Sui Xin, Jiang Leilei, Teng Huajing, Mi Lan, Li Bo, Shi Anhui, Yu Rong, Li Dongming, Dong Xin, Yang Dan, Yu Huiming, Wang Weihu
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Lymphoma, Peking University Cancer Hospital and Institute, Beijing, China.
Front Oncol. 2021 Feb 17;10:625911. doi: 10.3389/fonc.2020.625911. eCollection 2020.
To identify cytokines in plasma that may predict objective response and progression-free survival (PFS) in patients with locally advanced non-small cell lung cancer (NSCLC) treated with chemoradiotherapy.
From April 2016 to May 2017, thirty-one patients with locally advanced inoperable/unresectable NSCLC were included, and treated with concurrent chemoradiotherapy (CCRT). No immune checkpoint inhibitors were administered after CCRT. Plasma from each patient was collected before radiotherapy, and 25 cytokines in the plasma were measured by Luminex or U-PLEX assays. Logistic regression and COX regression were performed to identify the predictive factors for objective response and PFS, respectively. Kaplan-Meier survival analysis was used to compare the PFS between the groups.
High levels of IL-13 and TNF-α, and low levels of ICAM-1, IFN-γ, and soluble PD-L1 (sPD-L1) were significantly associated with objective response (0.05). High levels of IL-8, CCL5, and CXCL3 also showed a trend toward association with objective response (0.1). The combination of cytokines (IL-8 and ICAM-1, or TNF-α and sPD-L1) improved predictive accuracy. Univariate analysis identified IL-8 and ICAM-1 as potential markers to predict PFS. Multivariate analysis suggested that high level of IL-8 ( =0.010) and low level of ICAM-1 ( =0.011) correlated significantly with a longer PFS.
IL-8 and ICAM-1 in plasma have the potential to predict objective response and PFS in patients with locally advanced NSCLC underwent chemoradiotherapy.
鉴定血浆中的细胞因子,这些细胞因子可能预测接受放化疗的局部晚期非小细胞肺癌(NSCLC)患者的客观缓解和无进展生存期(PFS)。
纳入2016年4月至2017年5月期间31例局部晚期无法手术切除/不可切除的NSCLC患者,并行同步放化疗(CCRT)。CCRT后未给予免疫检查点抑制剂。放疗前采集每位患者的血浆,采用Luminex或U-PLEX检测法测定血浆中25种细胞因子。分别进行逻辑回归和COX回归以鉴定客观缓解和PFS的预测因素。采用Kaplan-Meier生存分析比较各组之间的PFS。
高水平的IL-13和TNF-α,以及低水平的ICAM-1、IFN-γ和可溶性PD-L1(sPD-L1)与客观缓解显著相关(P<0.05)。高水平的IL-8、CCL5和CXCL3也显示出与客观缓解相关的趋势(P=0.1)。细胞因子组合(IL-8和ICAM-1,或TNF-α和sPD-L1)提高了预测准确性。单因素分析确定IL-8和ICAM-1为预测PFS的潜在标志物。多因素分析表明,高水平的IL-8(P=0.010)和低水平的ICAM-1(P=0.011)与较长的PFS显著相关。
血浆中的IL-8和ICAM-1有可能预测接受放化疗的局部晚期NSCLC患者的客观缓解和PFS。