Long-term impact of anthracycline in early-stage breast cancer, bridging of MiRNAs profiler for early cardiotoxicity.

IF 3.2 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Nattaya Poovorawan, Thiti Susiriwatananont, Chinachote Teerapakpinyo, Pajaree Chariyavilaskul, Piyada Sitthideatphaiboon, Luxica Jarutasnangkul, Monravee Tumkosit, Pairoj Chattranukulchai, Nonthikorn Theerasuwipakorn, Chatchawit Aporntewan, Shanop Shuangshoti, Sopark Manasnayakorn, Chanida Vinayanuwattikun, Yongkasem Vorasettakarnkij, Virote Sriuranpong
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引用次数: 0

Abstract

Background: Anthracyclines are essential in early breast cancer chemotherapy but pose long-term cardiotoxicity risks.

Objectives: This study aims to investigate the long-term incidence of cancer therapy-related cardiac dysfunction (CTRCD), bridging with the miRNAs profiler representing acute cardiac injury.

Methods: We conducted a prospective cohort including stage I-III breast cancer patients who received anthracycline between 2007 and 2012. Echocardiography was performed before and 12 weeks after anthracycline administration. The miRNAs profiler was conducted by NanoString and RT-PCR. Long-term cardiac magnetic resonance imaging (CMR) was evaluated in 24.2% of asymptomatic participants.

Results: At a median follow-up of 11 [IQR 6-12] years, 194 patients who completed follow-up echocardiography after anthracycline were included in the analysis. The median age at diagnosis was 50 [26-72] years. An early LVEF decline of ≥ 10% was found in 32.9% of participants. The cumulative equivalent dose of doxorubicin was 223.2 ± 21.6 mg/m2. At the time of censoring, sixty-four participants (32.9%) died, 70% from breast cancer. Nine participants (4.6%) reported cardiovascular events compatible with the CTRCD definition. Forty-seven participants (24.2%) underwent long-term cardiac evaluation. The miRNAs profiler and RT-PCR at different time points, 3 weeks and 6 weeks, respectively, revealed significantly diverse expressions of miR-1-3p and miR-16-5p in participants with and without an early LVEF decline of ≥ 10%. Despite cardiac injury demonstrated by dynamic miR-1-3p and miR-16-5p, CMR parameters revealed no significant differences.

Conclusions: Our study demonstrates a very low incidence of long-term symptomatic CTRCD. The diverse expression patterns of miR-16-5p and miR-1-3p at different time points also provide valuable biological insights. Within-normal results of an exact and comprehensive CMR, in asymptomatic and any LVEF change participants, indicate the long-term safety of limited-dose anthracycline-containing use.

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Abstract Image

Abstract Image

蒽环类药物对早期乳腺癌的长期影响,早期心脏毒性的mirna谱桥接。
背景:蒽环类药物在早期乳腺癌化疗中是必需的,但存在长期心脏毒性风险。目的:本研究旨在研究癌症治疗相关性心功能障碍(CTRCD)的长期发病率,并将其与代表急性心脏损伤的mirna谱连接起来。方法:我们进行了一项前瞻性队列研究,包括2007年至2012年间接受蒽环类药物治疗的I-III期乳腺癌患者。在给药前和给药后12周进行超声心动图检查。利用纳米链和RT-PCR技术进行miRNAs分析。24.2%的无症状参与者进行了长期心脏磁共振成像(CMR)评估。结果:中位随访11年[IQR 6-12], 194例蒽环类药物后完成超声心动图随访的患者纳入分析。诊断时的中位年龄为50岁[26-72]。32.9%的参与者早期LVEF下降≥10%。阿霉素累积等效剂量为223.2±21.6 mg/m2。在审查时,64名参与者(32.9%)死亡,其中70%死于乳腺癌。9名参与者(4.6%)报告了符合CTRCD定义的心血管事件。47名参与者(24.2%)接受了长期心脏评估。mirna谱仪和RT-PCR在不同时间点(分别为3周和6周)显示miR-1-3p和miR-16-5p在早期LVEF下降≥10%的参与者中表达差异显著。尽管动态miR-1-3p和miR-16-5p显示心脏损伤,但CMR参数显示无显著差异。结论:我们的研究表明长期症状性CTRCD的发生率非常低。miR-16-5p和miR-1-3p在不同时间点的不同表达模式也提供了有价值的生物学见解。在无症状和任何LVEF变化的参与者中,精确和全面的CMR结果在正常范围内,表明有限剂量含蒽环类药物的长期安全性。
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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