Tang Mingyang, Liu Tao, Zhang Yukun, Ding Jun
Health Science Center, Hubei Minzu University, Enshi Hubei, 445000, China.
Hepatobiliary Pancreatic Spleen Surgery, The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, No. 158 Wuyang Avenue, Wuyangba Street, Enshi Hubei, Hubei Province, 445000, China.
Eur J Clin Pharmacol. 2025 Jun;81(6):815-830. doi: 10.1007/s00228-025-03829-3. Epub 2025 Apr 2.
The efficacy and safety of pembrolizumab in treating advanced hepatocellular carcinoma (HCC) are inconsistent across studies. This study sheds light on the efficacy and safety of pembrolizumab in advanced HCC patients.
Several databases were comprehensively searched up to January 13, 2025, to identify studies assessing pembrolizumab for advanced HCC. Outcome indicators included overall survival (OS), progression-free survival (PFS), objective response rate (ORR), rash, adverse events (AEs), and severe adverse events (SAEs). Pooled effects were estimated through hazard ratios (HRs) and odds ratios (ORs) with 95% confidence intervals (CIs). R 4.4.1. was employed for statistical analyses.
Twenty-two studies involving 2964 patients were encompassed. Meta-analysis indicated that pembrolizumab demonstrated an ORR of 28% in single-arm analyses. Pembrolizumab significantly improved ORR in comparison to placebo (OR = 2.57, 95% CI: 1.32-5.03) but showed no significant advantage over nivolumab. Pembrolizumab markedly enhanced PFS (HR = 0.76, 95% CI: 0.69-0.85) and OS (HR = 0.78, 95% CI: 0.70-0.88) compared to placebo, but no significant differences were observed when compared to nivolumab. Pembrolizumab significantly raised the risk of rash in comparison to placebo (OR = 2.27, 95% CI: 1.55-3.31) but showed no significant difference versus nivolumab. The pembrolizumab group showed a higher incidence of AEs (OR = 1.94, 95% CI: 1.42-2.64) and SAEs (OR = 2.10, 95% CI: 1.04-4.25) than the placebo group, with no significant difference between pembrolizumab and nivolumab.
This study proves that pembrolizumab may have promising therapeutic effects in patients with advanced HCC, although no clear advantage over nivolumab was observed. The occurrence of AEs warrants attention in clinical practice.
帕博利珠单抗治疗晚期肝细胞癌(HCC)的疗效和安全性在各项研究中并不一致。本研究揭示了帕博利珠单抗在晚期HCC患者中的疗效和安全性。
全面检索了截至2025年1月13日的多个数据库,以确定评估帕博利珠单抗治疗晚期HCC的研究。结局指标包括总生存期(OS)、无进展生存期(PFS)、客观缓解率(ORR)、皮疹、不良事件(AE)和严重不良事件(SAE)。通过风险比(HR)和比值比(OR)及95%置信区间(CI)估计合并效应。使用R 4.4.1进行统计分析。
纳入了22项涉及2964例患者的研究。荟萃分析表明,在单臂分析中,帕博利珠单抗的客观缓解率为28%。与安慰剂相比,帕博利珠单抗显著提高了客观缓解率(OR = 2.57,95% CI:1.32 - 5.03),但与纳武利尤单抗相比无显著优势。与安慰剂相比,帕博利珠单抗显著提高了无进展生存期(HR = 0.76,95% CI:0.69 - 0.85)和总生存期(HR = 0.78,95% CI:0.70 - 0.88),但与纳武利尤单抗相比未观察到显著差异。与安慰剂相比,帕博利珠单抗显著增加了皮疹风险(OR = 2.27,95% CI:1.55 - 3.31),但与纳武利尤单抗相比无显著差异。帕博利珠单抗组的不良事件(OR = 1.94,95% CI:1.42 - 2.64)和严重不良事件(OR = 2.10,95% CI:1.04 - 4.25)发生率高于安慰剂组,帕博利珠单抗与纳武利尤单抗之间无显著差异。
本研究证明,帕博利珠单抗在晚期HCC患者中可能具有良好的治疗效果,尽管未观察到其相对于纳武利尤单抗有明显优势。在临床实践中,不良事件的发生值得关注。