错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Alpha-fetoprotein combined with initial tumor shape irregularity in predicting the survival of patients with advanced hepatocellular carcinoma treated with immune-checkpoint inhibitors: a retrospective multi-center cohort study

  • Feng Zhang,
  • Yong-Shuai Wang,
  • Shao-Peng Li,
  • Bin Zhao,
  • Nan Huang,
  • Rui-Peng Song,
  • Fan-Zheng Meng,
  • Zhi-Wen Feng,
  • Shen-Yu Zhang,
  • Hua-Chuan Song,
  • Xiao-Peng Chen,
  • Lian-Xin Liu,
  • Ji-Zhou Wang

摘要

Background

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.

Methods

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.

Results

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).

Conclusions

The ATSI score can effectively predict prognosis in HCC patients receiving ICIs.