Soluble urokinase plasminogen activator receptor and cardiotoxicity in doxorubicin-treated breast cancer patients: a prospective exploratory study.

IF 3.2 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Jian Chu, Lillian Tung, Issam Atallah, Changli Wei, Melody Cobleigh, Ruta Rao, Steven B Feinstein, Lydia Usha, Kathrin Banach, Jochen Reiser, Tochukwu M Okwuosa
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引用次数: 0

Abstract

Background: Soluble urokinase plasminogen activator receptor is an inflammatory biomarker that may prognosticate cardiovascular outcomes. We sought to determine the associations between soluble urokinase plasminogen activator receptor and established markers of cardiotoxicity in breast cancer patients receiving doxorubicin.

Methods: We conducted a prospective cohort study of women with newly diagnosed breast cancer receiving standard-dose doxorubicin (240 mg/m2) at Rush University Medical Center and Rush Oak Park Hospital (Chicago, IL) between January 2017 and May 2019. Left ventricular ejection fraction, global longitudinal strain, and cardiac biomarkers (N-terminal prohormone B-type natriuretic peptide, troponin-I, and high-sensitivity C-reactive protein) were measured at baseline and at intervals up to 12-month follow-up after end of treatment. The associations between soluble urokinase plasminogen activator receptor and these endpoints were evaluated using multivariable mixed effects linear regression.

Results: Our study included 37 women (mean age 47.0 ± 9.3 years, 60% white) with a median baseline soluble urokinase plasminogen activator receptor level of 2.83 ng/dL. No participant developed cardiomyopathy based on serial echocardiography by one-year follow-up. The median percent change in left ventricular strain was -4.3% at 6-month follow-up and absolute changes in cardiac biomarkers were clinically insignificant. There were no significant associations between soluble urokinase plasminogen activator receptor and these markers of cardiotoxicity (all p > 0.05).

Conclusions: In this breast cancer cohort, doxorubicin treatment was associated with a very low risk for cardiotoxicity. Across this narrow range of clinical endpoints, soluble urokinase plasminogen activator receptor was not associated with markers of subclinical cardiotoxicity. Further studies are needed to clarify the prognostic utility of soluble urokinase plasminogen activator receptor in doxorubicin-associated cardiomyopathy and should include a larger cohort of leukemia and lymphoma patients who receive higher doses of doxorubicin.

可溶性尿激酶纤溶酶原激活物受体与多柔比星治疗的乳腺癌患者的心脏毒性:一项前瞻性探索研究。
背景:可溶性尿激酶纤溶酶原激活物受体是一种炎性生物标志物,可预示心血管疾病的预后。我们试图确定接受多柔比星治疗的乳腺癌患者体内可溶性尿激酶纤溶酶原激活物受体与已确定的心脏毒性标志物之间的关联:我们对2017年1月至2019年5月期间在拉什大学医学中心和拉什橡树园医院(伊利诺伊州芝加哥)接受标准剂量多柔比星(240 mg/m2)治疗的新诊断乳腺癌女性患者进行了一项前瞻性队列研究。研究人员在基线和治疗结束后12个月的随访期间测量了左心室射血分数、整体纵向应变和心脏生物标志物(N-末端原B型钠尿肽、肌钙蛋白-I和高敏C反应蛋白)。使用多变量混合效应线性回归评估了可溶性尿激酶纤溶酶原激活物受体与这些终点之间的关系:我们的研究包括 37 名女性(平均年龄 47.0 ± 9.3 岁,60% 为白人),可溶性尿激酶纤溶酶原激活物受体的基线中位水平为 2.83 ng/dL。根据连续超声心动图检查结果,一年随访期间没有人出现心肌病变。随访6个月时,左心室应变的中位变化率为-4.3%,心脏生物标志物的绝对变化在临床上并不显著。可溶性尿激酶纤溶酶原激活物受体与这些心脏毒性标志物之间没有明显的关联(P均大于0.05):结论:在这一乳腺癌队列中,多柔比星治疗引起心脏毒性的风险非常低。在这一范围较窄的临床终点中,可溶性尿激酶纤溶酶原激活物受体与亚临床心脏毒性标志物无关。要明确可溶性尿激酶纤溶酶原激活物受体在多柔比星相关心肌病中的预后作用,还需要进一步的研究,并应包括接受高剂量多柔比星治疗的更大规模的白血病和淋巴瘤患者。
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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来源期刊
Cardio-oncology
Cardio-oncology Medicine-Cardiology and Cardiovascular Medicine
CiteScore
5.00
自引率
3.00%
发文量
17
审稿时长
7 weeks
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