Murg Sergiu Ioan, Matiș Loredana, Moldovan Andrada Florina, Schwarz-Madar Andrada Florina, Trifan Daniela Florina, Ghitea Timea Claudia, Popescu Mircea Ioachim
Doctoral School, Faculty of Medicine and Pharmacy, University of Oradea, 410068 Oradea, Romania.
Department of Clinical Discipline, Faculty of Medicine and Pharmacy, University of Oradea, 410068 Oradea, Romania.
Cancers (Basel). 2024 Dec 23;16(24):4281. doi: 10.3390/cancers16244281.
BACKGROUND/OBJECTIVES: Cardio-oncology has become essential in addressing cardiovascular complications from cancer therapies. While advancements in treatments have improved survival rates, they also increase cardiovascular risks. This study evaluates the cardiotoxic effects of cytostatic treatments, examining the relationship between tumor characteristics, such as histopathology and TNM classification, and cardiovascular complications, aiming to improve cardiotoxicity prevention and management in oncology patients.
We conducted a retrospective analysis of cancer patients treated with anthracyclines, HER2-targeted therapies, and radiotherapy. Cardiac function was monitored via echocardiography, focusing on global longitudinal strain and left ventricular ejection fraction (LVEF). Cardiac troponins and natriuretic peptides were measured to detect subclinical cardiotoxicity, with patients stratified by TNM cancer stage and histopathology.
Our analysis identified a significant association between certain cytostatic treatments, such as anthracyclines and HER2-targeted therapies, and a reduction in LVEF, particularly in patients with advanced-stage cancer. Biomarker assessments indicated early signs of cardiotoxicity in patients before clinical symptoms emerged. The findings also demonstrated a higher prevalence of cardiovascular complications in patients with pre-existing risk factors.
This study highlights the importance of personalized treatment protocols in minimizing cardiotoxicity and improving the quality of life for oncology patients. Regular cardiac monitoring, combined with the use of biomarkers, can help identify high-risk patients early, allowing for timely interventions. Future research should focus on optimizing cardioprotective strategies to mitigate the cardiovascular risks associated with modern cancer therapies.
N/A (retrospective study).
背景/目的:心脏肿瘤学在应对癌症治疗引起的心血管并发症方面已变得至关重要。虽然治疗方法的进步提高了生存率,但也增加了心血管风险。本研究评估细胞毒性治疗的心脏毒性作用,研究肿瘤特征(如组织病理学和TNM分类)与心血管并发症之间的关系,旨在改善肿瘤患者心脏毒性的预防和管理。
我们对接受蒽环类药物、HER2靶向治疗和放疗的癌症患者进行了回顾性分析。通过超声心动图监测心脏功能,重点关注整体纵向应变和左心室射血分数(LVEF)。测量心肌肌钙蛋白和利钠肽以检测亚临床心脏毒性,并根据TNM癌症分期和组织病理学对患者进行分层。
我们的分析确定了某些细胞毒性治疗(如蒽环类药物和HER2靶向治疗)与LVEF降低之间存在显著关联,尤其是在晚期癌症患者中。生物标志物评估表明,患者在出现临床症状之前就有心脏毒性的早期迹象。研究结果还表明,有既往危险因素的患者心血管并发症的患病率更高。
本研究强调了个性化治疗方案在将心脏毒性降至最低并改善肿瘤患者生活质量方面的重要性。定期心脏监测结合生物标志物的使用有助于早期识别高危患者,从而及时进行干预。未来的研究应专注于优化心脏保护策略,以减轻与现代癌症治疗相关的心血管风险。
无(回顾性研究)。