Feasibility Study for Long-Term Cardiotoxicity in Dose-Dense Treated Cancer Patients.

International journal of heart failure Pub Date : 2025-04-21 eCollection Date: 2025-04-01 DOI:10.36628/ijhf.2024.0056
Markus B Heckmann, Julia Lehmann, Daniel Finke, Florian Roll, Norbert Frey, Andreas Schneeweiss, Frederik Marmé, Lorenz H Lehmann
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Abstract

Background and objectives: Dose-dense anthracycline-based chemotherapy has emerged as a critical strategy in managing high-risk breast cancer, offering survival benefits through increased dose intensity or shortened intervals. While short-term studies report preserved left ventricular ejection fraction (LVEF), the long-term cardiotoxicity of such regimens, especially at accelerated intervals, remains inadequately explored. Aim of this study was to evaluate the long-term cardiac safety of dose-dense anthracycline-based chemotherapy compared to conventional protocols in patients with non-metastatic breast cancer.

Methods: This retrospective study included 101 breast cancer patients treated at the National Center for Tumor Diseases, Heidelberg, between 2007 and 2014. Patients were classified into dose-dense (n=44) or conventional therapy (n=57) groups. Long-term follow-up (7-10 years post-treatment) comprised echocardiography with global longitudinal strain (GLS), electrocardiography, and cardiac biomarkers. Statistical analyses were conducted using Cox regression, and competing risks models.

Results: Left ventricular systolic function was preserved in both groups, with no significant differences in LVEF (58.1±5.4% in the dose-dense group and 59.6±3.7% in the conventional therapy group, p=0.341) or GLS. Diastolic dysfunction affected 28.6% of the dose-dense group and 47.4% of the conventional group, with age (odds ratio [OR], 1.14 per year; p=0.038) and hypertension (OR, 10.50; p=0.011) emerging as key predictors. Only one case of anthracycline-induced heart failure was reported. Mortality was primarily tumor-related, highlighting limited cardiac contributions to overall survival.

Conclusions: Dose-dense anthracycline therapy demonstrated comparable long-term cardiac safety to conventional regimens, with preserved systolic function and minimal heart failure incidence. These findings underscore the importance of individualized risk assessment and comprehensive cardiac monitoring in breast cancer management.

剂量密集治疗的癌症患者长期心脏毒性的可行性研究。
背景和目的:以剂量密集蒽环类药物为基础的化疗已成为治疗高危乳腺癌的关键策略,通过增加剂量强度或缩短间隔提供生存益处。虽然短期研究报告保留了左心室射血分数(LVEF),但这些方案的长期心脏毒性,特别是在加速间隔时,仍未充分探讨。本研究的目的是评估在非转移性乳腺癌患者中,与传统方案相比,剂量密集蒽环类化疗的长期心脏安全性。方法:本回顾性研究纳入2007年至2014年在海德堡国家肿瘤疾病中心接受治疗的101例乳腺癌患者。将患者分为剂量密集组(n=44)和常规治疗组(n=57)。长期随访(治疗后7-10年)包括超声心动图和全局纵向应变(GLS)、心电图和心脏生物标志物。采用Cox回归和竞争风险模型进行统计分析。结果:两组患者左室收缩功能均保持正常,LVEF(剂量密集组为58.1±5.4%,常规治疗组为59.6±3.7%,p=0.341)和GLS差异无统计学意义。舒张功能障碍影响剂量密集组的28.6%和常规组的47.4%,与年龄有关(优势比[OR], 1.14 /年;p=0.038)和高血压(OR, 10.50;P =0.011)成为关键预测因子。仅报道一例蒽环类药物引起的心力衰竭。死亡率主要与肿瘤相关,强调心脏对总生存率的贡献有限。结论:剂量密集的蒽环类药物治疗与传统方案相比具有相当的长期心脏安全性,具有保留收缩功能和最小心力衰竭发生率。这些发现强调了个体化风险评估和全面心脏监测在乳腺癌管理中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
6.30
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