The Association of Sodium-Glucose Cotransporter 2 Inhibitors With Cardiovascular Outcomes in Anthracycline-Treated Patients With Cancer

被引:51
作者
Abdel-Qadir, Husam [1 ,2 ,3 ,4 ,5 ,6 ]
Carrasco, Rodrigo [6 ]
Austin, Peter C. [4 ,5 ]
Chen, Yue [7 ]
Zhou, Limei [3 ]
Fang, Jiming [3 ]
Su, Henry M. H. [6 ]
Lega, Iliana C. [1 ,3 ,4 ,5 ]
Kaul, Padma [8 ,9 ]
Neilan, Tomas G. [10 ]
Thavendiranathan, Paaladinesh [5 ,6 ,11 ]
机构
[1] Womens Coll Hosp, Room 6452,76 Grenville St, Toronto, ON M5S 1B2, Canada
[2] Univ Hlth Network, Toronto, ON, Canada
[3] ICES, Inst Clin Evaluat Sci, Toronto, ON, Canada
[4] Univ Toronto, Inst Hlth Policy Management & Evaluat, Toronto, ON, Canada
[5] Univ Toronto, Dept Med, Toronto, ON, Canada
[6] Univ Hlth Network, Ted Rogers Program Cardiotox Prevent, Toronto, ON, Canada
[7] Univ Ottawa, Fac Med, Sch Epidemiol & Publ Hlth, Ottawa, ON, Canada
[8] Univ Alberta, Dept Med, Edmonton, AB, Canada
[9] Univ Alberta, Global Collaborat Cardiovasc Res Ctr, Canadian Virtual Coordinating Ctr, Edmonton, AB, Canada
[10] Massachusetts Gen Hosp, Boston, MA USA
[11] Univ Toronto, Toronto Gen Hosp, Peter Munk Cardiac Ctr, Ted Rogers Program Cardiotox Prevent, 585 Univ Ave, Toronto, ON M5G2 2N2, Canada
关键词
anthracyclines; cardio-oncology; cardiotoxicity; heart failure; sodium-glucose transport protein 2; RNA-SEQ; SERUM HAPTOGLOBIN; 5-YEAR SURVIVORS; LATE MORTALITY; HEART-FAILURE; CHILDHOOD; GENE; HP; CARDIOTOXICITY; CARDIOMYOPATHY;
D O I
10.1016/j.jaccao.2023.03.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND Sodium glucose cotransporter-2 inhibitors (SGLT2is) are hypothesized to reduce the risk of anthracycline-associated cardiotoxicity.OBJECTIVES This study sought to determine the association between SGLT2is and cardiovascular disease (CVD) after anthracycline-containing chemotherapy.METHODS Using administrative data sets, we conducted a population-based cohort study of people >65 years of age with treated diabetes and no prior heart failure (HF) who received anthracyclines between January 1, 2016, and December 31, 2019. After estimating propensity scores for SGLT2i use, the average treatment effects for the treated weights were used to reduce baseline differences between SGLT2i-exposed and-unexposed controls. The outcomes were hospitali-zation for HF, incident HF diagnoses (in-or out-of-hospital), and documentation of any CVD in future hospitalizations. Death was treated as a competing risk. Cause-specific HRs for each outcome were determined for SGLT2i-treated people relative to unexposed controls.RESULTS We studied 933 patients (median age 71.0 years, 62.2% female), 99 of whom were SGLT2i treated. During a median follow-up of 1.6 years, there were 31 hospitalizations for HF (0 in the SGLT2i group), 93 new HF diagnoses, and 74 hospitalizations with documented CVD. Relative to controls, SGLT2i exposure was associated with HR of 0 for HF hospitalization (P < 0.001) but no significant difference in incident HF diagnosis (HR: 0.55; 95% CI: 0.23-1.31; P = 0.18) or CVD diagnosis (HR: 0.39; 95% CI: 0.12-1.28; P = 0.12). There was no significant difference in mortality (HR: 0.63; 95% CI: 0.36-1.11; P = 0.11).CONCLUSIONS SGLT2is may reduce the rate of HF hospitalization after anthracycline-containing chemotherapy. This hypothesis warrants further testing in randomized controlled trials. (J Am Coll Cardiol CardioOnc 2023;5:318-328)& COPY; 2023 Published by Elsevier on behalf of the American College of Cardiology Foundation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:318 / 328
页数:138
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