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Article: Treatment with trimetazidine dihydrochloride and lung cancer survival: Implications on metabolic re-programming

TitleTreatment with trimetazidine dihydrochloride and lung cancer survival: Implications on metabolic re-programming
Authors
KeywordsDrug repositioning
Ischemic heart disease
Lung cancer
Metabolic re-programming
Trimetazidine
Issue Date1-Nov-2024
PublisherElsevier
Citation
Lung Cancer, 2024, v. 197 How to Cite?
Abstract

Background: Metabolic re-wiring with preferential fatty acid oxidation has been observed in lung cancer cells. Whether the use of trimetazidine, an anti-anginal agent that inhibits fatty acid oxidation, alters clinical outcomes in ischemic heart disease (IHD) patients with lung cancers is unknown. Methods: We carried out this territory-wide, retrospective cohort study of 279,894 IHD patients prescribed with trimetazidine or long-acting oral nitrates in Hong Kong (population coverage of 7.5 millions, January 1999 − December 2020). A total of 6561 patients with pre-existing or de novo lung cancers were identified. Clinical outcomes of all-cause mortality were longitudinally compared between lung cancer patients who received trimetazidine (n = 547) versus non-users (control, n = 6014). Results: Over 902.9 ± 1410.6 days, lower incidence of deaths occurred in the trimetazidine group (79.0 %, n = 432/547) compared to controls (90.5 %, n = 5442/6014, P < 0.001). Kaplan-Meier analyses showed that trimetazidine use was associated with significantly higher survival from all-cause mortality in IHD patients (trimetazidine: mean survival = 1840.6 [95 %CI 1596.0–2085.3], versus control: 1056.7 [95 %CI 1011.3–1102.0] days, Log Rank = 69.4, P < 0.001). Cox regression showed that trimetazidine use was significantly associated with reduced risk of all-cause mortality in crude (HR = 0.60 [95 %CI: 0.53 to 0.68], P < 0.001) and multivariable models (HR = 0.65 [95 % CI: 0.57 to 0.74], P < 0.001). Pre-specified analyses amongst patients with pre-existing lung cancers yielded similar findings (HR = 0.49 [95 %CI: 0.35 to 0.67], P < 0.001). Survival benefits related to trimetazidine use was predominantly restricted to non-cardiovascular mortality (P < 0.001). Conclusions: Trimetazidine use is associated with higher overall survival in IHD patients with lung cancers, particularly from non-cardiovascular death. These findings need to be confirmed by randomized controlled trials.


Persistent Identifierhttp://hdl.handle.net/10722/353493
ISSN
2023 Impact Factor: 4.5
2023 SCImago Journal Rankings: 1.761
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChan, Yap-Hang-
dc.contributor.authorCheng, Yuen-Ting-
dc.contributor.authorSin, Chun-Fung-
dc.contributor.authorMa, Edmond S.K.-
dc.contributor.authorLam, Stephen T.S.-
dc.contributor.authorAu Yeung, Shiu-Lun-
dc.contributor.authorCheung, Bernard M.Y.-
dc.contributor.authorHo, Chung-Man-
dc.contributor.authorYiu, Kai-Hang-
dc.contributor.authorTse, Hung-Fat-
dc.date.accessioned2025-01-18T00:35:26Z-
dc.date.available2025-01-18T00:35:26Z-
dc.date.issued2024-11-01-
dc.identifier.citationLung Cancer, 2024, v. 197-
dc.identifier.issn0169-5002-
dc.identifier.urihttp://hdl.handle.net/10722/353493-
dc.description.abstract<p>Background: Metabolic re-wiring with preferential fatty acid oxidation has been observed in lung cancer cells. Whether the use of trimetazidine, an anti-anginal agent that inhibits fatty acid oxidation, alters clinical outcomes in ischemic heart disease (IHD) patients with lung cancers is unknown. Methods: We carried out this territory-wide, retrospective cohort study of 279,894 IHD patients prescribed with trimetazidine or long-acting oral nitrates in Hong Kong (population coverage of 7.5 millions, January 1999 − December 2020). A total of 6561 patients with pre-existing or de novo lung cancers were identified. Clinical outcomes of all-cause mortality were longitudinally compared between lung cancer patients who received trimetazidine (n = 547) versus non-users (control, n = 6014). Results: Over 902.9 ± 1410.6 days, lower incidence of deaths occurred in the trimetazidine group (79.0 %, n = 432/547) compared to controls (90.5 %, n = 5442/6014, P < 0.001). Kaplan-Meier analyses showed that trimetazidine use was associated with significantly higher survival from all-cause mortality in IHD patients (trimetazidine: mean survival = 1840.6 [95 %CI 1596.0–2085.3], versus control: 1056.7 [95 %CI 1011.3–1102.0] days, Log Rank = 69.4, P < 0.001). Cox regression showed that trimetazidine use was significantly associated with reduced risk of all-cause mortality in crude (HR = 0.60 [95 %CI: 0.53 to 0.68], P < 0.001) and multivariable models (HR = 0.65 [95 % CI: 0.57 to 0.74], P < 0.001). Pre-specified analyses amongst patients with pre-existing lung cancers yielded similar findings (HR = 0.49 [95 %CI: 0.35 to 0.67], P < 0.001). Survival benefits related to trimetazidine use was predominantly restricted to non-cardiovascular mortality (P < 0.001). Conclusions: Trimetazidine use is associated with higher overall survival in IHD patients with lung cancers, particularly from non-cardiovascular death. These findings need to be confirmed by randomized controlled trials.<br></p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofLung Cancer-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectDrug repositioning-
dc.subjectIschemic heart disease-
dc.subjectLung cancer-
dc.subjectMetabolic re-programming-
dc.subjectTrimetazidine-
dc.titleTreatment with trimetazidine dihydrochloride and lung cancer survival: Implications on metabolic re-programming -
dc.typeArticle-
dc.identifier.doi10.1016/j.lungcan.2024.107996-
dc.identifier.scopuseid_2-s2.0-85206996331-
dc.identifier.volume197-
dc.identifier.eissn1872-8332-
dc.identifier.isiWOS:001346621600001-
dc.identifier.issnl0169-5002-

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