Department of Cardiology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Department of Oncology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Curr Probl Cardiol. 2024 Jan;49(1 Pt C):102130. doi: 10.1016/j.cpcardiol.2023.102130. Epub 2023 Oct 18.
Recent advances in the treatment of breast cancer have resulted in improved overall cancer survival; however, cancer therapy related cardiac dysfunction is considered a major adverse effect of several chemotherapeutic agents, particularly anthracyclines. Hence, there is a need to develop proper cardioprotective strategies to limit myocardial injury following chemotherapy.
To evaluate the effect of statin therapy on prevention of anthracycline- induced cardiotoxicity in female patients with breast cancer.
The current study is a prospective, randomized, single-blind, placebo-controlled trial in which we enrolled a total of 110 female patients with newly diagnosed breast cancer who received anthracycline based chemotherapy. Patients were randomly assigned in 1:1 ratio into two groups, study group in which patients received 40 mg of oral atorvastatin and control group in which patients received placebo. A comprehensive echocardiographic examination was performed to all patients prior to receiving the chemotherapy and after 6 months, assessment of LV ejection fraction was done by 3D-echocardiography. All echocardiographers were blinded to all the patients' characteristics and assignment to either group.
The mean age of patients assigned to the control group was 49.8±10.51 years old, while patients assigned to the intervention group had mean age of 47.84± 9.16 years old, both the control group and the intervention group were similar in demographic data and baseline clinical characteristics. There was a highly significant difference between the two groups regarding both the absolute LVEF assessed by 3D- echocardiography at 6 months and the percentage of change compared to baseline values, patients assigned to the control group had mean LVEF of 52.92% at 6 months with percentage of change reaching -7.06%, while those assigned to the intervention group had mean LVEF reaching 56.22% at 6 months with a percentage of change reaching -3.64% (P-value: 0.008 and 0.004 for the absolute value and percentage of change respectively). There was a significant difference between the two groups regarding incidence of development of cancer therapy related cardiac dysfunction (CTRCD); defined as drop in LVEF more than 10% and to a value below 53% assessed by 3D echocardiography, among the control group 15 patients (30%) developed CTRCD after 6 months from starting Anthracyclines based chemotherapy, while, among the intervention group only 6 patients (12%) developed CTRCD. (P-value= 0.027) CONCLUSION: Prophylactic use of atorvastatin may prevent the development of cancer therapy related cardiac dysfunction in breast cancer patients receiving anthracycline based chemotherapy.
乳腺癌治疗的最新进展导致癌症总生存率提高;然而,癌症治疗相关的心脏功能障碍被认为是几种化疗药物的主要不良反应,尤其是蒽环类药物。因此,有必要制定适当的心脏保护策略,以限制化疗后心肌损伤。
评估他汀类药物治疗对预防女性乳腺癌患者蒽环类药物诱导的心脏毒性的作用。
本研究是一项前瞻性、随机、单盲、安慰剂对照试验,共纳入 110 例新诊断为乳腺癌的女性患者,均接受蒽环类药物化疗。患者按 1:1 比例随机分为两组,研究组患者口服阿托伐他汀 40mg,对照组患者服用安慰剂。所有患者在接受化疗前和 6 个月后均进行全面超声心动图检查,通过三维超声心动图评估左室射血分数。所有超声心动图检查者均对所有患者的特征和分组情况不知情。
对照组患者的平均年龄为 49.8±10.51 岁,而干预组患者的平均年龄为 47.84±9.16 岁,两组在人口统计学数据和基线临床特征方面相似。两组之间的绝对左室射血分数(通过三维超声心动图在 6 个月时评估)和与基线值相比的百分比变化均有显著差异,对照组患者在 6 个月时的平均左室射血分数为 52.92%,百分比变化达到-7.06%,而干预组患者在 6 个月时的平均左室射血分数达到 56.22%,百分比变化达到-3.64%(绝对值和百分比变化的 P 值分别为 0.008 和 0.004)。两组之间癌症治疗相关心脏功能障碍(CTRCD)的发生率也有显著差异;定义为通过三维超声心动图评估的左室射血分数下降超过 10%,并降至 53%以下,对照组中有 15 名患者(30%)在开始接受基于蒽环类药物的化疗后 6 个月时发生 CTRCD,而干预组中只有 6 名患者(12%)发生 CTRCD。(P 值=0.027)
预防性使用阿托伐他汀可预防接受蒽环类药物化疗的乳腺癌患者发生癌症治疗相关的心脏功能障碍。