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欧洲心脏病学会心脏肿瘤学指南生物标志物标准对癌症治疗相关心脏功能障碍发生率的影响

Impact of the ESC Cardio-Oncology Guidelines Biomarker Criteria on Incidence of Cancer Therapy-Related Cardiac Dysfunction.

作者信息

Mecinaj Albulena, Gulati Geeta, Ree Anne Hansen, Gravdehaug Berit, Røsjø Helge, Steine Kjetil, Wisløff Torbjørn, Geisler Jürgen, Omland Torbjørn, Heck Siri Lagethon

机构信息

K.G. Jebsen Center for Cardiac Biomarkers, Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.

Department of Cardiology, Division of Medicine, Akershus University Hospital, Lørenskog, Norway.

出版信息

JACC CardioOncol. 2024 Jan 16;6(1):83-95. doi: 10.1016/j.jaccao.2023.10.008. eCollection 2024 Feb.

Abstract

BACKGROUND

The impact of recent consensus definitions of cancer therapy-related cardiac dysfunction (CTRCD) from the European Society of Cardiology cardio-oncology guidelines on the reported incidence of CTRCD has not yet been assessed.

OBJECTIVES

The aim of this study was to assess the: 1) cumulative incidence; 2) point prevalence during and after adjuvant therapy; and 3) prognostic value of CTRCD as defined by different asymptomatic CTRCD guideline criteria.

METHODS

The cumulative incidence and point prevalence of CTRCD were retrospectively assessed in 118 patients participating in the PRADA (Prevention of Cardiac Dysfunction During Adjuvant Breast Cancer Therapy) trial. Asymptomatic CTRCD was assessed using alternative cardiac troponin (cTn) 99th percentile upper reference limits (URLs) to define cTnT and cTnI elevation.

RESULTS

The cumulative incidence of moderate or severe CTRCD was low (1.7%), whereas the cumulative incidence of mild asymptomatic CTRCD was higher and differed markedly according to the biomarker criteria applied, ranging from 49.2% of patients when cTnT greater than the sex-specific 99th percentile URL was used to define cTn elevation to 9.3% when sex-neutral cTnI was used. The point prevalence of CTRCD was highest at the end of anthracycline therapy (47.8%) and was driven primarily by asymptomatic cTn elevation. CTRCD during adjuvant therapy was not prognostic for CTRCD at extended follow-up of 24 months (Q1-Q3: 21-29 months) after randomization.

CONCLUSIONS

Mild asymptomatic CTRCD during adjuvant breast cancer therapy was frequent and driven mainly by cTn elevation and was not prognostic of subsequent CTRCD. The incidence of mild, asymptomatic CTRCD differed markedly depending on the cTn assay and whether sex-neutral or sex-dependent URLs were applied. (Prevention of Cardiac Dysfunction During Adjuvant Breast Cancer Therapy [PRADA]; NCT01434134).

摘要

背景

欧洲心脏病学会心脏肿瘤学指南中关于癌症治疗相关心脏功能障碍(CTRCD)的最新共识定义对所报告的CTRCD发病率的影响尚未得到评估。

目的

本研究的目的是评估:1)累积发病率;2)辅助治疗期间及之后的时点患病率;3)不同无症状CTRCD指南标准所定义的CTRCD的预后价值。

方法

对参与PRADA(辅助性乳腺癌治疗期间心脏功能障碍的预防)试验的118例患者进行回顾性评估,以确定CTRCD的累积发病率和时点患病率。使用替代心肌肌钙蛋白(cTn)第99百分位数上限参考值(URL)评估无症状CTRCD,以定义cTnT和cTnI升高。

结果

中度或重度CTRCD的累积发病率较低(1.7%),而轻度无症状CTRCD的累积发病率较高,且根据所应用的生物标志物标准有显著差异,范围从使用cTnT大于性别特异性第99百分位数URL来定义cTn升高时的49.2%的患者到使用性别中性cTnI时的9.3%。CTRCD的时点患病率在蒽环类药物治疗结束时最高(47.8%),主要由无症状cTn升高所致。在随机分组后24个月(第1四分位数 - 第3四分位数:21 - 29个月)的延长随访中,辅助治疗期间的CTRCD对CTRCD并无预后价值。

结论

辅助性乳腺癌治疗期间轻度无症状CTRCD很常见,主要由cTn升高所致,且对后续CTRCD并无预后价值。轻度无症状CTRCD的发病率根据cTn检测方法以及是否应用性别中性或性别特异性URL有显著差异。(辅助性乳腺癌治疗期间心脏功能障碍的预防[PRADA];NCT01434134)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45b6/10950440/cd4d462c4a48/ga1.jpg

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