Nam Heechul, Lee Jaejun, Han Ji Won, Lee Soon Kyu, Yang Hyun, Lee Hae Lim, Sung Pil Soo, Kim Hee Yeon, Kim Seok-Hwan, Song Myeong Jun, Kwon Jung-Hyun, Kim Chang Wook, Nam Soon Woo, Bae Si Hyun, Choi Jong Young, Yoon Seung Kew, Jang Jeong Won
The Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Division of Gastroenterology and Hepatology, Department of Internal Medicine, College of Medicine, Uijeongbu St. Mary's Hospital, The Catholic University of Korea, Seoul, Republic of Korea.
Liver Cancer. 2023 Dec 21;13(4):413-425. doi: 10.1159/000535839. eCollection 2024 Aug.
Despite the emergence of atezolizumab and bevacizumab (A + B) as standard first-line systemic therapy for unresectable hepatocellular carcinoma (HCC), a comprehensive understanding of the clinical significance of immune-related adverse events (irAEs) remains limited. We aimed to assess the impact of irAEs on patients with HCC undergoing A + B treatment.
This multicentre retrospective study included consecutive patients with HCC who were treated with the A + B regimen from September 2020 to December 2022. Patients were categorized into three groups based on the severity of irAEs, ranging from those without any experience of irAEs to those with severe irAEs.
This study included 150 patients with HCC, with a mean age of 63.3 years. Among them, 93.3% of patients were classified as Barcelona Clinic Liver Cancer stage C, 52.0% had portal vein tumour thrombosis (PVTT), and 60.7% extrahepatic spread. Patients were classified as follows: group 1 ( = 84) had no irAEs, group 2 ( = 37) had mild irAEs (grade 1-2), and group 3 ( = 29) had severe irAEs (grade ≥3). The median overall survival (OS), progression-free survival (PFS), and time-to-treatment discontinuation (TTD) were 13.6, 5.7, and 3.6 months, respectively. Group 2 demonstrated significantly superior OS compared to group 1 (9.5 months) and group 3 (5.6 months), with a median OS of 23.0 months ( < 0.001). Furthermore, group 2 demonstrated significantly better outcomes in terms of PFS and TTD compared to both group 1 and group 3 ( < 0.001 for both). Multivariate analysis identified mild irAEs (hazard ratio [HR], 0.353; = 0.010), ALBI grade 1 (HR, 0.389; = 0.006), Child-Pugh class A (HR, 0.338; = 0.002), and the absence of PVTT (HR, 0.556; = 0.043) as independent predictors of better OS.
Our study highlights the significant impact of irAE severity on the outcomes of patients with HCC receiving A + B. Notably, the occurrence of mild irAEs was independently associated with favourable survival, suggesting their potential role as surrogate indicators of HCC prognosis.
尽管阿替利珠单抗和贝伐珠单抗(A+B)已成为不可切除肝细胞癌(HCC)的标准一线全身治疗方案,但对免疫相关不良事件(irAE)临床意义的全面理解仍然有限。我们旨在评估irAE对接受A+B治疗的HCC患者的影响。
这项多中心回顾性研究纳入了2020年9月至2022年12月期间连续接受A+B方案治疗的HCC患者。根据irAE的严重程度,患者被分为三组,从无irAE经历的患者到有严重irAE的患者。
本研究纳入了150例HCC患者,平均年龄为63.3岁。其中,93.3%的患者被归类为巴塞罗那临床肝癌C期,52.0%有门静脉肿瘤血栓形成(PVTT),60.7%有肝外转移。患者分类如下:第1组(n=84)无irAE,第2组(n=37)有轻度irAE(1-2级),第3组(n=29)有严重irAE(≥3级)。中位总生存期(OS)、无进展生存期(PFS)和治疗中断时间(TTD)分别为13.6个月、5.7个月和3.6个月。第2组的OS明显优于第1组(9.5个月)和第3组(5.6个月),中位OS为23.0个月(P<0.001)。此外,第2组在PFS和TTD方面的结果明显优于第1组和第3组(两者均P<0.001)。多变量分析确定轻度irAE(风险比[HR],0.353;P=0.010)、ALBI 1级(HR,0.389;P=0.006)、Child-Pugh A级(HR,0.338;P=0.002)以及无PVTT(HR,0.556;P=0.043)是更好OS的独立预测因素。
我们的研究强调了irAE严重程度对接受A+B治疗的HCC患者结局的重大影响。值得注意的是,轻度irAE的发生与良好的生存率独立相关,表明它们可能作为HCC预后的替代指标。