Frequency of cancer events with saxagliptin in the SAVOR-TIMI 53 trial

被引:32
作者
Leiter, L. A. [1 ]
Teoh, H. [1 ,2 ,3 ]
Mosenzon, O. [4 ]
Cahn, A. [4 ]
Hirshberg, B. [5 ]
Stahre, C. A. M. [6 ]
Hoekstra, J. B. L. [7 ]
Alvarsson, M. [8 ]
Im, K. [9 ]
Scirica, B. M. [9 ]
Bhatt, D. L. [9 ]
Raz, I. [4 ]
机构
[1] Univ Toronto, Div Endocrinol & Metab, Li Ka Shing Knowledge Inst, St Michaels Hosp, Toronto, ON, Canada
[2] Li Ka Shing Knowledge Inst, Div Cardiac Surg, Toronto, ON, Canada
[3] St Michaels Hosp, Keenan Res Ctr Biomed Sci, 30 Bond St, Toronto, ON M5B 1W8, Canada
[4] Hadassah Hebrew Univ, Med Ctr, Diabetes Unit, Div Internal Med, Jerusalem, Israel
[5] AstraZeneca, Wilmington, DE USA
[6] AstraZeneca, Molndal, Sweden
[7] Univ Amsterdam, Internal Med, Amsterdam, Netherlands
[8] Karolinska Inst Solna, Mol Med & Surg, Endocrinol Metab & Diabet, Stockholm, Sweden
[9] Harvard Univ, Brigham & Womens Hosp, Sch Med, TIMI Study Grp,Cardiovasc Div, Boston, MA 02115 USA
关键词
antihyperglycemic agents; cancer; saxagliptin; RISK; METAANALYSIS; METFORMIN; PEOPLE;
D O I
10.1111/dom.12582
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Saxagliptin Assessment of Vascular Outcomes Recorded in Patients with Diabetes Mellitus (SAVOR)-Thrombolysis in Myocardial Infarction (TIMI) 53 trial randomized trial of 16 492 patients (placebo, n = 8212; saxagliptin, n = 8280) treated and followed for a median of 2.1 years afforded an opportunity to explore whether there was any association with cancer reported as a serious adverse event. At least one cancer event was reported by 688 patients (4.1%): 362 (4.3%) and 326 (3.8%) in the placebo and saxagliptin arms, respectively (p = 0.13). There were 59 (0.6%) deaths adjudicated as malignancy deaths with placebo and 53 (0.6%) with saxagliptin. Stratification by gender, age, race and ethnicity, diabetes duration, baseline glycated haemoglobin and pharmacotherapy did not show any clinically meaningful differences between the two study arms. The overall number of cancer events and malignancy-associated mortality rates were generally balanced between the placebo and saxagliptin groups, suggesting a null relationship with saxagliptin use over the median follow-up of 2.1 years. Multivariable modelling showed that male gender, dyslipidaemia and current smoking were independent predictors of cancer. These randomized data with adequate numbers of cancer cases are reassuring but limited, by the short follow-up in a trial not designed to test this hypothesis.
引用
收藏
页码:186 / 190
页数:5
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