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乳腺癌术后辅助靶向治疗引起的心脏毒性

Cardiac Toxicity From Adjuvant Targeting Treatment for Breast Cancer Post-Surgery.

作者信息

Fu Zhenkun, Lin Zhoujun, Yang Mao, Li Chenggang

机构信息

Department of Immunology & Wu Lien-Teh Institute & Heilongjiang Provincial Key Laboratory for Infection and Immunity, Harbin Medical University & Heilongjiang Academy of Medical Science, Harbin, China.

State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, China.

出版信息

Front Oncol. 2022 Mar 24;12:706861. doi: 10.3389/fonc.2022.706861. eCollection 2022.

Abstract

Breast cancer is one of the most prevalent types of cancers worldwide, especially for females. Surgery is the preferred treatment for breast cancer, and various postoperative adjuvant therapies can be reasonably used according to different pathological characteristics, especially traditional radiotherapy, chemotherapy, and endocrine therapy. In recent years, targeting agent therapy has also become one of the selective breast cancer treatment strategies, including anti-HER-2 drugs, CDK4/6 inhibitor, poly ADP-ribose polymerase inhibitor, PI3K/AKT/mTOR pathway inhibitor, ER targeting drugs, and aromatase inhibitor. Because of the different pathologic mechanisms of these adjuvant therapies, each of the strategies may cause cardiotoxicity in clinic. The cardiac adverse events of traditional endocrine therapy, radiotherapy, and chemotherapy for breast cancer have been widely detected in clinic; however, the targeting therapy agents have been paid more attention with the extension of application. This review will summarize the cardiac toxicity of various adjuvant therapies for breast cancer, especially for targeting drug therapy.

摘要

乳腺癌是全球最常见的癌症类型之一,尤其是在女性群体中。手术是乳腺癌的首选治疗方法,根据不同的病理特征可合理使用各种术后辅助治疗,特别是传统的放疗、化疗和内分泌治疗。近年来,靶向药物治疗也已成为乳腺癌选择性治疗策略之一,包括抗HER-2药物、CDK4/6抑制剂、聚ADP-核糖聚合酶抑制剂、PI3K/AKT/mTOR通路抑制剂、雌激素受体靶向药物和芳香化酶抑制剂。由于这些辅助治疗的病理机制不同,每种策略在临床上都可能导致心脏毒性。乳腺癌传统内分泌治疗、放疗和化疗的心脏不良事件在临床上已被广泛检测到;然而,随着靶向治疗药物应用的推广,其受到了更多关注。本综述将总结乳腺癌各种辅助治疗的心脏毒性,尤其是靶向药物治疗的心脏毒性。

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