Department of Radiation Oncology, University Hospital, LMU Munich, Marchioninistraße 15, 81377, Munich, Germany.
Institute of Radiation Medicine, Helmholtz Center Munich, Munich, Germany.
Radiat Oncol. 2020 May 24;15(1):117. doi: 10.1186/s13014-020-01520-8.
Patients with left-sided breast cancer have an increased risk of cardiovascular disease (CVD) after radiotherapy (RT). While the awareness of cardiac toxicity has increased enormously over the last decade, the role of individual baseline cardiac risks has not yet been systematically investigated. Aim of the present study was to evaluate the impact of baseline CVD risks on radiation-induced cardiac toxicity.
Two hundred ten patients with left-sided breast cancer treated in the prospective Save-Heart Study using a deep inspiration breath-hold (DIBH) technique were analysed regarding baseline risk factors for CVD. Three frequently used prediction tools (Procam, Framingham and Reynolds score) were applied to evaluate the individual CVD risk profiles. Moreover, 10-year CVD excess absolute risks (EAR) were estimated using the individual mean heart dose (MHD) of treatment plans in free breathing (FB) and DIBH.
The individual baseline CVD risk factors had a strong impact on the 10-year cumulative CVD risk. The mean baseline risks of the non-diabetic cohort (n = 200) ranged from 3.11 to 3.58%, depending on the risk estimation tool. A large number of the non-diabetic patients had a very low 10-year CVD baseline risk of ≤1%; nevertheless, 8-9% of patients reached ≥10% baseline 10-year CVD risk. In contrast, diabetic patients (n = 10) had significantly higher baseline CVD risks (range: 11.76-24.23%). The mean 10-year cumulative risk (Framingham score) following RT was 3.73% using the DIBH-technique (MHD:1.42Gy) and 3.94% in FB (MHD:2.33Gy), after adding a 10-year-EAR of + 0.34%(DIBH) and + 0.55%(FB) to the baseline risks, respectively. Smoking status was one of the most important and modifiable baseline risk factors. After DIBH-RT, the 182 non-smoking patients had a mean 10-year cumulative risk of 3.55% (3.20% baseline risk, 0.35% EAR) as compared to 6.07% (5.60% baseline risk, 0.47% EAR) for the 28 smokers.
In the present study, all CVD prediction tools showed comparable results and could easily be integrated into daily clinical practice. A systematic evaluation and screening helps to identify high-risk patients who may benefit from primary prevention. This could result in an even higher benefit than from heart-sparing irradiation techniques alone.
接受放疗(RT)后,左侧乳腺癌患者患心血管疾病(CVD)的风险增加。尽管在过去十年中,人们对心脏毒性的认识有了极大的提高,但个体基线心脏风险的作用尚未得到系统研究。本研究旨在评估基线 CVD 风险对辐射诱导的心脏毒性的影响。
前瞻性 Save-Heart 研究中 210 例接受左侧乳腺癌治疗的患者使用深吸气屏气(DIBH)技术进行分析,评估 CVD 的基线风险因素。应用三种常用的预测工具(Procam、Framingham 和 Reynolds 评分)评估个体 CVD 风险概况。此外,使用 FB 和 DIBH 治疗计划中的个体平均心脏剂量(MHD)估算 10 年 CVD 超额绝对风险(EAR)。
个体基线 CVD 风险因素对 10 年累积 CVD 风险有很强的影响。非糖尿病队列(n=200)的平均基线风险范围为 3.11%至 3.58%,具体取决于风险估计工具。大多数非糖尿病患者的 CVD 基线 10 年风险非常低,≤1%;然而,8-9%的患者达到了≥10%的 CVD 基线 10 年风险。相比之下,糖尿病患者(n=10)的基线 CVD 风险明显更高(范围:11.76-24.23%)。使用 DIBH 技术(MHD:1.42Gy)时,RT 后患者 10 年累积风险(Framingham 评分)为 3.73%,FB 时为 3.94%(MHD:2.33Gy),分别在基线风险的基础上增加了 10 年-EAR(DIBH:+0.34%)和+0.55%(FB)。吸烟状态是最重要和最可改变的基线风险因素之一。与 28 名吸烟者相比,DIBH-RT 后 182 名不吸烟者的 10 年累积风险为 3.55%(3.20%基线风险,0.35%EAR)。
在本研究中,所有 CVD 预测工具均显示出可比的结果,并且可以轻松整合到日常临床实践中。系统评估和筛选有助于识别高危患者,这些患者可能受益于一级预防。这可能比单纯使用心脏保护照射技术带来更高的获益。