Allen Clint, Duffy Sonia, Teknos Theodoros, Islam Mozaffarul, Chen Zhong, Albert Paul S, Wolf Gregory, Van Waes Carter
Tumor Biology Section, Head and Neck Surgery Branch, National Institute of Deafness and Other Communication Disorders, NIH, Bethesda, Maryland 20892, USA.
Clin Cancer Res. 2007 Jun 1;13(11):3182-90. doi: 10.1158/1078-0432.CCR-06-3047.
Cytokines and growth factors modulated by transcription factor nuclear factor-kappaB and secreted by tumor and stromal cells are detectable in serum of patients with advanced cancers, including head and neck squamous cell carcinomas (SCC). Longitudinal changes in these serum factors could be early biomarkers of treatment response and survival.
Interleukin (IL)-6, IL-8, growth-related oncogene-1 (GRO-1), vascular endothelial growth factor (VEGF), and hepatocyte growth factor (HGF) concentrations were determined by Luminex multiplex assay using serum obtained at baseline and every 3 months in a prospective study of 30 patients with locally advanced (stage III/IV) oropharyngeal SCC receiving chemoradiation therapy. The relationship between baseline and direction of change in individual and multiple cytokines with cause-specific and disease-free survival was determined by Cox proportional hazards models and Kaplan-Meier survival analysis. Statistical analyses included adjustment for smoking status and response to chemoradiation.
Three-year cause-specific and disease-free survival was 74.4% and 68.9%. Nonsmoking history (P = 0.05) and higher baseline VEGF (P = 0.003) correlated with increased survival. Longitudinal increases in levels of individual factors predicted decreased cause-specific survival when adjusted for smoking history [IL-6: relative risk (RR), 3.8; 95% confidence interval (95% CI), 2.0-7.4; P = 0.004; IL-8: RR, 1.6; 95% CI, 1.2-2.2; P = 0.05; VEGF: RR, 3.0; 95% CI, 1.6-5.6; P = 0.01; HGF: RR, 2.9; 95% CI, 1.9-4.4; P = 0.02; and GRO-1: RR, 1.2; 95% CI, 1.1-1.3; P = 0.02]. For a given individual, large increases in the upper quartile for any three or more factors predicted poorer cause-specific survival compared with patients with two or fewer large increases in factor levels (P = 0.004).
Pretreatment VEGF levels and longitudinal change in IL-6, IL-8, VEGF, HGF, and GRO-1 may be useful as biomarkers for response and survival in patients with locally advanced oropharyngeal and head and neck SCC treated with chemoradiation.
在包括头颈部鳞状细胞癌(SCC)在内的晚期癌症患者血清中可检测到由转录因子核因子-κB调节并由肿瘤和基质细胞分泌的细胞因子和生长因子。这些血清因子的纵向变化可能是治疗反应和生存的早期生物标志物。
在一项对30例接受放化疗的局部晚期(III/IV期)口咽SCC患者的前瞻性研究中,使用基线时及每3个月采集的血清,通过Luminex多重检测法测定白细胞介素(IL)-6、IL-8、生长相关癌基因-1(GRO-1)、血管内皮生长因子(VEGF)和肝细胞生长因子(HGF)的浓度。通过Cox比例风险模型和Kaplan-Meier生存分析确定个体和多种细胞因子的基线与变化方向与特定病因生存率和无病生存率之间的关系。统计分析包括对吸烟状态和放化疗反应的调整。
三年特定病因生存率和无病生存率分别为74.4%和68.9%。无吸烟史(P = 0.05)和较高的基线VEGF(P = 0.003)与生存率增加相关。在调整吸烟史后,个体因子水平的纵向升高预示特定病因生存率降低[IL-6:相对风险(RR),3.8;95%置信区间(95%CI),2.0 - 7.4;P = 0.004;IL-8:RR,1.6;95%CI,1.2 - 2.2;P = 0.05;VEGF:RR,3.0;95%CI,1.6 - 5.6;P = 0.01;HGF:RR,2.9;95%CI,1.9 - 4.4;P = 0.02;GRO-1:RR,1.2;95%CI,1.1 - 1.3;P = 0.02]。对于给定个体,与因子水平有两次或更少大幅升高的患者相比,任何三种或更多因子的上四分位数大幅升高预示特定病因生存率较差(P = 0.004)。
预处理时的VEGF水平以及IL-6、IL-8、VEGF、HGF和GRO-1的纵向变化可能作为接受放化疗的局部晚期口咽及头颈部SCC患者反应和生存的生物标志物。