Cardiotoxicity in Breast Cancer Therapy: Risks, Mechanisms, and Prevention Strategies.

IF 4.4 Q1 Medicine
Annisa Eka Fitrianti, Nadea Olyvia Wardani, Astri Astuti, Kusnandar Anggadiredja, Lia Amalia, Risani Andalasia Putri, Zulfan Zazuli
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引用次数: 0

Abstract

Breast cancer is the most prevalent cancer in women. Anthracyclines are commonly used as the first line of treatment, often combined with other agents, including trastuzumab. Despite their efficacy, both drugs pose a risk of cardiotoxicity, which may impair patients' quality of life (QoL) and hinder treatment persistence. Anthracycline-induced cardiotoxicity is dose-dependent and generally irreversible, whereas trastuzumab is associated with potentially reversible cardiac dysfunction. This review discusses the risk factors and biological mechanisms underlying chemotherapy-induced cardiotoxicity in breast cancer and explores effective strategies for prevention and treatment. It has been demonstrated that several cardioprotective strategies, such as treatments with angiotensin-converting enzyme inhibitors (ACEis), angiotensin receptor blockers (ARBs), beta-blockers, and dexrazoxane, can help lessen cardiotoxic effects. A better understanding of cardioprotective strategies may help optimize cancer treatment without compromising cardiovascular function.

Abstract Image

乳腺癌治疗中的心脏毒性:风险、机制和预防策略。
乳腺癌是女性中最常见的癌症。蒽环类药物通常用作一线治疗,通常与曲妥珠单抗等其他药物联合使用。尽管它们的疗效,这两种药物都存在心脏毒性的风险,这可能会损害患者的生活质量(QoL)并阻碍治疗的持久性。蒽环类药物引起的心脏毒性是剂量依赖性的,通常是不可逆的,而曲妥珠单抗与潜在可逆的心功能障碍相关。本文综述了乳腺癌化疗引起的心脏毒性的危险因素和生物学机制,并探讨了有效的预防和治疗策略。研究表明,几种心脏保护策略,如血管紧张素转换酶抑制剂(ACEis)、血管紧张素受体阻滞剂(ARBs)、-受体阻滞剂和右唑嗪,可以帮助减轻心脏毒性作用。更好地了解心脏保护策略可能有助于在不损害心血管功能的情况下优化癌症治疗。
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
CiteScore
9.00
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0.00%
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审稿时长
6 weeks
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