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胃癌患者接受PD-1/PD-L1抑制剂治疗时胃免疫预后指数的预后价值

The Prognostic Value of Gastric Immune Prognostic Index in Gastric Cancer Patients Treated With PD-1/PD-L1 Inhibitors.

作者信息

Chen Li, Zhao Ruihu, Sun Hao, Huang Rong, Pan Hongming, Zuo Yanjiao, Zhang Lele, Xue Yingwei, Li Xingrui, Song Hongjiang

机构信息

Department of Thyroid and Breast Surgery, Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.

Department of Gastrointestinal Surgery, Harbin Medical University Cancer Hospital, Harbin Medical University, Harbin, China.

出版信息

Front Pharmacol. 2022 Jun 20;13:833584. doi: 10.3389/fphar.2022.833584. eCollection 2022.

Abstract

This study aimed to investigate the prognostic value of the gastric immune prognostic index (GIPI) in gastric cancer patients treated with programmed death 1/programmed death-ligand 1 (PD-1/PD-L1) inhibitors. This study was conducted to elucidate the role of GIPI using the data from 146 gastric cancer patients treated with PD-1/PD-L1 inhibitors between August 2016 and December 2020 in Harbin Medical University Cancer Hospital. The GIPI calculation was based on dNLR and LDH. Patients were categorized into three groups: 1) GIPI good (LDH ≤250 U/L and dNLR ≤3); 2) GIPI intermediate (LDH >250 U/L and NLR >3); 3) GIPI poor (LDH >250 U/L and dNLR >3). The correlations between GIPI and clinicopathologic characteristics were determined by the Chi-square test or the Fisher's exact test. The Kaplan-Meier analysis and log-rank test were used to calculate and compare progression-free survival (PFS) and overall survival (OS). The univariate and multivariate Cox proportional hazards regression model was used to detect prognostic and predictive factors of PFS and OS. 146 patients treated with PD-1/PD-L1 inhibitors were included in this study, of which, 72.6% were GIPI good, 23.3% were GIPI intermediate, and 4.1% were GIPI poor. The GIPI was associated with the common blood parameters, including neutrophils and lymphocytes. The multivariate analysis showed that platelet, TNM stage, and treatment were the independent prognostic factors for PFS and OS. Patients with GIPI intermediate/poor were associated with shorter PFS (median: 24.63 vs. 32.50 months; = 0.078) and OS (median: 28.37 months vs. not reached; = 0.033) than those with GIPI good. GIPI intermediate/poor was correlated with shorter PFS and OS than GIPI good, especially in subgroups of patients with ICI treatment and patients with PD-1/PD-L1 positive status. The GIPI correlated with poor outcomes for PD-1/PD-L1 expression status and may be useful for identifying gastric cancer patients who are unlikely to benefit from treatment.

摘要

本研究旨在探讨胃免疫预后指数(GIPI)在接受程序性死亡蛋白1/程序性死亡配体1(PD-1/PD-L1)抑制剂治疗的胃癌患者中的预后价值。本研究利用2016年8月至2020年12月期间在哈尔滨医科大学附属肿瘤医院接受PD-1/PD-L1抑制剂治疗的146例胃癌患者的数据,以阐明GIPI的作用。GIPI的计算基于dNLR和LDH。患者被分为三组:1)GIPI良好(LDH≤250 U/L且dNLR≤3);2)GIPI中等(LDH>250 U/L且NLR>3);3)GIPI较差(LDH>250 U/L且dNLR>3)。通过卡方检验或Fisher精确检验确定GIPI与临床病理特征之间的相关性。采用Kaplan-Meier分析和对数秩检验来计算和比较无进展生存期(PFS)和总生存期(OS)。单因素和多因素Cox比例风险回归模型用于检测PFS和OS的预后及预测因素。本研究纳入了146例接受PD-1/PD-L1抑制剂治疗的患者,其中72.6%为GIPI良好,23.3%为GIPI中等,4.1%为GIPI较差。GIPI与常见血液参数相关,包括中性粒细胞和淋巴细胞。多因素分析显示,血小板、TNM分期和治疗是PFS和OS的独立预后因素。与GIPI良好的患者相比,GIPI中等/较差的患者PFS(中位数:24.63个月对32.50个月;P = 0.078)和OS(中位数:28.37个月对未达到;P = 0.033)较短。GIPI中等/较差与PFS和OS较短相关,而GIPI良好则不然,尤其是在接受免疫检查点抑制剂(ICI)治疗的患者亚组和PD-1/PD-L1阳性状态的患者中。GIPI与PD-1/PD-L1表达状态的不良预后相关,可能有助于识别不太可能从治疗中获益的胃癌患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79a0/9251404/c036a063d4e7/fphar-13-833584-g001.jpg

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