Low-density lipoprotein cholesterol lowering in real-world patients treated with evolocumab

被引:8
作者
Desai, Nihar R. [1 ]
Wade, Rolin L. [2 ]
Xiang, Pin [3 ,4 ]
Pinto, Lionel [3 ]
Nunna, Sasikiran [2 ,5 ]
Wang, Xin [2 ]
Exter, Jason [3 ]
Mues, Katherine E. [3 ]
Habib, Mohdhar [3 ]
Chen, Chi-Chang [2 ]
机构
[1] Yale Sch Med, New Haven, CT 06520 USA
[2] IQVIA, Plymouth Meeting, PA USA
[3] Amgen Inc, Thousand Oaks, CA 91320 USA
[4] Boehringer Ingelheim Pharmaceut Inc, 90 E Ridge POB 368, Ridgefield, CT 06877 USA
[5] Bristol Myers Squibb Inc, Lawrenceville, NJ USA
关键词
atherosclerotic cardiovascular disease; LDL‐ C; real‐ world evidence; CORONARY-HEART-DISEASE; HIGH-RISK; CARDIOVASCULAR-DISEASE; DYSLIPIDEMIA; MORTALITY; THERAPY; NONADHERENCE; ASSOCIATION; MANAGEMENT; COUNTRIES;
D O I
10.1002/clc.23600
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Low-density lipoprotein cholesterol (LDL-C) is a risk factor for atherosclerotic cardiovascular disease (ASCVD). There are limited real-world data on LDL-C lowering with evolocumab in United States clinical practice. Hypothesis We assessed LDL-C lowering during 1 year of evolocumab therapy. Methods This retrospective cohort study used linked laboratory (Prognos) and medical claims (IQVIA Dx/LRx and PharMetrics Plus(R)) data. Patients with a first fill for evolocumab between 7/1/2015 and 10/31/2019 (index event) and LDL-C >= 70 mg/dL were included (overall cohort; N = 5897). Additionally, a patient subgroup with a recent myocardial infarction (MI) within 12 months (median 130 days) before the first evolocumab fill was identified (N = 152). Reduction from baseline LDL-C was calculated based on the lowest LDL-C value recorded during a 12-month follow-up period. Results The mean (SD) age was 65 (10) years; 61.9% of patients had ASCVD diagnoses and 70.7% of patients were in receipt of lipid-lowering therapy. Following evolocumab treatment, changes in LDL-C from baseline were -60% in the overall cohort (median [interquartile range (IQR)] 146 [115-180] mg/dL to 58 [36-84] mg/dL) and -65% in the recent MI subgroup (median [IQR] 137 [109-165] mg/dL to 48 [30-78] mg/dL). In the overall cohort and recent MI subgroup, 62.1% and 69.7% of patients achieved LDL-C < 70 mg/dL, respectively. Conclusions In this real-world analysis, evolocumab was associated with significant reductions in LDL-C comparable to that seen in the FOURIER clinical trial, which were durable over 1 year of treatment.
引用
收藏
页码:715 / 722
页数:8
相关论文
共 39 条
  • [1] [Anonymous], 2017, REPATHA (evolocumab) [package insert]
  • [2] Demographic And Clinical Characteristics Of Patients Prescribed Proprotein Convertase Subtilisin/kexin Type 9 Inhibitor Therapy And Patients Whose Current Lipid-Lowering Therapy Was Modified
    Baum, Seth J.
    Wade, Rolin L.
    Xiang, Pin
    Arellano, Jorge
    Olmos, Cesar Cerezo
    Nunna, Sasikiran
    Chen, Chi-Chang
    Carter, Cathryn M.
    Desai, Nihar R.
    [J]. THERAPEUTICS AND CLINICAL RISK MANAGEMENT, 2019, 15 : 1325 - 1332
  • [3] PCSK9 inhibitor access barriersissues and recommendations: Improving the access process for patients, clinicians and payers
    Baum, Seth J.
    Toth, Peter P.
