Clinical School of the Tianjin Second People's Hospital, Tianjin Medical University, Tianjin 300192, China.
Department of Hepatology, Tianjin Second People's Hospital, Tianjin 300192, China.
Cancer Biol Med. 2024 May 6;21(9):813-25. doi: 10.20892/j.issn.2095-3941.2024.0048.
To investigate the impact of metabolic dysfunction-associated steatotic liver disease (MASLD) on the efficacy of immune checkpoint inhibitor (ICI)-based therapy in patients with chronic hepatitis B (CHB)-related hepatocellular carcinoma (HCC).
A total of 155 patients with CHB-related HCC who received ICI-based therapy (in the Department of Hepatology, Tianjin Second People's Hospital and Department of Hepatobiliary Oncology, Tianjin Medical University Cancer Institute & Hospital) between April 2021 and December 2023 were evaluated. Patients were divided into two groups: MASLD concurrent with CHB [MASLD-CHB] ( = 38), and CHB ( = 117).
The median progression-free survival (PFS, 6.9 months 9.3 months; = 0.001), progressive disease (57.89% 37.61%; = 0.028), and disease control rate (42.11% 62.39%; = 0. 028) in the MASLD-CHB group were significantly worse than the CHB group. The median overall survival was not attained. The percentage of CD4+PD1+ (17. 56% 8.89%; < 0.001) and CD8+PD1+ T cells (10.50% 7.42%; = 0.005) in patient samples from the MASLD-CHB group were significantly higher than the CHB group. Concurrent MASLD [hazard ratio (HR) = 1.921; 95% CI, 1.138-3.245; = 0.015] and alpha-fetoprotein levels after 3 months of treatment (HR = 2.412; 95% CI, 1.360-4.279; = 0.003) were independent risk factors for PFS in all patients.
ICI-based therapy in patients with CHB-related HCC and concurrent MASLD resulted in poorer efficacy and shorter PFS compared to patients with CHB-related HCC alone.
探讨代谢相关脂肪性肝病(MASLD)对慢性乙型肝炎(CHB)相关肝细胞癌(HCC)患者接受免疫检查点抑制剂(ICI)治疗疗效的影响。
回顾性分析 2021 年 4 月至 2023 年 12 月在天津市第二人民医院肝病科和天津医科大学肿瘤医院肝胆肿瘤科接受 ICI 治疗的 155 例 CHB 相关 HCC 患者的临床资料,根据是否合并 MASLD 将患者分为 MASLD 合并 CHB 组(MASLD-CHB 组,n=38)和单纯 CHB 组(n=117)。
MASLD-CHB 组的中位无进展生存期(PFS)为 6.9 个月,明显短于单纯 CHB 组的 9.3 个月( =0.001);MASLD-CHB 组疾病进展率(57.89%)明显高于单纯 CHB 组(37.61%)( =0.028),疾病控制率(42.11%)明显低于单纯 CHB 组(62.39%)( =0.028)。两组患者中位总生存期均未达到。MASLD-CHB 组患者肿瘤组织中 CD4+PD1+T 细胞(17.56%)和 CD8+PD1+T 细胞(10.50%)的比例明显高于单纯 CHB 组(分别为 8.89%和 7.42%)(均<0.001)。多因素分析显示,合并 MASLD(HR=1.921,95%CI:1.138-3.245, =0.015)和治疗后 3 个月甲胎蛋白(AFP)水平(HR=2.412,95%CI:1.360-4.279, =0.003)是影响患者 PFS 的独立危险因素。
与单纯 CHB 相关 HCC 患者相比,CHB 相关 HCC 合并 MASLD 患者接受 ICI 治疗的疗效较差,PFS 更短。