Anti-PD-1/L1 antibody plus anti-VEGF antibody vs. plus VEGFR-targeted TKI as first-line therapy for unresectable hepatocellular carcinoma: a network meta-analysis.

Q3 Medicine Exploration of targeted anti-tumor therapy Pub Date : 2024-01-01 Epub Date: 2024-06-17 DOI:10.37349/etat.2024.00236
Yiwen Zhou, Jingjing Li, Jieer Ying
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Abstract

Background: This article is based on our previous research, which was presented at the 2023 ASCO Annual Meeting I and published in Journal of Clinical Oncology as Conference Abstract (JCO. 2023;41:e16148. doi: 10.1200/JCO.2023.41.16_suppl.e16148). Both anti-programmed death 1/ligand-1 (PD-1/L1) antibody + anti-vascular endothelial growth factor (VEGF) antibody (A + A) and anti-PD-1/L1 antibody + VEGF receptor (VEGFR)-targeted tyrosine kinase inhibitor (A + T) are effective first-line therapies for unresectable hepatocellular carcinoma. However, there lacks evidence from head-to-head comparisons between these two treatments. We conducted a network meta-analysis on the efficacy and safety of them.

Methods: After a rigorous literature research, 6 phase III trials were identified for the final analysis, including IMbrave150, ORIENT-32, COSMIC-312, CARES-310, LEAP-002, and REFLECT. The experiments were classified into three groups: A + A, A + T, and intermediate reference group. The primary endpoint was overall survival (OS), and secondary endpoints included progression-free survival (PFS), objective response rate (ORR), and incidence of treatment-related adverse events (TRAEs). Hazard ratio (HR) with 95% confidence intervals (CI) for OS and PFS, odds ratio (OR) for ORR, and relative risk (RR) for all grade and grade ≥3 TRAEs were calculated. Under Bayesian framework, the meta-analysis was conducted using sorafenib as intermediate reference.

Results: With the rank probability of 96%, A + A showed the greatest reduction in the risk of death, without significant difference from A + T (HR: 0.82, 95% CI: 0.65-1.04). A + T showed the greatest effect in prolonging PFS and improving ORR with the rank probability of 77%, but there were no statistical differences with A + A. A + A was safer than A + T in terms of all grade of TRAEs (RR: 0.91, 95% CI: 0.82-1.00) and particularly in those grade ≥3 (RR: 0.65, 95% CI: 0.54-0.77).

Conclusions: A + A had the greatest probability of delivering the longest OS, while A + T was correlated with larger PFS benefits at the cost of a lower safety rate.

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抗PD-1/L1抗体加抗血管内皮生长因子抗体与加血管内皮生长因子受体靶向TKI作为不可切除肝细胞癌的一线疗法:一项网络荟萃分析。
背景:本文基于我们之前的研究,该研究已在 2023 年 ASCO 年会 I 上发表,并作为会议摘要发表在《临床肿瘤学杂志》上 (JCO. 2023;41:e16148. doi: 10.1200/JCO.2023.41.16_suppl.e16148)。抗程序性死亡1/配体-1(PD-1/L1)抗体+抗血管内皮生长因子(VEGF)抗体(A+A)和抗PD-1/L1抗体+VEGF受体(VEGFR)靶向酪氨酸激酶抑制剂(A+T)都是治疗不可切除肝细胞癌的有效一线疗法。然而,这两种疗法之间缺乏正面比较的证据。我们对它们的疗效和安全性进行了网络荟萃分析:经过严格的文献研究,最终确定了 6 项 III 期试验进行分析,包括 IMbrave150、ORIENT-32、COSMIC-312、CARES-310、LEAP-002 和 REFLECT。实验分为三组:A + A组、A + T组和中间参照组。主要终点是总生存期(OS),次要终点包括无进展生存期(PFS)、客观反应率(ORR)和治疗相关不良事件(TRAEs)的发生率。计算了OS和PFS的危险比(HR)及95%置信区间(CI)、ORR的几率比(OR)以及所有等级和等级≥3的TRAEs的相对风险(RR)。在贝叶斯框架下,以索拉非尼为中间参考进行了荟萃分析:在96%的秩概率下,A+A能最大程度地降低死亡风险,与A+T无显著差异(HR:0.82,95% CI:0.65-1.04)。就所有等级的TRAE而言,A + A比A + T更安全(RR:0.91,95% CI:0.82-1.00),尤其是≥3级的TRAE(RR:0.65,95% CI:0.54-0.77):结论:A+A最有可能提供最长的OS,而A+T与更大的PFS获益相关,但安全率较低。
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