Department of Hematopathology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China.
Department of Cardiology, The First Affiliated Hospital of Chongqing Medical University, 1 Youyi Road, Yuzhong, Chongqing, 400016, People's Republic of China.
Cardiovasc Toxicol. 2020 Feb;20(1):11-19. doi: 10.1007/s12012-019-09558-1.
Anthracycline-containing chemotherapy is commonly associated with irreversible cardiovascular toxicity. Beta blockers are currently recommended as first-line drugs for improving cardiac function. However, the effects of beta blocker on cardiac preservation and the duration of beta blocker intervention therapy in anthracycline-treated patients remain unclear. We systematically searched PubMed, Embase, and Cochrane for randomized controlled trials (published between January, 2000 and January, 2019) to determine the effectiveness of cardiac preservation of beta blocker in anthracycline-treated patients by accessing the change in left ventricular ejection fraction (LVEF) from pre- to post-chemotherapy. In addition, we conducted subgroup analysis based on the duration of beta blocker cardioprotective intervention and accumulative anthracycline dose. 11 RCTs were finally included. Beta blockers were associated with a significant smaller drop in the LVEF change (MD = 2.87, 95% CI 0.64 to 5.11, p = 0.01) compared to control groups. Besides, a subgroup analysis according to duration of beta blocker-based cardioprotective intervention (< 6 months vs = 6 months) showed significant subgroup difference in the LVEF change (MD = - 0.05, 95% CI - 0.91 to 0.81, p = 0.91; MD = 6.48, 95% CI 2.44 to 10.52, p = 0.002). An additional subgroup analysis according to accumulative anthracycline dose showed statistically significant difference in the LVEF change (MD = 4.61, 95% CI 0.78 to 8.45, p = 0.02) with moderate accumulative dose of anthracycline (doxorubicin between 250 and 400 mg/m). Prophylactic administration of beta blocker-based cardioprotective therapy may be beneficial to the myocardial preservation in anthracycline-treated patients. And long-term use of beta blocker appears to have a positive effect on ameliorating anthracycline-induced cardiomyopathy, especially in patients exposed to moderate accumulative doses of anthracycline.
蒽环类化疗药物常伴有不可逆的心血管毒性。β受体阻滞剂目前被推荐为改善心脏功能的一线药物。然而,β受体阻滞剂对心脏保护的作用以及在蒽环类药物治疗患者中的β受体阻滞剂干预治疗持续时间尚不清楚。我们系统地检索了 PubMed、Embase 和 Cochrane 中的随机对照试验(发表于 2000 年 1 月至 2019 年 1 月),通过评估化疗前后左心室射血分数(LVEF)的变化来确定β受体阻滞剂在蒽环类药物治疗患者中的心脏保护作用。此外,我们还根据β受体阻滞剂心脏保护干预的持续时间和累积蒽环类药物剂量进行了亚组分析。最终纳入了 11 项 RCT。与对照组相比,β受体阻滞剂组的 LVEF 变化下降幅度明显较小(MD=2.87,95%CI 0.64 至 5.11,p=0.01)。此外,根据β受体阻滞剂心脏保护干预的持续时间(<6 个月与=6 个月)进行的亚组分析显示,LVEF 变化的亚组差异有统计学意义(MD=-0.05,95%CI-0.91 至 0.81,p=0.91;MD=6.48,95%CI 2.44 至 10.52,p=0.002)。根据累积蒽环类药物剂量进行的进一步亚组分析显示,在累积蒽环类药物剂量适中(阿霉素 250 至 400mg/m)的患者中,LVEF 变化有统计学意义(MD=4.61,95%CI 0.78 至 4.45,p=0.02)。预防性使用基于β受体阻滞剂的心脏保护治疗可能有利于蒽环类药物治疗患者的心肌保护。长期使用β受体阻滞剂似乎对改善蒽环类药物引起的心肌病有积极作用,特别是在暴露于中等累积剂量蒽环类药物的患者中。