Monti Caterina Beatrice, Zanardo Moreno, Bosetti Tommaso, Alì Marco, De Benedictis Elena, Luporini Alberto, Secchi Francesco, Sardanelli Francesco
Department of Biomedical Sciences for Health, Università degli Studi di Milano, Via Mangiagalli 31, 20133 Milan, Italy.
Medicine and Surgery School, Università degli Studi di Milano, Via Festa del Perdono 7, 20122 Milan, Italy.
Quant Imaging Med Surg. 2020 May;10(5):934-944. doi: 10.21037/qims.2020.04.05.
Cancer treatment with anthracyclines may lead to an increased incidence of cardiac disease due to cardiotoxicity, as they may cause irreversible myocardial fibrosis. So far, the proposed methods for screening patients for cardiotoxicity have led to only limited success, while the analysis of myocardial extracellular volume (mECV) at cardiac magnetic resonance (CMR) has shown promising results, albeit requiring a dedicated exam. Recent studies have found strong correlations between mECV values obtained through computed tomography (CT), and those derived from CMR. Thus, our purpose was to evaluate the feasibility of estimating mECV on thoracic contrast-enhanced CT performed for staging or follow-up in breast cancer patients treated with anthracyclines, and, if feasible, to assess if a rise in mECV is associated with chemotherapy, and persistent over time.
After ethics committee approval, female patients with breast cancer who had undergone at least 2 staging or follow-up CT examinations at our institution, one before and one shortly after the end of chemotherapy including anthracyclines were retrospectively evaluated. Patients without available haematocrit, with artefacts in CT images, or who had undergone radiation therapy of the left breast were excluded. Follow-up CT examinations at longer time intervals were also analysed, when available. mECV was calculated on scans obtained at 1, and 7 min after contrast injection.
Thirty-two female patients (aged 57±13 years) with pre-treatment haematocrit 38%±4%, and ejection fraction 64%±6% were analysed. Pre-treatment mECV was 27.0%±2.9% at 1 min, and 26.4%±3.8% at 7 min, similar to values reported for normal subjects in the literature. Post-treatment mECV (median interval: 89 days after treatment) was 31.1%±4.9%, and 30.0%±5.1%, respectively, values significantly higher than pre-treatment values at all times (P<0.005). mECV at follow-up (median interval: 135 days after post-treatment CT) was 31.0%±4.5%, and 27.7%±3.7%, respectively, without significant differences (P>0.548) when compared to post-treatment values.
mECV values from contrast-enhanced CT scans could play a role in the assessment of myocardial condition in breast cancer patients undergoing anthracycline-based chemotherapy. CT-derived ECV could be an imaging biomarker for the monitoring of therapy-related cardiotoxicity, allowing for potential secondary prevention of cardiac damage, using data derived from an examination that could be already part of patients' clinical workflow.
由于具有心脏毒性,使用蒽环类药物进行癌症治疗可能会导致心脏病发病率增加,因为它们可能会引起不可逆的心肌纤维化。到目前为止,所提出的用于筛查心脏毒性患者的方法仅取得了有限的成功,而心脏磁共振成像(CMR)对心肌细胞外容积(mECV)的分析已显示出有前景的结果,尽管这需要专门的检查。最近的研究发现,通过计算机断层扫描(CT)获得的mECV值与通过CMR获得的值之间存在很强的相关性。因此,我们的目的是评估在接受蒽环类药物治疗的乳腺癌患者进行分期或随访的胸部增强CT上估计mECV的可行性,如果可行,评估mECV的升高是否与化疗相关,并随时间持续存在。
经伦理委员会批准后,对在我们机构接受过至少2次分期或随访CT检查的乳腺癌女性患者进行回顾性评估,其中一次在化疗(包括蒽环类药物)结束前,一次在结束后不久。排除没有可用血细胞比容、CT图像有伪影或接受过左乳放射治疗的患者。如有可用的,还分析了较长时间间隔的随访CT检查。在注射造影剂后1分钟和7分钟获得的扫描图像上计算mECV。
分析了32名女性患者(年龄57±13岁),治疗前血细胞比容为38%±4%,射血分数为64%±6%。治疗前1分钟时mECV为27.0%±2.9%,7分钟时为26.4%±3.8%,与文献中报道的正常受试者的值相似。治疗后mECV(中位间隔:治疗后89天)分别为31.1%±4.9%和30.0%±5.1%,在所有时间点均显著高于治疗前值(P<0.005)。随访时(中位间隔:治疗后CT检查后135天)mECV分别为31.0%±4.5%和27.7%±3.7%,与治疗后值相比无显著差异(P>0.548)。
对比增强CT扫描获得的mECV值可在评估接受蒽环类药物化疗的乳腺癌患者的心肌状况中发挥作用。CT衍生的ECV可能是监测治疗相关心脏毒性的一种影像学生物标志物,利用来自一项可能已成为患者临床工作流程一部分的检查的数据,有可能对心脏损伤进行二级预防。