The beta-carotene and retinol efficacy trial:: Incidence of lung cancer and cardiovascular disease mortality during 6-year follow-up after stopping β-carotene and retinol supplements

被引:280
作者
Goodman, GE
Thornquist, MD
Balmes, J
Cullen, MR
Meyskens, FL
Omenn, GS
Valanis, B
Williams, JH
机构
[1] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
[2] Swedish Canc Inst, Seattle, WA USA
[3] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[4] Yale Univ, Yale Sch Med, New Haven, CT USA
[5] Univ Calif Irvine, Med Ctr, Orange, CA USA
[6] Univ Michigan, Sch Med, Ann Arbor, MI 48109 USA
[7] Kaiser Permanente Ctr Hlth Res, Portland, OR USA
关键词
D O I
10.1093/jnci/djh320
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The Beta-Carotene and Retinol Efficacy Trial (CARET) tested the effect of daily beta-carotene (30 mg) and retinyl palmitate (25 000 IU) on the incidence of lung cancer, other cancers, and death in 18 314 participants who were at high risk for lung cancer because of a history of smoking or asbestos exposure. CARET was stopped ahead of schedule in January 1996 because participants who were randomly assigned to receive the active intervention were found to have a 28% increase in incidence of lung cancer, a 17% increase in incidence of death and a higher rate of cardiovascular disease mortality compared with participants in the placebo group. Methods: After the intervention ended, CARET participants returned the study vitamins to their study center and provided a final blood sample. They continue to be followed annually by telephone and mail self-report. Self-reported cancer endpoints were confirmed by review of pathology reports, and death endpoints were confirmed by review of death certificates. All statistical tests were two-sided. Results: With follow-up through December 31, 2001, the post-intervention relative risks of lung cancer and all-cause mortality for the active intervention group compared with the placebo group were 1.12 (95% confidence interval [CI] = 0.97 to 1.31) and 1.08 (95% CI = 0.99 to 1.17), respectively. Smoothed relative risk curves for lung cancer incidence and all-cause mortality indicated that relative risks remained above 1.0 throughout the post-intervention follow-up. By contrast, the relative risk of cardiovascular disease mortality decreased rapidly to 1.0 after the intervention was stopped. During the post-intervention phase, females had larger relative risks of lung cancer mortality (1.33 versus 1.14; P.36), cardiovascular disease mortality (1.44 versus 0.93; P.03), and all-cause mortality (1.37 versus 0.98; P = .001) than males. Conclusions: The previously reported adverse effects of P-carotene and retinyl palmitate on lung cancer incidence and all-cause mortality in cigarette smokers and individuals with occupational exposure to asbestos persisted after drug administration was stopped although they are no longer statistically significant. Planned subgroup analyses suggest that the excess risks of lung cancer were restricted primarily to females, and cardiovascular disease mortality primarily to females and to former smokers.
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页码:1743 / 1750
页数:8
相关论文
共 34 条
[1]   alpha-tocopherol and beta-carotene supplements and lung cancer incidence in the Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study: Effects of base-line characteristics and study compliance [J].
Albanes, D ;
Heinonen, OP ;
Taylor, PR ;
Virtamo, J ;
Edwards, BK ;
Rautalahti, M ;
Hartman, AM ;
Palmgren, J ;
Freedman, LS ;
Haapakoski, J ;
Barrett, MJ ;
Pietinen, P ;
Malila, N ;
Tala, E ;
Liippo, K ;
Salomaa, ER ;
Tangrea, JA ;
Teppo, L ;
Askin, FB ;
Taskinen, E ;
Erozan, Y ;
Greenwald, P ;
Huttunen, JK .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (21) :1560-1570
[2]   Women and lung cancer - Waiting to exhale [J].
Baldini, EH ;
Strauss, GM .
CHEST, 1997, 112 (04) :S229-S234
[3]   Stopping the active intervention: CARET [J].
Bowen, DJ ;
Thornquist, M ;
Anderson, K ;
Barnett, M ;
Powell, C ;
Goodman, G ;
Omenn, G .
CONTROLLED CLINICAL TRIALS, 2003, 24 (01) :39-50
[4]   GENDER AND HISTOLOGIC TYPE VARIATIONS IN SMOKING-RELATED RISK OF LUNG-CANCER [J].
BROWNSON, RC ;
CHANG, JC ;
DAVIS, JR .
EPIDEMIOLOGY, 1992, 3 (01) :61-64
[5]  
Cavalieri E, 2000, J Natl Cancer Inst Monogr, P75
[6]  
GOODMAN GE, 1993, CANCER EPIDEM BIOMAR, V2, P389
[7]  
HEINONEN OP, 1994, NEW ENGL J MED, V330, P1029
[8]   Lack of effect of long-term supplementation with beta carotene on the incidence of malignant neoplasms and cardiovascular disease [J].
Hennekens, CH ;
Buring, JE ;
Manson, JE ;
Stampfer, M ;
Rosner, B ;
Cook, NR ;
Belanger, C ;
LaMotte, F ;
Gaziano, JM ;
Ridker, PM ;
Willett, W ;
Peto, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (18) :1145-1149
[9]   Cancer statistics, 2003 [J].
Jemal, A ;
Murray, T ;
Samuels, A ;
Ghafoor, A ;
Ward, E ;
Thun, MJ .
CA-A CANCER JOURNAL FOR CLINICIANS, 2003, 53 (01) :5-26
[10]   CARCINOMA OF THE LUNG IN WOMEN [J].
KIRSH, MM ;
TASHIAN, J ;
SLOAN, H .
ANNALS OF THORACIC SURGERY, 1982, 34 (01) :34-39