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Article: Treatment with trimetazidine dihydrochloride and lung cancer survival: Implications on metabolic re-programming
Title | Treatment with trimetazidine dihydrochloride and lung cancer survival: Implications on metabolic re-programming |
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Authors | |
Keywords | Drug repositioning Ischemic heart disease Lung cancer Metabolic re-programming Trimetazidine |
Issue Date | 1-Nov-2024 |
Publisher | Elsevier |
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 Identifier | http://hdl.handle.net/10722/353493 |
ISSN | 2023 Impact Factor: 4.5 2023 SCImago Journal Rankings: 1.761 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Chan, Yap-Hang | - |
dc.contributor.author | Cheng, Yuen-Ting | - |
dc.contributor.author | Sin, Chun-Fung | - |
dc.contributor.author | Ma, Edmond S.K. | - |
dc.contributor.author | Lam, Stephen T.S. | - |
dc.contributor.author | Au Yeung, Shiu-Lun | - |
dc.contributor.author | Cheung, Bernard M.Y. | - |
dc.contributor.author | Ho, Chung-Man | - |
dc.contributor.author | Yiu, Kai-Hang | - |
dc.contributor.author | Tse, Hung-Fat | - |
dc.date.accessioned | 2025-01-18T00:35:26Z | - |
dc.date.available | 2025-01-18T00:35:26Z | - |
dc.date.issued | 2024-11-01 | - |
dc.identifier.citation | Lung Cancer, 2024, v. 197 | - |
dc.identifier.issn | 0169-5002 | - |
dc.identifier.uri | http://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.language | eng | - |
dc.publisher | Elsevier | - |
dc.relation.ispartof | Lung Cancer | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Drug repositioning | - |
dc.subject | Ischemic heart disease | - |
dc.subject | Lung cancer | - |
dc.subject | Metabolic re-programming | - |
dc.subject | Trimetazidine | - |
dc.title | Treatment with trimetazidine dihydrochloride and lung cancer survival: Implications on metabolic re-programming | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.lungcan.2024.107996 | - |
dc.identifier.scopus | eid_2-s2.0-85206996331 | - |
dc.identifier.volume | 197 | - |
dc.identifier.eissn | 1872-8332 | - |
dc.identifier.isi | WOS:001346621600001 | - |
dc.identifier.issnl | 0169-5002 | - |