Department of Oncology and Hematology, Division of Oncology, University Hospital of Modena, Via del Pozzo 71, Modena, Italy.
Department of Medical and Surgical Sciences - DIMEC, Alma Mater Studiorum-University of Bologna, Bologna, Italy.
Target Oncol. 2020 Dec;15(6):773-785. doi: 10.1007/s11523-020-00757-3.
Inflammation is a long-established hallmark of liver fibrosis and carcinogenesis. Eosinophils are emerging as crucial components of the inflammatory process influencing cancer development. The role of blood eosinophils in patients with hepatocellular carcinoma receiving systemic treatment is an unexplored field.
The objective of this study was to analyse the prognostic role of the baseline eosinophil count in patients with sorafenib-treated hepatocellular carcinoma.
A training cohort of 92 patients with advanced- or intermediate-stage sorafenib-treated hepatocellular carcinoma and two validation cohorts of 65 and 180 patients were analysed. Overall survival and progression-free survival in relation to baseline eosinophil counts were estimated by the Kaplan-Meier method. Univariate and multivariate analyses were performed.
A negative prognostic impact of low baseline eosinophil counts (< 50*10/L) was demonstrated in all cohorts (training cohort: hazard ratio = 50.1, 95% confidence interval 11.6-216.5, p < 0.0001 for low vs high eosinophil counts; first validation cohort: hazard ratio = 4.55, 95% confidence interval 1.24-16.65, p = 0.022; second validation cohort: hazard ratio = 3.21, 95% confidence interval 1.83-5.64, p < 0.0001). Moreover, low eosinophil counts had a negative prognostic role in patients progressing on or intolerant to sorafenib who received second-line regorafenib, but not capecitabine or best supportive care.
Our analysis identified baseline blood eosinophil counts as a new prognostic factor in patients with sorafenib-treated hepatocellular carcinoma. Concerning second-line therapies, eosinophil counts were associated with survival outcomes only in regorafenib-treated patients, suggesting a possible predictive role in this setting.
炎症是肝纤维化和癌变的一个长期确立的标志。嗜酸性粒细胞正在成为影响癌症发展的炎症过程中的关键组成部分。在接受系统治疗的肝细胞癌患者中,血液嗜酸性粒细胞的作用是一个尚未探索的领域。
本研究旨在分析索拉非尼治疗的肝细胞癌患者基线嗜酸性粒细胞计数的预后作用。
分析了 92 例接受索拉非尼治疗的晚期或中期肝细胞癌患者的训练队列,以及另外两个 65 例和 180 例患者的验证队列。通过 Kaplan-Meier 方法估计总生存期和无进展生存期与基线嗜酸性粒细胞计数的关系。进行了单因素和多因素分析。
在所有队列中(训练队列:危险比=50.1,95%置信区间 11.6-216.5,p<0.0001,低 vs 高嗜酸性粒细胞计数;第一验证队列:危险比=4.55,95%置信区间 1.24-16.65,p=0.022;第二验证队列:危险比=3.21,95%置信区间 1.83-5.64,p<0.0001),低基线嗜酸性粒细胞计数(<50*10/L)具有负预后作用。此外,在接受二线regorafenib 治疗的索拉非尼耐药或不耐受的患者中,低嗜酸性粒细胞计数具有负预后作用,但在接受 capecitabine 或最佳支持治疗的患者中没有。
我们的分析确定了基线血液嗜酸性粒细胞计数是索拉非尼治疗的肝细胞癌患者的一个新的预后因素。关于二线治疗,嗜酸性粒细胞计数仅与接受regorafenib 治疗的患者的生存结果相关,提示在这种情况下可能具有预测作用。