Pharmaceutical compositions and methods for countering chemotherapy induced cardiotoxicity
This disclosure provides methods and pharmaceutical compositions for reducing or eliminating cardiotoxicity, particularly cardiotoxicity induced by a cancer treatment or other therapy. In some cases, the methods and compositions prevent or reduce cardiotoxicity caused by anthracycline treatment. The methods provided herein often comprise administering a protective agent such as myricetin, tricetin, robinetin, ficetin, vitexin, quercetin, dihydrorobinetin, kaempferol, 7,3′,4′,5′-tetrahydroxyflavone, and myricitrin in conjunction with the administration of a cancer drug or other treatment. They may comprise administering a protective agent in combination with dexrazoxane. The compositions provided herein include co-formulations of a protective agent with a different protective agent or with a cancer treatment (e.g., anthracycline drug).
1. A method for preventing, reducing, or eliminating cardiotoxicity induced by an anticancer agent in a subject, the method comprising administering to the subject an effective amount of a protective agent prior to or simultaneously with the anticancer agent, wherein the protective agent is myricetin or salt thereof, wherein the anticancer agent is a protein kinase inhibitor or a proteasome inhibitor, and wherein the administration of the protective agent provides an effective amount of myricetin or salt thereof in the subject, thereby preventing, reducing, or eliminating the cardiotoxicity induced by the anticancer agent.
2. The method of claim 1 , wherein the protective agent is administered to the subject at least about 5 minutes before the administration of the anticancer agent.
3. The method of claim 1 , wherein the protective agent and the anticancer agent are administered simultaneously.
4. The method of claim 3 , wherein the protective agent and the anticancer agent are co-formulated in a liquid composition.
5. The method of claim 1 , wherein the cardiotoxicity comprises one or more of cardiac tissue damage, electrophysiological dysfunction, contractile dysfunction, DNA double strand break in cardiomyocytes, mitochondrial toxicity, apoptosis, and oxidative stress.
6. A method for treating cancer in a subject, the method comprising:
(i) administering to the subject an effective amount of an anticancer agent; and
(ii) administering to the subject an effective amount of a protective agent prior to or simultaneously with the anticancer agent;
wherein the protective agent is myricetin or salt thereof;
wherein the anticancer agent is a protein kinase inhibitor or a proteasome inhibitor; and
wherein the administration of the protective agent prevents, reduces, or eliminates cardiotoxicity induced by the anticancer agent in the subject.
7. The method of claim 6 , wherein the protective agent is administered to the subject at least about 5 minutes before the administration of the anticancer agent.
8. The method of claim 6 , wherein the protective agent and the anticancer agent are administered simultaneously.
9. The method of claim 1 , wherein the protein kinase inhibitor is selected from the group consisting of afatinib, axitinib, bosutinib, cabozantinib, carfilzomib, ceritinib, cobimetanib, crizotinib, dabrafenib, dasatinib, erlotinib, everolimus, gefitinib, ibrutinib, imatinib, lapatinib, lenvatinib, nilotinib, nintedanib, osimertinib, palbociclib, pazopanib, pegaptanib, ponatinib, regorafenib, ruxolitinib, sirolimus, sorafenib, sunitinib, tofacitinib, tofacitinib, temsirolimus, trametinib, vandetanib, vemurafenib, and vismodegib.
10. The method of claim 1 , wherein the protein kinase inhibitor is a tyrosine kinase inhibitor.
11. The method of claim 10 , wherein the tyrosine kinase inhibitor is selected from the group consisting of sorafenib, sunitinib, bosutinib, gefitinib, dasatinib, dabrafenib, vemurafenib, imatinib, lapatinib, and nilotinib.
12. The method of claim 10 , wherein the tyrosine kinase inhibitor is sorafenib or sunitinib.