Division of Hematology/Medical Oncology, Department of Medicine, Taichung Veterans General Hospital, 1650 Taiwan Boulevard Sect. 4, Taichung, Taiwan.
Department of Life Science, Tunghai University, 1727 Taiwan Boulevard Sect. 4, Taichung, Taiwan.
Clin Drug Investig. 2018 Jul;38(7):603-610. doi: 10.1007/s40261-018-0645-1.
Although anthracyclines are effective chemotherapeutic agents for treating B-cell lymphoma, adverse effects, such as bone marrow suppression and cardiotoxicity, limit their clinical application. We assessed whether anthracycline treatment also increases the risk for diabetes mellitus in patients with B-cell lymphoma.
Using data obtained from the Taiwanese National Health Insurance Research Database from 2004 to 2011, we compared overall survival and clinical features for B-cell lymphoma patients administered anthracyclines (n = 3147) and those not administered anthracyclines (n = 837). The impact of anthracycline treatment on diabetes risk was further investigated using a Gray's test and multivariate competing-risk regression models in a dose-dependent manner.
Anthracycline administration was associated with a higher incidence of diabetes (HR: 1.75; 95% CI 1.11-2.75; p = 0.0163) after adjustments for age, gender, cumulative dose of prednisolone, and co-morbidities. Cumulative anthracycline doses of 253-400 mg (HR: 2.35; 95% CI 1.41-3.91; p = 0.0010), 401-504 mg (HR: 2.26; 95% CI 1.26-4.05; p = 0.0063), and > 504 mg (HR: 2.29; 95% CI 1.25-4.18; p = 0.0072) increased the incidence density of diabetes in a dose-dependent manner (p = 0.0006). The annual alteration of adapted diabetes complications severity index score was not significantly different between B-cell lymphoma patients with or without anthracycline treatment (p = 0.4924).
Anthracycline therapy increases diabetes risk in a dose-dependent manner in B-cell lymphoma patients. Intensive blood glucose monitoring and control should be recommended for B-cell lymphoma patients receiving anthracycline treatment.
尽管蒽环类药物是治疗 B 细胞淋巴瘤的有效化疗药物,但骨髓抑制和心脏毒性等不良反应限制了其临床应用。我们评估了蒽环类药物治疗是否会增加 B 细胞淋巴瘤患者发生糖尿病的风险。
利用 2004 年至 2011 年台湾全民健康保险研究数据库的数据,我们比较了接受蒽环类药物治疗(n=3147)和未接受蒽环类药物治疗(n=837)的 B 细胞淋巴瘤患者的总生存率和临床特征。我们还使用 Gray 检验和多变量竞争风险回归模型,以剂量依赖性的方式进一步研究了蒽环类药物治疗对糖尿病风险的影响。
在调整年龄、性别、累积泼尼松剂量和合并症后,接受蒽环类药物治疗与糖尿病发病率升高相关(HR:1.75;95%CI 1.11-2.75;p=0.0163)。累积蒽环类药物剂量为 253-400mg(HR:2.35;95%CI 1.41-3.91;p=0.0010)、401-504mg(HR:2.26;95%CI 1.26-4.05;p=0.0063)和>504mg(HR:2.29;95%CI 1.25-4.18;p=0.0072)时,糖尿病的发生率密度呈剂量依赖性增加(p=0.0006)。有或没有蒽环类药物治疗的 B 细胞淋巴瘤患者之间,适应性糖尿病并发症严重程度指数评分的年变化无显著差异(p=0.4924)。
蒽环类药物治疗以剂量依赖性的方式增加了 B 细胞淋巴瘤患者发生糖尿病的风险。接受蒽环类药物治疗的 B 细胞淋巴瘤患者应推荐进行强化血糖监测和控制。