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

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 radioth...

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Bibliographic Details
Published inFrontiers in oncology Vol. 12; p. 706861
Main Authors Fu, Zhenkun, Lin, Zhoujun, Yang, Mao, Li, Chenggang
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 24.03.2022
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Summary: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.
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This article was submitted to Breast Cancer, a section of the journal Frontiers in Oncology
Reviewed by: Masahiko Tanabe, The University of Tokyo, Japan; Christiane Matuschek, University Hospital of Düsseldorf, Germany
Edited by: Noam Falbel Pondé, A.C.Camargo Cancer Center, Brazil
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2022.706861