University of Pittsburgh School of Medicine.
Department of Radiation Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA.
Am J Clin Oncol. 2019 Sep;42(9):692-697. doi: 10.1097/COC.0000000000000580.
Studies have consistently identified an increased risk of pancreatic cancer in diabetics, yet the role hyperglycemia may play in predicting prognosis is less clear. This work aims to evaluate the impact of glycemic state and antidiabetics on outcomes after systemic and local treatment for locoregionally advanced pancreatic cancer.
This retrospective study consisted of 303 patients with newly diagnosed advanced-stage pancreatic cancer treated from 2004 to 2014. Kaplan-Meier survival analysis method was used to estimate time to event for overall survival, distant metastasis, and locoregional control. Blood glucose values (n=8599) were assessed both as continuous and categorical variables in univariate and multivariable Cox proportional hazard regression models to estimate hazard ratios (HRs) and identify independent prognostic factors. A 6-month conditional landmark analysis excluding patients with <6 months follow-up or survival was conducted.
Median follow-up and survival was 18.1 and 18.4 months, respectively. On univariate analysis, maximum pretreatment glucose value was associated with reduced overall survival (HR 1.005, P=0.023) and locoregional control (HR 1.001, P=0.001). A pretreatment glucose value ≥200 mg/dL was associated with increased mortality in multivariable analysis (adjusted HR 1.01, P=0.015). After conditional analysis, glucose ≥200 mg/dL before local treatment was associated with reduced overall survival (adjusted HR 1.562; 95% confidence interval [CI], 1.16-2.11; P=0.003).
Elevated blood glucose before treatment of locoregionally advanced pancreatic cancer was associated with poorer outcomes. These findings should be incorporated in future clinical trial design.
研究一致表明,糖尿病患者患胰腺癌的风险增加,但高血糖在预测预后方面的作用尚不清楚。本研究旨在评估血糖状态和降糖药物在局部晚期胰腺癌全身和局部治疗后的结局中的作用。
本回顾性研究纳入了 2004 年至 2014 年期间新诊断为局部晚期胰腺癌的 303 例患者。采用 Kaplan-Meier 生存分析法估计总生存、远处转移和局部区域控制的时间事件。在单变量和多变量 Cox 比例风险回归模型中,将血糖值(n=8599)评估为连续和分类变量,以估计风险比(HR)并确定独立的预后因素。对 6 个月的条件性地标分析进行了排除随访或生存时间<6 个月的患者。
中位随访和生存时间分别为 18.1 个月和 18.4 个月。单因素分析显示,最大预处理血糖值与总生存(HR 1.005,P=0.023)和局部区域控制(HR 1.001,P=0.001)降低相关。预处理血糖值≥200mg/dL 与多变量分析中的死亡率增加相关(调整后的 HR 1.01,P=0.015)。经过条件分析,局部治疗前血糖≥200mg/dL 与总生存降低相关(调整后的 HR 1.562;95%置信区间[CI],1.16-2.11;P=0.003)。
局部晚期胰腺癌治疗前血糖升高与预后不良相关。这些发现应纳入未来的临床试验设计中。