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用于曲妥珠单抗相关心脏毒性一级预防的心脏保护剂:一项系统评价和荟萃分析

Cardioprotective Agents for the Primary Prevention of Trastuzumab-Associated Cardiotoxicity: A Systematic Review and Meta-Analysis.

作者信息

Goulas Kyriakos, Farmakis Dimitrios, Constantinidou Anastasia, Kadoglou Nikolaos P E

机构信息

Medical School, University of Cyprus, Nicosia 2029, Cyprus.

出版信息

Pharmaceuticals (Basel). 2023 Jul 9;16(7):983. doi: 10.3390/ph16070983.

Abstract

There are significant considerations about the prevention of cardiotoxicity caused by trastuzumab therapy in patients with breast cancer, leading to discontinuation. Recently, randomized controlled trials (RCTs) have evaluated the effects of early commitment of beta-blockers (BBs), angiotensin receptor blockers (ARBs) and angiotensin converting enzyme inhibitors (ACEIs) during trastuzumab chemotherapy in order to prevent the related cardiotoxicity. The present systematic review and meta-analysis of six RCTs included patients who have predominantly non-metastatic, HER2-positive, breast cancer and received trastuzumab as primary or adjuvant therapy. Those patients did not have any obvious cardiac dysfunction or any previous therapy with cardioprotective agent. We evaluated the efficacy of the aforementioned medications for primary prevention of cardiotoxicity, using random effects models. Any preventive treatment did not reduce cardiotoxicity occurrence compared to controls (Odds ratios (OR) = 0.92, 95% CI 0.54-1.56, = 0.75). Results were similar for ACEIs/ARBs and beta-blockers. Treatment with ACEIs/ARBs led to a slight, but significant, increase in LVEF in patients compared to the placebo group. Only two studies reported less likelihood of discontinuation of trastuzumab treatment. More adequately powered RCTs are needed to determine the efficacy of routine prophylactic therapy.

摘要

对于预防乳腺癌患者曲妥珠单抗治疗引起的心脏毒性,有一些重要的考虑因素,这可能导致治疗中断。最近,随机对照试验(RCT)评估了在曲妥珠单抗化疗期间早期使用β受体阻滞剂(BBs)、血管紧张素受体阻滞剂(ARBs)和血管紧张素转换酶抑制剂(ACEIs)预防相关心脏毒性的效果。本系统评价和对六项RCT的荟萃分析纳入了主要为非转移性、HER2阳性乳腺癌且接受曲妥珠单抗作为一线或辅助治疗的患者。这些患者没有明显的心脏功能障碍,也未曾接受过任何心脏保护剂治疗。我们使用随机效应模型评估了上述药物对心脏毒性一级预防的疗效。与对照组相比,任何预防性治疗均未降低心脏毒性的发生率(优势比(OR)=0.92,95%置信区间0.54 - 1.56,P = 0.75)。ACEIs/ARBs和β受体阻滞剂的结果相似。与安慰剂组相比,ACEIs/ARBs治疗使患者的左心室射血分数(LVEF)略有但显著增加。只有两项研究报告曲妥珠单抗治疗中断的可能性较小。需要更有充分说服力的RCT来确定常规预防性治疗的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac9/10383255/e25546683b7e/pharmaceuticals-16-00983-g001.jpg

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