Division of Hepatobiliary and Pancreatic Oncology, Kanagawa Cancer Center, Yokohama, Japan.
Department of Gastroenterology, Internal Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Oncologist. 2023 Jul 5;28(7):e526-e533. doi: 10.1093/oncolo/oyad090.
Immune checkpoint inhibitors (ICIs) are effective for advanced hepatocellular carcinoma (HCC). However, there are few reports on the correlation between the clinical efficacy of ICIs and the development of immune-related adverse events (irAEs) in patients with HCC. The aim of this study was to investigate the association between irAE development and survival in patients with HCC treated with atezolizumab plus bevacizumab.
We enrolled 150 patients with advanced HCC treated with atezolizumab plus bevacizumab between October 2020 and October 2021 at 5 territorial institutions. We compared the efficacy of atezolizumab plus bevacizumab between patients who experienced irAEs (irAE group) and those who did not (non-irAE group).
Thirty-two patients (21.3%) developed irAEs of any grade. Grade 3/4 irAEs were observed in 9 patients (6.0%). The median progression-free survivals (PFS) in the irAE and non-irAE groups were 273 and 189 days, respectively (P = .055). The median overall survivals (OS) in the irAE and non-irAE groups were not reached and 458 days, respectively (P = .036). Grade 1/2 irAEs significantly prolonged PFS (P = .014) and OS (P = .003). Grade 1/2 irAEs were significantly associated with PFS (hazard ratio [HR], 0.339; 95% confidence interval [CI], 0.166-0.691; P = .003) and OS (HR, 0.086; 95% CI, 0.012-0.641; P = .017) on multivariate analysis.
The development of irAEs was associated with increased survival in a real-world population of patients with advanced HCC treated with atezolizumab plus bevacizumab. Grade 1/2 irAEs were strongly correlated with PFS and OS.
免疫检查点抑制剂(ICIs)对晚期肝细胞癌(HCC)有效。然而,关于 HCC 患者接受 ICI 治疗的临床疗效与免疫相关不良事件(irAE)发展之间的相关性的报道很少。本研究旨在探讨接受阿替利珠单抗联合贝伐珠单抗治疗的 HCC 患者 irAE 发展与生存之间的关系。
我们在 5 个地区机构招募了 2020 年 10 月至 2021 年 10 月期间接受阿替利珠单抗联合贝伐珠单抗治疗的 150 例晚期 HCC 患者。我们比较了发生 irAE(irAE 组)和未发生 irAE(非 irAE 组)的患者接受阿替利珠单抗联合贝伐珠单抗治疗的疗效。
32 例患者(21.3%)发生任何级别的 irAE。9 例患者(6.0%)发生 3/4 级 irAE。irAE 组和非 irAE 组的中位无进展生存期(PFS)分别为 273 天和 189 天(P=0.055)。irAE 组和非 irAE 组的中位总生存期(OS)分别为未达到和 458 天(P=0.036)。1/2 级 irAE 显著延长 PFS(P=0.014)和 OS(P=0.003)。多变量分析显示,1/2 级 irAE 与 PFS(风险比 [HR],0.339;95%置信区间 [CI],0.166-0.691;P=0.003)和 OS(HR,0.086;95%CI,0.012-0.641;P=0.017)显著相关。
在接受阿替利珠单抗联合贝伐珠单抗治疗的晚期 HCC 患者的真实世界人群中,irAE 的发生与生存的改善相关。1/2 级 irAE 与 PFS 和 OS 密切相关。