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Delivery of epirubicin via slow infusion as a strategy to mitigate chemotherapy-induced cardiotoxicity

BACKGROUND: Continuous infusion of doxorubicin has been a strategy to reduce cardiotoxicity. Epirubicin is another anthracycline in common clinical use. However, evidence is lacking regarding whether this strategy can reduce cardiotoxicity of epirubicin without compromising antineoplastic efficacy....

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Autores principales: Yang, Fang, Lei, Qiao, Li, Lu, He, Jian Chang, Zeng, Jiajia, Luo, Chunxiang, Yeung, Sai-Ching Jim, Yang, Runxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683617/
https://www.ncbi.nlm.nih.gov/pubmed/29131861
http://dx.doi.org/10.1371/journal.pone.0188025
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author Yang, Fang
Lei, Qiao
Li, Lu
He, Jian Chang
Zeng, Jiajia
Luo, Chunxiang
Yeung, Sai-Ching Jim
Yang, Runxiang
author_facet Yang, Fang
Lei, Qiao
Li, Lu
He, Jian Chang
Zeng, Jiajia
Luo, Chunxiang
Yeung, Sai-Ching Jim
Yang, Runxiang
author_sort Yang, Fang
collection PubMed
description BACKGROUND: Continuous infusion of doxorubicin has been a strategy to reduce cardiotoxicity. Epirubicin is another anthracycline in common clinical use. However, evidence is lacking regarding whether this strategy can reduce cardiotoxicity of epirubicin without compromising antineoplastic efficacy. DESIGN AND METHODS: Healthy rats were randomized into groups: epirubicin (8 mg/kg) delivered intraperitoneally via micro osmotic pumps (MOP), epirubicin (8 mg/kg) by intraperitoneal (IP) bolus injection, and placebo control. Blood samples were collected for analyzing biomarkers of myocardial injury and pharmacokinetics. At chosen times, sub-groups of animals were sacrificed for histopathology. A mouse breast cancer cell line (4T1), stably transfected with luciferase, was orthotopically allografted in female mice, and treated in three groups as described above for the rats. Tumor growth was monitored by measuring tumor size as well as bioluminescence. RESULTS: Delivery by IP bolus and by MOP achieved essentially the same area under the curve of epirubicin plasma concentration time profile. Blood biomarkers showed that the degree of myocardial injury in MOP group was lower than that of IP group. Histopathology showed that there was less eosinophilic enhancement, interstitial hemorrhage and necrotizing muscle atrophy in MOP group than IP group. In the orthotopic breast cancer allograft mouse model, the antineoplastic effect of epirubicin by MOP was not different from that by IP as measured by tumor weights or by in vivo bioluminescence. CONCLUSION: Slow delivery of epirubicin by MOP reduced cardiotoxicity without compromising the antineoplastic effect compared to IP bolus delivery. These in vivo data support our previous clinical data that continuous intravenous infusion of epirubicin using micro infusion pumps over 48–96 hours had less cardiotoxicity than intravenous bolus injections. However, whether multiple doses of epirubicin given by MOP result in a lower magnitude of long term cardiomyopathy remains to be further investigated.
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spelling pubmed-56836172017-11-30 Delivery of epirubicin via slow infusion as a strategy to mitigate chemotherapy-induced cardiotoxicity Yang, Fang Lei, Qiao Li, Lu He, Jian Chang Zeng, Jiajia Luo, Chunxiang Yeung, Sai-Ching Jim Yang, Runxiang PLoS One Research Article BACKGROUND: Continuous infusion of doxorubicin has been a strategy to reduce cardiotoxicity. Epirubicin is another anthracycline in common clinical use. However, evidence is lacking regarding whether this strategy can reduce cardiotoxicity of epirubicin without compromising antineoplastic efficacy. DESIGN AND METHODS: Healthy rats were randomized into groups: epirubicin (8 mg/kg) delivered intraperitoneally via micro osmotic pumps (MOP), epirubicin (8 mg/kg) by intraperitoneal (IP) bolus injection, and placebo control. Blood samples were collected for analyzing biomarkers of myocardial injury and pharmacokinetics. At chosen times, sub-groups of animals were sacrificed for histopathology. A mouse breast cancer cell line (4T1), stably transfected with luciferase, was orthotopically allografted in female mice, and treated in three groups as described above for the rats. Tumor growth was monitored by measuring tumor size as well as bioluminescence. RESULTS: Delivery by IP bolus and by MOP achieved essentially the same area under the curve of epirubicin plasma concentration time profile. Blood biomarkers showed that the degree of myocardial injury in MOP group was lower than that of IP group. Histopathology showed that there was less eosinophilic enhancement, interstitial hemorrhage and necrotizing muscle atrophy in MOP group than IP group. In the orthotopic breast cancer allograft mouse model, the antineoplastic effect of epirubicin by MOP was not different from that by IP as measured by tumor weights or by in vivo bioluminescence. CONCLUSION: Slow delivery of epirubicin by MOP reduced cardiotoxicity without compromising the antineoplastic effect compared to IP bolus delivery. These in vivo data support our previous clinical data that continuous intravenous infusion of epirubicin using micro infusion pumps over 48–96 hours had less cardiotoxicity than intravenous bolus injections. However, whether multiple doses of epirubicin given by MOP result in a lower magnitude of long term cardiomyopathy remains to be further investigated. Public Library of Science 2017-11-13 /pmc/articles/PMC5683617/ /pubmed/29131861 http://dx.doi.org/10.1371/journal.pone.0188025 Text en © 2017 Yang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Yang, Fang
Lei, Qiao
Li, Lu
He, Jian Chang
Zeng, Jiajia
Luo, Chunxiang
Yeung, Sai-Ching Jim
Yang, Runxiang
Delivery of epirubicin via slow infusion as a strategy to mitigate chemotherapy-induced cardiotoxicity
title Delivery of epirubicin via slow infusion as a strategy to mitigate chemotherapy-induced cardiotoxicity
title_full Delivery of epirubicin via slow infusion as a strategy to mitigate chemotherapy-induced cardiotoxicity
title_fullStr Delivery of epirubicin via slow infusion as a strategy to mitigate chemotherapy-induced cardiotoxicity
title_full_unstemmed Delivery of epirubicin via slow infusion as a strategy to mitigate chemotherapy-induced cardiotoxicity
title_short Delivery of epirubicin via slow infusion as a strategy to mitigate chemotherapy-induced cardiotoxicity
title_sort delivery of epirubicin via slow infusion as a strategy to mitigate chemotherapy-induced cardiotoxicity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683617/
https://www.ncbi.nlm.nih.gov/pubmed/29131861
http://dx.doi.org/10.1371/journal.pone.0188025
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