Fiorella Guadagni, David Della-Morte, Patrizia Ferroni, San Raffaele Roma Open University, 00166 Rome, Italy.
World J Gastroenterol. 2017 Jul 28;23(28):5187-5195. doi: 10.3748/wjg.v23.i28.5187.
To investigate the possible predictive role of routinely used glycemic parameters for a first venous thromboembolism (VTE) episode in gastrointestinal (GI) cancer ambulatory patients - with or without clinically diagnosed type 2 diabetes (T2D) or obesity - treated with chemotherapy.
Pre-treatment fasting blood glucose, insulin, glycated hemoglobin (HbA) and homeostasis model of risk assessment (HOMA) were retrospectively evaluated in a cohort study of 342 GI cancer patients. Surgery was performed in 142 (42%) patients with primary cancer, 30 (21%) and 112 (79%) of whom received neoadjuvant and adjuvant therapies, respectively. First-line chemotherapy was administered in 200 (58%) patients with metastatic disease. The study outcome was defined as the occurrence of a first symptomatic or asymptomatic VTE episode during active treatment.
Impaired glucose tolerance (IGT) or T2D were diagnosed in 30% of GI cancer patients, while overweight/obesity had an incidence of 41%. VTE occurred in 9.4% of patients (7% of non-diabetic non-obese), especially in those with a high ECOG score ( = 0.025). No significant association was found between VTE incidence and T2D, obesity, different tumor types, metastatic disease, Khorana class of risk, or different anti-cancer drugs, although VTE rates were substantially higher in patients receiving bevacizumab (17% 8%, = 0.044). Conversely, all glucose metabolic indexes were associated with increased VTE risk at ROC analysis. Multivariate Cox proportional analyses confirmed that HOMA index (HR = 4.13, 95%CI: 1.63-10.5) or fasting blood glucose (HR = 3.56, 95%CI: 1.51-8.39) were independent predictors of VTE occurrence during chemotherapy.
The results here reported demonstrate that evaluating glucose metabolic asset may allow for VTE risk stratification in GI cancer, helping to identify chemotherapy-treated patients who might benefit from thromboprophylaxis. Further multicenter prospective studies involving a larger number of patients are presently needed.
探讨常规血糖参数对胃肠道(GI)癌症门诊患者首次静脉血栓栓塞(VTE)事件的预测作用-有或无临床诊断的 2 型糖尿病(T2D)或肥胖症-接受化疗。
在一项 342 名 GI 癌症患者的队列研究中,回顾性评估了治疗前空腹血糖、胰岛素、糖化血红蛋白(HbA)和风险评估的稳态模型(HOMA)。142 名(42%)原发性癌症患者接受了手术,其中 30 名(21%)和 112 名(79%)分别接受了新辅助和辅助治疗。200 名(58%)转移性疾病患者接受了一线化疗。研究结果定义为在积极治疗期间发生首次有症状或无症状的 VTE 事件。
30%的 GI 癌症患者被诊断为葡萄糖耐量受损(IGT)或 T2D,而超重/肥胖的发生率为 41%。9.4%的患者发生 VTE(非糖尿病非肥胖患者为 7%),尤其是 ECOG 评分较高的患者(= 0.025)。VTE 发生率与 T2D、肥胖、不同肿瘤类型、转移性疾病、Khorana 风险等级或不同抗癌药物之间无显著相关性,尽管接受贝伐单抗治疗的患者 VTE 发生率明显较高(17%比 8%,= 0.044)。相反,在 ROC 分析中,所有血糖代谢指标均与 VTE 风险增加相关。多变量 Cox 比例分析证实,HOMA 指数(HR = 4.13,95%CI:1.63-10.5)或空腹血糖(HR = 3.56,95%CI:1.51-8.39)是化疗期间 VTE 发生的独立预测因子。
本研究结果表明,评估血糖代谢状况可能有助于对 GI 癌症进行 VTE 风险分层,有助于识别可能受益于血栓预防的化疗患者。目前需要进行涉及更多患者的多中心前瞻性研究。