Hanai Nobuhiro, Sawabe Michi, Kimura Takahiro, Suzuki Hidenori, Ozawa Taijiro, Hirakawa Hitoshi, Fukuda Yujiro, Hasegawa Yasuhisa
Department of Head and Neck Surgery, Aichi Cancer Center Hospital, Aichi, Japan.
Department of Otorhinolaryngology, Head and Neck Surgery, Nagoya City University Graduate School of Medical Sciences, Aichi, Japan.
Oncotarget. 2018 Dec 11;9(97):37008-37016. doi: 10.18632/oncotarget.26438.
There is increasing evidence that the inflammatory indices of modified Glasgow prognostic score (mGPS) and high-sensitivity mGPS (HS-mGPS) play important roles in predicting the survival in many cancer; however, evidence supporting such an association in head and neck cancer (HNC) is scarce.
We evaluated the impact of the mGPS and HS-mGPS on the overall survival (OS) in 129 patients with HNC treated at Aichi Cancer Center Central Hospital from 2012-2013. The mGPS was calculated as follows: mGPS of 0, C-reactive protein (CRP) ≤1.0 mg/dl; 1, CRP >1.0 mg/dl; 2, CRP>1.0 mg/dl and albumin <3.5 mg/dl. Regarding the HS-mGPS, the CRP threshold level was set as 0.3 mg/dl. Hazard ratios (HRs) and 95% confidence intervals (95% CIs) were estimated by Cox proportional hazard models after adjusting for potential confounders.
The prognosis of HNC worsened significantly as both the mGPS and HS-mGPS increased in a univariate analysis. After adjusting for covariates, the HS-mGPS was significantly associated with the OS (adjusted HR for HS-mGPS of 2 compared to an HS-mGPS of 0 [HR] 3.14 [95% CI: 1.23-8.07], P < 0.001), while the mGPS was suggested to be associated with the survival (HR 2.37 [95% CI:0.89-6.33], P = 0.145). Even after stratification by clinical covariates, these associations persisted.
We conclude that the HS-mGPS is useful as an independent prognostic factor in HNC.
越来越多的证据表明,改良格拉斯哥预后评分(mGPS)和高敏mGPS(HS-mGPS)的炎症指标在预测多种癌症的生存率方面发挥着重要作用;然而,支持头颈部癌(HNC)存在这种关联的证据却很少。
我们评估了mGPS和HS-mGPS对2012年至2013年在爱知县癌症中心中央医院接受治疗的129例HNC患者总生存期(OS)的影响。mGPS的计算方法如下:mGPS为0时,C反应蛋白(CRP)≤1.0mg/dl;为1时,CRP>1.0mg/dl;为2时,CRP>1.0mg/dl且白蛋白<3.5mg/dl。对于HS-mGPS,CRP阈值设定为0.3mg/dl。在调整潜在混杂因素后,通过Cox比例风险模型估计风险比(HRs)和95%置信区间(95% CIs)。
在单因素分析中,随着mGPS和HS-mGPS的升高,HNC的预后显著恶化。在调整协变量后,HS-mGPS与OS显著相关(HS-mGPS为2与HS-mGPS为0相比的调整后HR为3.14 [95% CI:1.23 - 8.07],P < 0.001),而mGPS提示与生存率相关(HR为2.37 [95% CI:0.89 - 6.33],P = 0.145)。即使按临床协变量分层后,这些关联仍然存在。
我们得出结论,HS-mGPS可作为HNC的独立预后因素。