Post-transplant cyclophosphamide-induced cardiotoxicity: A comprehensive review.

IF 0.7 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of Cardiovascular and Thoracic Research Pub Date : 2024-01-01 Epub Date: 2024-12-23 DOI:10.34172/jcvtr.33230
Azin Alizadehasl, Bita Shahrami, Reza Rahbarghazi, Azam Yalameh Aliabadi, Seyedeh Fatemeh Hosseini Jebelli, Yasamin Afsari Zonooz, Hoda Hakimian, Farzaneh Fathi, Sara Forati, Aysa Rezabakhsh
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Abstract

Cyclophosphamide-induced cardiotoxicity, associated with its toxic metabolite acrolein, is a significant concern and unresolved issue, especially when cyclophosphamide is administrated in high doses. However, cardiotoxicity following low-dose cyclophosphamide has been also documented, especially in post-hematopoietic stem cell transplantation (post-HSCT) settings. Despite the involvement of multiple signaling pathways in cyclophosphamide-induced cardiomyopathy, the exact underlying mechanisms remain to be fully elucidated. This review outlines the current challenges of cyclophosphamide therapy in HSCT recipients. In addition, the promising therapeutic approaches by targeting acrolein's anti-angiogenic effect were thoroughly discussed to better manage post-HSCT cyclophosphamide-induced cardiotoxicity.

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移植后环磷酰胺诱发的心脏毒性:全面回顾。
环磷酰胺引起的心脏毒性与其毒性代谢物丙烯醛相关,是一个重大关切和未解决的问题,特别是当环磷酰胺以高剂量施用时。然而,低剂量环磷酰胺引起的心脏毒性也有文献记载,特别是在造血干细胞移植后(hsct后)。尽管环磷酰胺诱导的心肌病涉及多种信号通路,但其确切的潜在机制仍未完全阐明。这篇综述概述了环磷酰胺治疗在造血干细胞移植受者中的当前挑战。此外,本文还深入讨论了利用丙烯醛抗血管生成作用来更好地治疗hsct后环磷酰胺引起的心脏毒性的治疗方法。
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来源期刊
Journal of Cardiovascular and Thoracic Research
Journal of Cardiovascular and Thoracic Research CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
2.00
自引率
0.00%
发文量
22
审稿时长
7 weeks
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