Zhang Feng, Wang Yong-Shuai, Li Shao-Peng, Zhao Bin, Huang Nan, Song Rui-Peng, Meng Fan-Zheng, Feng Zhi-Wen, Zhang Shen-Yu, Song Hua-Chuan, Chen Xiao-Peng, Liu Lian-Xin, Wang Ji-Zhou
Department of Hepatobiliary Surgery, Centre for Leading Medicine and Advanced Technologies of IHM, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, 230001, China.
Anhui Provincial Key Laboratory of Hepatopancreatobiliary Surgery, Hefei, Anhui, 230001, China.
J Gastroenterol. 2025 Apr;60(4):442-455. doi: 10.1007/s00535-024-02202-y. Epub 2024 Dec 23.
Immune checkpoint inhibitors (ICIs) are playing a significant role in the treatment of hepatocellular carcinoma (HCC). This study aims to explore the prognostic value of alpha-fetoprotein (AFP) and initial tumor shape irregularity in patients treated with ICIs.
In this retrospective, multi-center study, 296 HCC patients were randomly divided into the training set and the validation set in a 3:2 ratio. The training set was used to evaluate prognostic factors and to develop an easily applicable ATSI (AFP and Tumor Shape Irregularity) score, which was verified in the validation set.
The ATSI score was developed from two independent prognostic risk factors: baseline AFP ≥ 400 ng/ml (HR 1.73, 95% CI 1.01-2.96, P = 0.046) and initial tumor shape irregularity (HR 1.94, 95% CI 1.03-3.65, P = 0.041). The median overall survival (OS) was not reached (95% CI 28.20-NA) in patients who met no criteria (0 points), 25.8 months (95% CI 14.17-NA) in patients who met one criterion (1 point), and 17.03 months (95% CI 11.73-23.83) in patients who met two criteria (2 points) (P = 0.001). The median progression-free survival (PFS) was 10.83 months (95% CI 9.27-14.33) for 0 points, 8.03 months (95% CI 6.77-10.57) for 1 point, and 5.03 months (95% CI 3.83-9.67) for 2 points (P < 0.001). The validation set effectively verified these results (median OS, 37.43/24.27/14.03 months for 0/1/2 points, P = 0.028; median PFS, 13.93/8.30/4.90 months for 0/1/2 points, P < 0.001).
The ATSI score can effectively predict prognosis in HCC patients receiving ICIs.
免疫检查点抑制剂(ICIs)在肝细胞癌(HCC)治疗中发挥着重要作用。本研究旨在探讨甲胎蛋白(AFP)和初始肿瘤形状不规则性在接受ICIs治疗患者中的预后价值。
在这项回顾性多中心研究中,296例HCC患者按3:2比例随机分为训练集和验证集。训练集用于评估预后因素并制定易于应用的ATSI(AFP和肿瘤形状不规则性)评分,该评分在验证集中得到验证。
ATSI评分由两个独立的预后危险因素得出:基线AFP≥400 ng/ml(HR 1.73,95%CI 1.01 - 2.96,P = 0.046)和初始肿瘤形状不规则(HR 1.94,95%CI 1.03 - 3.65,P = 0.041)。符合无标准(0分)的患者中位总生存期(OS)未达到(95%CI 28.20 - NA),符合一项标准(1分)的患者为25.8个月(95%CI 14.17 - NA),符合两项标准(2分)的患者为17.03个月(95%CI 11.73 - 23.83)(P = 0.001)。0分患者的中位无进展生存期(PFS)为10.83个月(95%CI 9.27 - 14.33),1分患者为8.03个月(95%CI 6.77 - 10.57),2分患者为5.03个月(95%CI 3.83 - 9.67)(P < 0.001)。验证集有效验证了这些结果(0/1/2分的中位OS分别为37.43/24.27/14.03个月,P = 0.028;0/1/2分的中位PFS分别为13.93/8.30/4.90个月,P < 0.001)。
ATSI评分可有效预测接受ICIs治疗的HCC患者的预后。