Efficacy and safety of atezolizumab plus bevacizumab in Korean patients with advanced hepatocellular carcinoma

Efficacy and safety of atezolizumab plus bevacizumab in Korean patients with advanced hepatocellular carcinoma
复制标题

DOI:
10.1111/liv.15102
复制
发表时间:
2021-11-29
影响因子:
6.7
通讯作者:
Lim, Ho Yeong
Lim, Ho Yeong
中科院分区:
医学2区
文献类型:
--
作者:
Cheon, Jaekyung;Yoo, Changhoon;Lim, Ho Yeong

文献摘要

被引文献

相似文献

Atezolizumab联合贝伐单抗(Ate/Bev)在晚期肝细胞癌(HCC)患者中的III期临床试验已证实有效性和安全性。需要进一步评价,以研究Ate/Bev在真实的环境中的安全性和有效性。方法采用多中心回顾性分析。2020年5月至2021年2月期间,来自11家机构的138名患者接受了Ate/Bev作为晚期HCC的一线治疗。我们排除了Child-Pugh B或C和BCLC D分期的患者,其余121例患者纳入本分析。结果按RECIST1.1标准评价,客观缓解率和疾病控制率分别为24.0%和76.0%。中位随访时间为5.9个月(95%置信区间[CI],5.4-6.4),中位无进展生存期(PFS)为6.5个月(95% CI,4.1-9.0),未达到中位总生存期(OS)(95% CI,不可用)。最常见的3-4级不良事件是天冬氨酸转氨酶升高(10.7%)。在多变量分析中,AFP升高(P = 0.037)、基线嗜中性粒细胞/淋巴细胞比值(NLR)>= 5(P = 0.023)和疾病稳定或疾病进展的最佳缓解(P = 0.019)与PFS恶化显著相关。大血管侵犯(P = .048)和基线NLR >= 5(P < .001)与OS恶化显著相关。结论Ate/Bev在韩国晚期HCC患者中显示了真实的疗效和安全性,与III期试验的结果一致。考虑到在NLR升高的患者中Ate/Bev的不利生存结局,需要在该组中仔细评估治疗反应。
Background & Aims Atezolizumab plus bevacizumab (Ate/Bev) has demonstrated efficacy and safety in patients with advanced hepatocellular carcinoma (HCC) in the phase III trial. Further evaluation is necessary to investigate the safety and efficacy of Ate/Bev in real settings. Methods This was a multicentre retrospective analysis. Between May 2020 and February 2021, 138 patients received Ate/Bev as first-line treatment for advanced HCC from 11 institutions. We excluded patients with Child-Pugh B or C and BCLC D stage, and the remaining 121 patients were included in this analysis. Results According to RECIST 1.1, the objective response and disease control rates were 24.0% and 76.0%. The median follow-up duration was 5.9 months (95% confidence interval [CI], 5.4-6.4), the median progression-free survival (PFS) was 6.5 months (95% CI, 4.1-9.0), and median overall survival (OS) was not reached (95% CI, not available). The most frequent grade 3-4 adverse event was aspartate aminotransferase elevation (10.7%). In the multivariate analyses, AFP increase (P = .037), baseline neutrophil-to-lymphocyte ratio (NLR) >= 5 (P = .023), and best response to stable disease or progressive disease (P = .019) were significantly associated with worse PFS. Macrovascular invasion (P = .048) and baseline NLR >= 5 (P < .001) were significantly associated with worse OS. Conclusions Ate/Bev showed real-life efficacy and safety in Korean patients with advanced HCC, in line with results from phase III trial. Considering unfavourable survival outcomes of Ate/Bev in patients with elevated NLR, careful assessment of treatment response needs to be performed in this group.