Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.
Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.
ESMO Open. 2021 Feb;6(1):100020. doi: 10.1016/j.esmoop.2020.100020. Epub 2021 Jan 4.
The immunological inflammatory biomarkers for advanced hepatocellular carcinoma are unclear. We aimed to investigate the association of immunity and inflammatory status with treatment outcomes in patients with advanced hepatocellular carcinoma who received molecular-targeted agents as primary treatment.
We enrolled 728 consecutive patients with advanced hepatocellular carcinoma who received sorafenib (n = 554) or lenvatinib (n = 174) as primary treatment in Japan between May 2009 and June 2020. Changes in the neutrophil-to-lymphocyte ratio before and 1 month after treatment and their impact on survival were evaluated. The cut-off values of neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio for predicting overall and progression-free survival were calculated using receiver operating characteristic curves.
The neutrophil-to-lymphocyte ratio, but not the platelet-to-lymphocyte ratio, was an independent prognostic factor. Patients with decreased neutrophil-to-lymphocyte ratio survived significantly longer than patients with increased neutrophil-to-lymphocyte ratio (median overall survival: 14.7 versus 10.4 months, P = 0.0110). Among patients with a low pre-treatment neutrophil-to-lymphocyte ratio, the overall survival did not differ significantly between those with decreased and those with increased neutrophil-to-lymphocyte ratio after 1 month (median: 19.0 versus 14.8 months, P = 0.1498). However, among patients with high pre-treatment neutrophil-to-lymphocyte ratio, those whose neutrophil-to-lymphocyte ratio decreased after 1 month showed significantly longer survival than those whose neutrophil-to-lymphocyte ratio increased (median: 12.7 versus 5.5 months, P < 0.0001). The therapeutic effect was not correlated with pre-treatment neutrophil-to-lymphocyte ratio or platelet-to-lymphocyte ratio.
The neutrophil-to-lymphocyte ratio is a prognostic factor, along with liver function and tumor markers, in patients with advanced hepatocellular carcinoma who received molecular-targeted agents as primary treatment. Thus, the neutrophil-to-lymphocyte ratio could be a prognostic biomarker for advanced hepatocellular carcinoma primarily treated with immunotherapy.
目前尚不清楚晚期肝细胞癌的免疫炎症生物标志物。我们旨在研究接受分子靶向药物作为一线治疗的晚期肝细胞癌患者的免疫和炎症状态与治疗结果之间的关系。
我们纳入了 2009 年 5 月至 2020 年 6 月期间在日本接受索拉非尼(n=554)或仑伐替尼(n=174)作为一线治疗的 728 例连续晚期肝细胞癌患者。评估治疗前后中性粒细胞与淋巴细胞比值的变化及其对生存的影响。使用受试者工作特征曲线计算中性粒细胞与淋巴细胞比值和血小板与淋巴细胞比值的截断值,以预测总生存期和无进展生存期。
中性粒细胞与淋巴细胞比值是独立的预后因素,但血小板与淋巴细胞比值不是。与中性粒细胞与淋巴细胞比值升高的患者相比,中性粒细胞与淋巴细胞比值降低的患者生存时间显著延长(中位总生存期:14.7 个月比 10.4 个月,P=0.0110)。在治疗前中性粒细胞与淋巴细胞比值较低的患者中,治疗 1 个月后中性粒细胞与淋巴细胞比值降低的患者与中性粒细胞与淋巴细胞比值升高的患者之间的总生存期无显著差异(中位:19.0 个月比 14.8 个月,P=0.1498)。然而,在治疗前中性粒细胞与淋巴细胞比值较高的患者中,治疗 1 个月后中性粒细胞与淋巴细胞比值降低的患者的生存时间明显长于中性粒细胞与淋巴细胞比值升高的患者(中位:12.7 个月比 5.5 个月,P<0.0001)。治疗效果与治疗前中性粒细胞与淋巴细胞比值或血小板与淋巴细胞比值无关。
中性粒细胞与淋巴细胞比值与肝功能和肿瘤标志物一起是接受分子靶向药物作为一线治疗的晚期肝细胞癌患者的预后因素。因此,中性粒细胞与淋巴细胞比值可能是接受免疫治疗的晚期肝细胞癌的预后生物标志物。