Suppr超能文献

乐伐替尼治疗晚期肝细胞癌患者的真实世界经验。

Real-world experience of lenvatinib-based therapy in patients with advanced hepatocellular carcinoma.

作者信息

Wang Hung-Wei, Lai Hsueh-Chou, Su Wen-Pang, Kao Jung-Ta, Hsu Wei-Fan, Chen Hung-Yao, Chang Che-Wei, Huang Guan-Tarn, Peng Cheng-Yuan

机构信息

Center for Digestive Medicine, Department of Internal Medicine, China Medical University Hospital, Taichung.

School of Medicine, China Medical University, Taichung.

出版信息

J Gastrointest Oncol. 2024 Oct 31;15(5):2216-2229. doi: 10.21037/jgo-24-351. Epub 2024 Sep 24.

Abstract

BACKGROUND

Given the significant advancements in the management of hepatocellular carcinoma (HCC) and the emergence of novel treatment approaches, establishing reliable predictors has become crucial for optimizing patient selection and therapeutic sequencing in HCC. In this study, we aimed to investigate the prognostic factors and treatment efficacy associated with lenvatinib-based therapy.

METHODS

We retrospectively enrolled 53 patients receiving lenvatinib monotherapy, and 19 patients receiving lenvatinib plus immune checkpoint inhibitor combination therapy as their first-line systemic treatment for unresectable HCC at a single medical center. We employed univariate and multivariate Cox regression analyses to ascertain the factors influencing survival in these cohorts.

RESULTS

For lenvatinib monotherapy and the combination therapy, the objective response rates were 30.2% and 63.2%, respectively (P=0.03); the median progression-free survival (PFS) durations were 7 months [95% confidence interval (CI): 4.5-9.5] and 12 months (95% CI: 6.4-17.6), respectively (P=0.74); and the median overall survival (OS) was not reached in either group (P=0.93). Although patients receiving the combination therapy had a greater treatment response, no significant survival differences were observed between the lenvatinib monotherapy and combination therapy subgroups, even after inverse probability of treatment weighting (IPTW). Patients who received lenvatinib monotherapy could be stratified based on a combination of albumin-bilirubin (ALBI) grade (either grade 1 or 2a) and a neutrophil-lymphocyte ratio (NLR) of ≤5.8. Compared to the other subgroups combined, those who met both of these criteria exhibited PFS with a hazard ratio (HR) of 0.382 (95% CI: 0.168-0.871; P=0.02), corresponding to 11 and 5 months, respectively; and an OS (HR: 0.198, 95% CI: 0.043-0.920; P=0.04) of not reached versus 12 months, respectively, according to multivariate Cox regression analysis.

CONCLUSIONS

In our study cohort, there were no statistically significant differences observed in the survival rates between patients treated with lenvatinib monotherapy and those treated with a combination of lenvatinib and immunotherapy. The incorporation of ALBI grade and NLR facilitates the stratification of survival outcomes in patients with unresectable HCC undergoing lenvatinib monotherapy.

摘要

背景

鉴于肝细胞癌(HCC)管理方面的重大进展以及新治疗方法的出现,建立可靠的预测指标对于优化HCC患者的选择和治疗顺序至关重要。在本研究中,我们旨在探讨基于乐伐替尼治疗的预后因素和治疗效果。

方法

我们回顾性纳入了53例接受乐伐替尼单药治疗的患者,以及19例接受乐伐替尼联合免疫检查点抑制剂联合治疗作为不可切除HCC一线全身治疗的患者,这些患者均来自单一医疗中心。我们采用单因素和多因素Cox回归分析来确定影响这些队列生存的因素。

结果

对于乐伐替尼单药治疗和联合治疗,客观缓解率分别为30.2%和63.2%(P = 0.03);中位无进展生存期(PFS)分别为7个月[95%置信区间(CI):4.5 - 9.5]和12个月(95% CI:6.4 - 17.6)(P = 0.74);两组的中位总生存期(OS)均未达到(P = 0.93)。尽管接受联合治疗的患者治疗反应更大,但即使在进行治疗权重逆概率(IPTW)后,乐伐替尼单药治疗组和联合治疗组之间在生存率上也未观察到显著差异。接受乐伐替尼单药治疗的患者可根据白蛋白 - 胆红素(ALBI)分级(1级或2a级)和中性粒细胞 - 淋巴细胞比值(NLR)≤5.8进行分层。与其他组合亚组相比,同时符合这两个标准的患者的PFS危险比(HR)为0.382(95% CI:0.168 - 0.871;P = 0.02),分别对应11个月和5个月;根据多因素Cox回归分析,OS(HR:0.198,95% CI:0.043 - 0.920;P = 0.04),未达到与12个月。

结论

在我们的研究队列中,接受乐伐替尼单药治疗的患者与接受乐伐替尼和免疫治疗联合治疗的患者之间的生存率没有统计学上的显著差异。纳入ALBI分级和NLR有助于对接受乐伐替尼单药治疗的不可切除HCC患者的生存结果进行分层。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc03/11565097/ff0e90dd0324/jgo-15-05-2216-f1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验