Mortality and incidence of cancer during 10-year follow-up of the Scandinavian Simvastatin Survival Study (4S)

被引:274
作者
Strandberg, TE
Pyörälä, K
Cook, TJ
Wilhelmsen, L
Faergeman, O
Thorgeirsson, G
Pedersen, TR
Kjekshus, J
机构
[1] Univ Helsinki, Dept Med, Helsinki 00029, Finland
[2] Kuopio Univ Hosp, Dept Med, SF-70210 Kuopio, Finland
[3] Merck Res Labs, Rahway, NJ USA
[4] Univ Gothenburg, Cardiovasc Inst, Gothenburg, Sweden
[5] Arhus Univ Hosp, Aarhus, Denmark
[6] Landspitalinn Univ Hosp, Reykjavik, Iceland
[7] Ullevaal Univ Hosp, Ctr Prevent Med, Oslo, Norway
[8] Univ Oslo, Rikshosp Univ Hosp, Dept Cardiol, Oslo, Norway
关键词
D O I
10.1016/S0140-6736(04)16936-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The effects of cholesterol-lowering treatment with statins on mortality and risk of cancer beyond the usual 5-6-year trial periods are unknown. We extended post-trial follow-up of participants in the Scandinavian Simvastatin Survival Study (4S) to investigate cause-specific mortality and incidence of cancer 5 years after closure of 14 the trial. Methods 4S was a randomised double-blind trial of simivastatin or placebo in patients with coronary heart disease, serum total cholesterol 5.5-8.0 mmol/L, and serum triglycerides 2.5 mmol/L or lower. The double-blind period lasted for a median of 5.4 years (range for survivors 4.9-6.3) and ended in 1994. After the trial, most patients in both groups received open-label lipid-lowering treatment. National registers were used to assess mortality and causes of death and cancer incidence in the original treatment groups for a median total follow-up time of 10.4 years (range for survivors 9.9-11.3). Analysis was by intention to treat. Findings 414 patients originally allocated simvastatin and 468 assigned placebo died during the 10.4-year follow-up (relative risk 0.85 [95% CI 0.74-0.97], p=0.02), a difference largely attributable to lower coronary mortality in the simvastatin group (238 vs 300 deaths; 0.76 [0.64-0.90], p=0.0018). 85 cancer deaths arose in the simvastatin group versus 100 in the placebo group (0.81 [0.60-1.08], p=0.14), and 227 incident cancers were reported in the simvastin group versus 248 in the placebo group (0.88 [0.73-1.05], p=0.15). Incidence of any specific type of cancer did not A rise in the simvastatin group. Interpretation Simvastatin treatment for 5 years in a placebo-controlled trial, followed by open-label statin therapy, was associated with survival benefit over 10 years of follow-up compared with open-label statin therapy for the past 5 years only. No difference was noted in mortality from and incidence of cancer between the original simvastatin group and placebo group.
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页码:771 / 777
页数:7
相关论文
共 20 条
  • [1] Do statins cause cancer? A meta-analysis of large randomized clinical trials
    Bjerre, LM
    LeLorier, J
    [J]. AMERICAN JOURNAL OF MEDICINE, 2001, 110 (09) : 716 - 723
  • [2] Statin effects beyond lipid lowering-are they clinically relevant?
    Bonetti, PO
    Lerman, LO
    Napoli, C
    Lerman, A
    [J]. EUROPEAN HEART JOURNAL, 2003, 24 (03) : 225 - 248
  • [3] Collins R, 2002, LANCET, V360, P7, DOI 10.1016/S0140-6736(02)09327-3
  • [4] Primary prevention of acute coronary events with lovastatin in men and women with average cholesterol levels - Results of AFCAPS/TexCAPS
    Downs, JR
    Clearfield, M
    Weis, S
    Whitney, E
    Shapiro, DR
    Beere, PA
    Langendorfer, A
    Stein, EA
    Kruyer, W
    Gotto, AM
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 279 (20): : 1615 - 1622
  • [5] ENGELAND A, 1995, APMIS S, V45, P1
  • [6] Statins and cancer: A case of meta-uncertainty
    Guallar, E
    Goodman, SN
    [J]. AMERICAN JOURNAL OF MEDICINE, 2001, 110 (09) : 738 - 740
  • [7] Effect of fluvastatin on cardiac outcomes in renal transplant recipients:: a multicentre, randomised, placebo-controlled trial
    Holdaas, H
    Fellström, B
    Jardine, AG
    Holme, I
    Nyberg, G
    Fauchald, P
    Grönhagen-Riska, C
    Madsen, S
    Neumayer, HH
    Cole, E
    Maes, B
    Ambühl, P
    Olsson, AG
    Hartmann, A
    Solbu, DO
    Pedersen, TR
    [J]. LANCET, 2003, 361 (9374) : 2024 - 2031
  • [8] REPORT OF THE CONFERENCE ON LOW BLOOD CHOLESTEROL - MORTALITY ASSOCIATIONS
    JACOBS, D
    BLACKBURN, H
    HIGGINS, M
    REED, D
    ISO, H
    MCMILLAN, G
    NEATON, J
    NELSON, J
    POTTER, J
    RIFKIND, B
    ROSSOUW, J
    SHEKELLE, R
    YUSUF, S
    [J]. CIRCULATION, 1992, 86 (03) : 1046 - 1060
  • [9] Quantifying effect of statins on low density lipoprotein cholesterol, ischaemic heart disease, and stroke: systematic review and meta-analysis
    Law, MR
    Wald, NJ
    Rudnicka, AR
    [J]. BRITISH MEDICAL JOURNAL, 2003, 326 (7404): : 1423 - 1427
  • [10] Carcinogenicity of lipid-lowering drugs
    Newman, TB
    Hulley, SB
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 275 (01): : 55 - 60