Postchemoradiotherapy systemic inflammation response index predicts treatment response and overall survival for patients with locally advanced nasopharyngeal cancer

医学 内科学 危险系数 置信区间 肿瘤科 优势比 比例危险模型 接收机工作特性 逻辑回归 阶段(地层学) 古生物学 生物
作者
Yueh‐Feng Lu,Chongsheng Wu,Wu‐Chia Lo,Yen‐Ling Chiu,Pei‐Wei Shueng,Chen‐Hsi Hsieh,Chen‐Xiong Hsu,Deng‐Yu Kuo,Pei‐Yu Hou,Li‐Jen Liao
出处
期刊:Journal of the Formosan Medical Association [Elsevier]
卷期号:122 (11): 1141-1149 被引量:2
标识
DOI:10.1016/j.jfma.2023.05.003
摘要

To explore the clinical utility of the systemic inflammation response index (SIRI) in the prediction of patients with poor treatment response to concurrent chemoradiotherapy (CCRT) in locally advanced nasopharyngeal cancer (NPC).A total of 167 stage III-IVB (AJCC 7th edition) nasopharyngeal cancer patients who received CCRT were retrospectively collected. The SIRI was calculated using the following formula: SIRI = neutrophil count × monocyte count/lymphocyte count (109/L). The optimal cutoff values of the SIRI for noncomplete response were determined by receiver operating characteristic curve analysis. Logistic regression analyses were performed to identify factors predictive of treatment response. We used Cox proportional hazards models to identify predictors of survival.Multivariate logistic regression showed that only the posttreatment SIRI was independently associated with treatment response in locally advanced NPC. A posttreatment SIRI≥1.15 was a risk factor for developing an incomplete response after CCRT (odds ratio 3.10, 95% confidence interval (CI): 1.22-9.08, p = 0.025). A posttreatment SIRI≥1.15 was also an independent negative predictor of progression-free survival (hazard ratio 2.38, 95% CI: 1.35-4.20, p = 0.003) and overall survival (hazard ratio 2.13, 95% CI: 1.15-3.96, p = 0.017).The posttreatment SIRI could be used to predict the treatment response and prognosis of locally advanced NPC.
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