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儿童癌症治疗患者的心血管毒性:美国心脏协会的科学声明

Cardiovascular Toxicity in Patients Treated for Childhood Cancer: A Scientific Statement From the American Heart Association.

作者信息

Ryan Thomas D, Bates James E, Kinahan Karen E, Leger Kasey J, Mulrooney Daniel A, Narayan Hari K, Ness Kirsten, Okwuosa Tochukwu M, Rainusso Nino C, Steinberger Julia, Armenian Saro H

出版信息

Circulation. 2025 Apr 15;151(15):e926-e943. doi: 10.1161/CIR.0000000000001308. Epub 2025 Mar 19.


DOI:10.1161/CIR.0000000000001308
PMID:40104841
Abstract

The field of cardio-oncology has expanded over the past 2 decades to address the ever-increasing issues related to cardiovascular disease in patients with cancer and survivors. There is increasing recognition that nearly all cancer treatments pose some short- or long-term risk for development of cardiovascular disease and that pediatric patients with cancer may be especially vulnerable to cardiovascular disease because of young age at treatment and expected long life span afterward. Anthracycline chemotherapy and chest-directed radiotherapy are the most well-studied cardiotoxic therapies, and dose reduction, use of cardioprotection for anthracyclines, and modern radiotherapy approaches have contributed to improved cardiovascular outcomes for survivors. Newer treatments such as small-molecule inhibitors, antibody-based cytotoxic therapy, and immunotherapy have expanded options for previously difficult-to-treat cancers but have also revealed new cardiotoxic profiles. Application of effective surveillance strategies in patients with cancer and survivors has been a focus of practitioners and researchers, whereas the prevention and treatment of extant cardiovascular disease is still developing. Incorporation of new strategies in an equitable manner and appropriate transition from pediatric to adult care will greatly influence long-term health-related outcomes in the growing population of childhood cancer survivors at risk for cardiovascular disease.

摘要

在过去20年中,心脏肿瘤学领域不断扩展,以应对癌症患者及其幸存者中与心血管疾病相关的日益增多的问题。人们越来越认识到,几乎所有癌症治疗都对心血管疾病的发生构成一些短期或长期风险,而且癌症患儿可能因其治疗时年龄小以及后续预期寿命长而特别容易患心血管疾病。蒽环类化疗和胸部定向放疗是研究最充分的心脏毒性治疗方法,剂量减少、对蒽环类药物使用心脏保护措施以及现代放疗方法都有助于改善幸存者的心血管结局。小分子抑制剂、基于抗体的细胞毒性疗法和免疫疗法等新型治疗方法为以前难以治疗的癌症提供了更多选择,但也揭示了新的心脏毒性特征。在癌症患者及其幸存者中应用有效的监测策略一直是从业者和研究人员关注的焦点,而现存心血管疾病的预防和治疗仍在发展中。以公平的方式纳入新策略以及从儿科到成人护理的适当过渡,将极大地影响越来越多有心血管疾病风险的儿童癌症幸存者的长期健康相关结局。

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Cardiovascular Toxicity in Patients Treated for Childhood Cancer: A Scientific Statement From the American Heart Association.

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引用本文的文献

[1]
The Role of miRNAs as Predictors of Acute Lymphoblastic Leukemia Chemotherapy Toxicity in Children: A Systematic Review.

J Clin Med. 2025-8-20

[2]
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[3]
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[4]
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本文引用的文献

[1]
The Children's Oncology Group Long-Term Follow-Up Guidelines for Survivors of Childhood, Adolescent, and Young Adult Cancers: A Review.

JAMA Oncol. 2025-5-1

[2]
Cardiac Dysfunction in Children and Young Adults Treated With MEK Inhibitors: A Retrospective, Single-Center Study.

JACC CardioOncol. 2024-8-6

[3]
Strain surveillance during chemotherapy to improve cardiovascular outcomes: the SUCCOUR-MRI trial.

Eur Heart J. 2024-11-7

[4]
Cardiotoxic profiles of CAR-T therapy and bispecific T-cell engagers in hematological cancers.

Commun Med (Lond). 2024-6-13

[5]
A Biomarker-Based Diagnostic Model for Cardiac Dysfunction in Childhood Cancer Survivors.

JACC CardioOncol. 2024-4-16

[6]
A comprehensive pediatric cardio-oncology program: a single institution approach to cardiovascular care for pediatric patients with cancer and childhood cancer survivors.

Cardiooncology. 2024-4-6

[7]
Acute Promyelocytic Leukemia: Review of Complications Related to All-Trans Retinoic Acid and Arsenic Trioxide Therapy.

Cancers (Basel). 2024-3-15

[8]
Presence and utility of electrocardiographic abnormalities in long-term childhood cancer survivors.

Heart. 2024-4-25

[9]
Mortality After Major Cardiovascular Events in Survivors of Childhood Cancer.

J Am Coll Cardiol. 2024-2-27

[10]
Effect of carvedilol versus placebo on cardiac function in anthracycline-exposed survivors of childhood cancer (PREVENT-HF): a randomised, controlled, phase 2b trial.

Lancet Oncol. 2024-2

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