Despite the relatively large tumor size, successful curative conversion with MWA was achieved with first-line atezolizumab-bevacizumab in uHCC. However, data from prospective multicenter trials are required to determine whether this strategy is universally applicable.

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