    Underberg, James A.
    Jellinger, Paul
    Ross, Joyce
    Wilemon, Katherine
    [J]. CLINICAL CARDIOLOGY, 2017, 40 (04) : 243 - 254
  • [4] A 52-Week Placebo-Controlled Trial of Evolocumab in Hyperlipidemia
    Blom, Dirk J.
    Hala, Tomas
    Bolognese, Michael
    Lillestol, Michael J.
    Toth, Phillip D.
    Burgess, Lesley
    Ceska, Richard
    Roth, Eli
    Koren, Michael J.
    Ballantyne, Christie M.
    Monsalvo, Maria Laura
    Tsirtsonis, Kate
    Kim, Jae B.
    Scott, Rob
    Wasserman, Scott M.
    Stein, Evan A.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2014, 370 (19) : 1809 - 1819
  • [5] Very Low Levels of Atherogenic Lipoproteins and the Risk for Cardiovascular Events A Meta-Analysis of Statin Trials
    Boekholdt, S. Matthijs
    Hovingh, G. Kees
    Mora, Samia
    Arsenault, Benoit J.
    Amarenco, Pierre
    Pedersen, Terje R.
    LaRosa, John C.
    Waters, David D.
    DeMicco, David A.
    Simes, R. John
    Keech, Antony C.
    Colquhoun, David
    Hitman, Graham A.
    Betteridge, John
    Clearfield, Michael B.
    Downs, John R.
    Colhoun, Helen M.
    Gotto, Antonio M., Jr.
    Ridker, Paul M.
    Grundy, Scott M.
    Kastelein, John J. P.
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2014, 64 (05) : 485 - 494
  • [6] Residual risk for coronary heart disease events and mortality despite intensive medical management after myocardial infarction
    Brown, Todd M.
    Bittner, Vera
    Colantonio, Lisandro D.
    Deng, Luqin
    Farkouh, Michael E.
    Limdi, Nita
    Monda, Keri L.
    Rosenson, Robert S.
    Serban, Maria-Corina
    Somaratne, Ransi M.
    Zhao, Hong
    Woodward, Mark
    Muntner, Paul
    [J]. JOURNAL OF CLINICAL LIPIDOLOGY, 2020, 14 (02) : 260 - 270
  • [7] Suboptimal Control of Lipid Levels: Results from 29 Countries Participating in the Centralized Pan-Regional Surveys on the Undertreatment of Hypercholesterolaemia (CEPHEUS)
    Chiang, Chern-En
    Ferrieres, Jean
    Gotcheva, Nina N.
    Raal, Frederick J.
    Shehab, Abdulla
    Sung, Jidong
    Henriksson, Karin M.
    Hermans, Michel P.
    [J]. JOURNAL OF ATHEROSCLEROSIS AND THROMBOSIS, 2016, 23 (05) : 567 - 587
  • [8] Cohen JD, 2017, J CLIN LIPIDOL, V11, P891, DOI [10.1016/j.jac1.2017.04.120, 10.1016/j.jacl.2017.04.120]
  • [9] Ischemic Event Rates in Very-High-Risk Adults
    Colantonio, Lisandro D.
    Shannon, Erin D.
    Orroth, Kate K.
    Zaha, Rebecca
    Jackson, Elizabeth A.
    Rosenson, Robert S.
    Exter, Jason
    Mues, Katherine E.
    Muntner, Paul
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2019, 74 (20) : 2496 - 2507
  • [10] Adherence to High-Intensity Statins Following a Myocardial Infarction Hospitalization Among Medicare Beneficiaries
    Colantonio, Lisandro D.
    Huang, Lei
    Monda, Keri L.
    Bittner, Vera
    Serban, Maria-Corina
    Taylor, Benjamin
    Brown, Todd M.
    Glasser, Stephen P.
    Muntner, Paul
    Rosenson, Robert S.
    [J]. JAMA CARDIOLOGY, 2017, 2 (08) : 890 - 895