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吴慧, 孙丽娜, 潘璋驰, 施纯玫. T细胞活化与肿瘤负荷比对肝细胞癌患者抗PD-1免疫治疗反应的预测[J]. 肿瘤防治研究, 2023, 50(11): 1103-1108. DOI: 10.3971/j.issn.1000-8578.2023.23.0375
引用本文: 吴慧, 孙丽娜, 潘璋驰, 施纯玫. T细胞活化与肿瘤负荷比对肝细胞癌患者抗PD-1免疫治疗反应的预测[J]. 肿瘤防治研究, 2023, 50(11): 1103-1108. DOI: 10.3971/j.issn.1000-8578.2023.23.0375
WU Hui, SUN Lina, PAN Zhangchi, SHI Chunmei. Prediction of Responses of Patients with Hepatocellular Carcinoma to Anti-PD-1 Immunotherapy by T-cell Invigoration to Tumour Burden Ratio[J]. Cancer Research on Prevention and Treatment, 2023, 50(11): 1103-1108. DOI: 10.3971/j.issn.1000-8578.2023.23.0375
Citation: WU Hui, SUN Lina, PAN Zhangchi, SHI Chunmei. Prediction of Responses of Patients with Hepatocellular Carcinoma to Anti-PD-1 Immunotherapy by T-cell Invigoration to Tumour Burden Ratio[J]. Cancer Research on Prevention and Treatment, 2023, 50(11): 1103-1108. DOI: 10.3971/j.issn.1000-8578.2023.23.0375

T细胞活化与肿瘤负荷比对肝细胞癌患者抗PD-1免疫治疗反应的预测

Prediction of Responses of Patients with Hepatocellular Carcinoma to Anti-PD-1 Immunotherapy by T-cell Invigoration to Tumour Burden Ratio

  • 摘要:
    目的 探讨抗PD-1治疗后肝细胞癌患者外周血T细胞活化及其与肿瘤负荷比值对免疫治疗疗效的预测价值。
    方法 分析85例接受抗PD-1治疗的肝细胞癌(HCC)患者治疗前后的血清样本,通过流式细胞仪分析其外周血细胞亚群、T细胞活化,结合影像检查X-tile软件选取截断值,生存分析评估患者预后情况。
    结果 治疗周期中Ki-67+/PD-1+/CD8+ T细胞的最大倍数变化和通过影像确定的肿瘤负荷与免疫治疗的生存获益相关。在抗PD-1免疫治疗的第一个周期,T细胞Ki-67+/PD-1+/CD8+表达与肿瘤负荷比大于0.6与PFS和OS的改善相关(P < 0.05)。
    结论 免疫治疗后外周血T细胞的活化与肿瘤负荷比可能与肝细胞癌抗PD-1免疫治疗的临床疗效相关。

     

    Abstract:
    Objective To explore the predictive value of T cell activation in peripheral blood of patients with hepatocellular carcinoma(HCC) after anti PD-1 therapy and its ratio to tumor burden on the efficacy of immunotherapy.
    Methods Serum specimens were obtained before and after treatment from 85 patients with HCC who received anti-PD-1 treatment. Indicators such as cell subpopulations and T cell activation were detected by flow cytometry. Combined with imaging analysis, cutoff value was obtained by X-tile software. Survival analysis was used to evaluate patients' outcomes.
    Results The maximum fold change of Ki-67+/PD-1+/CD8+ T cells in treatment cycles and the tumor burden determined by imaging were associated with prognoses. The ratio of T cell Ki-67+/PD-1+/CD8+ expression to tumor burden ratio greater than 0.6 at the first cycle of anti-PD-1 immunotherapy was associated with improvements in progression-free survival and overall survival (P < 0.05).
    Conclusion The ratio of activationa in T cells in peripheral blood after immunotherapy to the tumor burden may be related to the clinical efficacy of anti-PD-1 immunotherapy for HCC.

     

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