Du Tingting, Zou Jialin, Yang Yunying, Xie Honghui, Pang Hui, Zhuang Wenquan, Wang Shutong, Wei Guangyan
Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Department of Anorectal Surgery, Shenzhen Longgang Central Hospital, Shenzhen, China.
Front Oncol. 2025 Jan 10;14:1528138. doi: 10.3389/fonc.2024.1528138. eCollection 2024.
Elevated levels of carbohydrate antigen 19-9 (CA19-9) levels are known to worsen outcomes in various tumors by influencing immune responses. However, the role of CA19-9 in immunotherapy for hepatocellular carcinoma (HCC) remains poorly understood.
This study included 621 patients treated with anti-PD-1/PD-L1 treatment at the First Affiliated Hospital of Sun Yat-sen University from January 2017 to March 2023. During immunotherapy, CA19-9 levels were measured and classified as either elevated (≥35 U/mL) or normal (<35 U/mL) for clinical analysis.
Patients with elevated CA19-9 levels had significantly worse progression-free survival (PFS) and overall survival (OS). The 1-year and 2-year PFS rates were 53.3% and 29.1% in the normal CA19-9 group compared to 16.9% and 11.3% in the elevated group ( < 0.001). Similarly, the 1-year and 2-year OS rates were 90.5% and 75.5% in the normal group versus 64.0% and 36.5% in the elevated group ( < 0.001). Multivariate analysis confirmed CA19-9 was an independent prognostic factor for both PFS and OS. Bioinformatic analysis indicated that FUT3, a key gene in CA19-9 synthesis, correlated with increased macrophage infiltration. And increased M2 macrophage levels and reduced M1 macrophage levels were noted in HCC samples with elevated CA19-9 levels. Further experiments indicated blocking CA19-9 improved the efficacy of PD-1 treatment through inducing the M1-like polarization of macrophages.
Our findings demonstrate that elevated CA19-9 levels during immunotherapy are associated with poor survival outcomes in HCC patients. These findings highlight the crucial role of CA19-9 in shaping the tumor immune environment, particularly through its effect on macrophage polarization, and suggest that targeting CA19-9 may improve immunotherapy outcomes.
已知碳水化合物抗原19-9(CA19-9)水平升高会通过影响免疫反应使各种肿瘤的预后恶化。然而,CA19-9在肝细胞癌(HCC)免疫治疗中的作用仍知之甚少。
本研究纳入了2017年1月至2023年3月在中山大学附属第一医院接受抗PD-1/PD-L1治疗的621例患者。在免疫治疗期间,测量CA19-9水平,并将其分为升高(≥35 U/mL)或正常(<35 U/mL)进行临床分析。
CA19-9水平升高的患者无进展生存期(PFS)和总生存期(OS)明显更差。正常CA19-9组的1年和2年PFS率分别为53.3%和29.1%,而升高组分别为16.9%和11.3%(<0.001)。同样,正常组的1年和2年OS率分别为90.5%和75.5%,升高组分别为64.0%和36.5%(<0.001)。多因素分析证实CA19-9是PFS和OS的独立预后因素。生物信息学分析表明,CA19-9合成中的关键基因FUT3与巨噬细胞浸润增加相关。在CA19-9水平升高的HCC样本中,M2巨噬细胞水平升高,M1巨噬细胞水平降低。进一步实验表明,阻断CA19-9可通过诱导巨噬细胞向M1样极化来提高PD-1治疗的疗效。
我们的研究结果表明,免疫治疗期间CA19-9水平升高与HCC患者的不良生存结果相关。这些发现突出了CA19-9在塑造肿瘤免疫环境中的关键作用,特别是通过其对巨噬细胞极化的影响,并表明靶向CA19-9可能改善免疫治疗结果。