Department of Medical Oncology, Thoracic Oncology Division, Catalan Institute of Oncology, Hospital Duran i Reynals, Avda Gran via, 199-203, L'Hospitalet, 08908, Barcelona, Spain.
Clinical Nutrition Unit, Catalan Institute of Oncology, Hospital Duran i Reynals, L'Hospitalet, Barcelona, Spain.
BMC Cancer. 2019 Feb 21;19(1):165. doi: 10.1186/s12885-019-5370-5.
Diabetes is related with increased cancer mortality across multiple cancer types. Its role in lung cancer mortality is still unclear. We aim to determine the prognostic value of fasting plasma glucose (FPG) and diabetes mellitus in patients with locally advanced non-small cell lung cancer (NSCLC) treated with concurrent chemoradiotherapy.
One-hundred seventy patients with stage III NSCLC received definitive concurrent chemoradiotherapy from 2010 to 2014. Clinico-pathological data and clinical outcome was retrospectively registered. Fifty-six patients (33%), met criteria for type 2 diabetes mellitus (T2DM) at baseline. The prognostic value of FPG and other clinical variables was assessed. Overall survival (OS) and progression-free survival (PFS) were estimated using the Kaplan-Meier method and Cox proportional models and log-rank test were used.
With a median follow-up of 36 months, median PFS was 8.0 months and median OS was 15.0 months in patients with FPG ≥7 mmol/L compared to 20 months (HR 1.13; 95% CI 1.07-1.19, p < 0.001) and 31 months (HR 1.09; 95% CI 1.04-1.15; p < 0.001) respectively, for patients with FPG < 7 mmol/L. In the multivariate analysis of the entire cohort adjusted by platinum compound and comorbidities, high levels of FPG as a continuous variable (HR 1.14; 95% CI 1.07-1.21; p < 0.001), the presence of comorbidity (HR 1.72; 95% CI 1.12-2.63; p = 0.012), and treatment with carboplatin (HR 1.95; 95% CI 1.26-2.99; p = 0.002) were independent predictors for shorter OS. In additional multivariate models considering non-diabetic patients as a reference group, diabetic patients with poor metabolic control (HbA1c > 8.5%) (HR 4.53; 95% CI 2.21-9.30; p < 0.001) and those receiving insulin (HR 3.22; 95% CI 1.90-5.46 p < 0.001) had significantly independent worse OS.
Baseline FPG level is an independent predictor of survival in our cohort of patients with locally advanced NSCLC treated with concurrent chemoradiotherapy. Studies in larger cohorts of patients are warranted to confirm this relevant association.
糖尿病与多种癌症类型的癌症死亡率增加有关。其在肺癌死亡率中的作用尚不清楚。我们旨在确定空腹血糖(FPG)和糖尿病在接受同步放化疗的局部晚期非小细胞肺癌(NSCLC)患者中的预后价值。
170 名 III 期 NSCLC 患者于 2010 年至 2014 年接受根治性同步放化疗。回顾性登记临床病理数据和临床结果。56 名患者(33%)在基线时符合 2 型糖尿病(T2DM)标准。评估 FPG 和其他临床变量的预后价值。使用 Kaplan-Meier 方法估计总生存期(OS)和无进展生存期(PFS),并使用 Cox 比例模型和对数秩检验进行分析。
中位随访 36 个月后,FPG≥7mmol/L 的患者的中位 PFS 为 8.0 个月,中位 OS 为 15.0 个月,而 FPG<7mmol/L 的患者分别为 20.0 个月(HR 1.13;95%CI 1.07-1.19,p<0.001)和 31.0 个月(HR 1.09;95%CI 1.04-1.15;p<0.001)。在整个队列的多变量分析中,通过铂类化合物和合并症进行调整,FPG 水平作为连续变量(HR 1.14;95%CI 1.07-1.21;p<0.001)、合并症的存在(HR 1.72;95%CI 1.12-2.63;p=0.012)和卡铂治疗(HR 1.95;95%CI 1.26-2.99;p=0.002)是 OS 较短的独立预测因素。在考虑非糖尿病患者作为参考组的其他多变量模型中,代谢控制不佳的糖尿病患者(HbA1c>8.5%)(HR 4.53;95%CI 2.21-9.30;p<0.001)和接受胰岛素治疗的患者(HR 3.22;95%CI 1.90-5.46;p<0.001)的 OS 明显更差。
在接受同步放化疗的局部晚期 NSCLC 患者中,基线 FPG 水平是生存的独立预测因子。需要更大的患者队列研究来证实这一相关关联。