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心脏毒性的可预测性:比利时心脏肿瘤学临床经验。

Predictability of cardiotoxicity: Experience of a Belgian cardio-oncology clinic.

机构信息

Department of Cardiovascular Sciences, KU Leuven, Campus Gasthuisberg O&N1, Herestraat 49, box 911, 3000 Leuven, Belgium.

Leuven Biostatistics and Statistical Bioinformatics Centre (L-Biostat), U.Z. Sint-RafaëlKapucijnenvoer 35, blok D, bus 7001B-3000 Leuven, Belgium.

出版信息

Int J Cardiol. 2022 Sep 15;363:119-122. doi: 10.1016/j.ijcard.2022.06.063. Epub 2022 Jun 28.

Abstract

BACKGROUND

New oncological treatments improved survival but also increased awareness of cardiovascular side-effects during and after cancer therapy.

METHODS

We report the experience of the cardio-oncology clinic at a large Belgian tertiary care center and investigated the predictability of cardiotoxicity based on referring department, cardiovascular risk factors, cancer treatment and existing risk scores of the American Society of Clinical Oncologists (ASCO) and Mayo Clinic. Cardiotoxicity was defined as a 10% reduction in Left Ventricular Ejection Fraction (LVEF) compared to the baseline transthoracic echocardiography (TTE) in asymptomatic patients or 5% in symptomatic patients.

RESULTS

Of the 324 patients included, 14.5% died during follow-up. Most deaths were oncological, yet 19% of deaths were attributable to cardiovascular diseases. Models based on cardiovascular risk factors alone and cardiovascular risk factors combined with cardiotoxic medication poorly predicted cardiotoxicity. Existing risk scores from ASCO and Mayo Clinic also poorly predicted cardiotoxicity. A weighed model based on the Mayo Clinic cardiotoxicity risk score was the best risk assessment tool with still a limited predictive value with an Area Under the Receiver Operating Characteristic curve of 0.654 (CI 95%: 0.601-0.715).

CONCLUSION

Cardiovascular morbidity and mortality are common in cancer patients and survivors and stress the unmet need of adequate risk prediction tools for systematic screening and rigorous cardiovascular follow-up. In our outpatient cohort, cardiotoxicity risk could not be adequately predicted by cancer type, using classic cardiovascular risk factors, nor by the combination of cardiovascular risk factors and the proposed cancer treatment. Furthermore, we showed that existing cardiotoxicity risk scores are suboptimal and should thus be interpreted with caution.

摘要

背景

新的肿瘤治疗方法提高了生存率,但也增加了对癌症治疗期间和治疗后心血管副作用的认识。

方法

我们报告了一家大型比利时三级护理中心的心脏肿瘤学诊所的经验,并根据转诊科室、心血管危险因素、癌症治疗以及美国临床肿瘤学会(ASCO)和梅奥诊所的现有风险评分,调查了心脏毒性的可预测性。心脏毒性定义为无症状患者左心室射血分数(LVEF)与基线经胸超声心动图(TTE)相比下降 10%,或有症状患者下降 5%。

结果

在 324 名纳入的患者中,14.5%在随访期间死亡。大多数死亡是癌症相关的,但 19%的死亡归因于心血管疾病。仅基于心血管危险因素和心血管危险因素联合心脏毒性药物的模型对心脏毒性的预测效果不佳。ASCO 和梅奥诊所的现有风险评分也不能很好地预测心脏毒性。基于梅奥诊所心脏毒性风险评分的加权模型是最佳风险评估工具,但预测价值有限,受试者工作特征曲线下面积为 0.654(95%CI:0.601-0.715)。

结论

心血管发病率和死亡率在癌症患者和幸存者中很常见,强调需要有足够的风险预测工具来进行系统筛查和严格的心血管随访。在我们的门诊队列中,不能通过癌症类型、使用经典心血管危险因素或心血管危险因素与拟议的癌症治疗相结合来充分预测心脏毒性风险。此外,我们表明现有的心脏毒性风险评分并不理想,因此应谨慎解释。

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