Hormonal contraception and risk of endometrial cancer: a systematic review

被引:56
作者
Mueck, Alfred O. [1 ]
Seeger, Harald [1 ]
Rabe, Thomas [1 ]
机构
[1] Univ Womens Hosp, Dept Endocrinol & Menopause, Ctr Womens Hlth BW, D-72076 Tubingen, Germany
关键词
LEVONORGESTREL INTRAUTERINE SYSTEM; PRACTITIONERS ORAL-CONTRACEPTION; RANDOMIZED CONTROLLED-TRIAL; TERM-FOLLOW-UP; REPLACEMENT THERAPY; DEVICE USE; MEDROXYPROGESTERONE ACETATE; ROYAL-COLLEGE; GENITAL-TRACT; LNG-IUS;
D O I
10.1677/ERC-10-0076
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
More than 15 case-control studies and at least four large cohort studies demonstrated a decrease in the risk of endometrial cancer of about 50% for ever use of combined oral contraceptives (COCs). In most of these studies, this protective effect persisted for more than 10-15-20 years after cessation of the COC. An increasing protective effect with longer duration of COC use has been found in most studies. The beneficial effect was independent of the composition of COC, i.e. dosage and type of progestogen, combined with ethinyl estradiol 30-50 mu g/day. COCs with higher progestogen potency seem to be somewhat more effective. Nonhormonal uterine devices have also been found to be strongly protective; however, data on oral or injectable progestogen-only preparations (POPs) including the levonorgestrel-releasing intrauterine system (LNG-IUS) are still rare, but also suggest similar protective action. COCs, POPs, as well as LNG-IUS can effectively reduce endometrial hyperplasia but should only be used in exceptional cases in patients with or after endometrial cancer. In contrast to nonhormonal IUS, systemic side effects cannot be excluded with LNG-IUS, but they are certainly rare, as the main effect has decreased the endometrial estrogen response because of the high endometrial tissue levels of LNG. Endocrine-Related Cancer (2010) 17 R263-R271
引用
收藏
页码:R263 / R271
页数:9
相关论文
共 55 条
[1]  
AIKAT M, 1980, INDIAN J MED RES, V71, P879
[2]   Meta-analysis of intrauterine device use and risk of endometrial cancer [J].
Beining, Robin M. ;
Dennis, Leslie K. ;
Smith, Elaine M. ;
Dokras, Anuja .
ANNALS OF EPIDEMIOLOGY, 2008, 18 (06) :492-499
[3]  
BERAL V, 1988, LANCET, V2, P1331
[4]  
BRINTON LA, 1993, OBSTET GYNECOL, V81, P265
[5]   INTRAUTERINE CONTRACEPTION AND THE RISK OF ENDOMETRIAL CANCER [J].
CASTELLSAGUE, X ;
THOMPSON, WD ;
DUBROW, R .
INTERNATIONAL JOURNAL OF CANCER, 1993, 54 (06) :911-916
[6]   A randomised controlled trial of prophylactic levonorgestrel intrauterine system in tamoxifen-treated women [J].
Chan, S. S. C. ;
Tam, W. H. ;
Yeo, W. ;
Yu, M. M. Y. ;
Ng, D. P. S. ;
Wong, A. W. Y. ;
Kwan, W. H. ;
Yuena, P. M. .
BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 2007, 114 (12) :1510-1515
[7]   Is levonorgestrel intrauterine system effective for treatment of early endometrial cancer? Report of four cases and review of the literature [J].
Dhar, KK ;
NeedhiRajan, T ;
Koslowski, A ;
Woolas, RP .
GYNECOLOGIC ONCOLOGY, 2005, 97 (03) :924-927
[8]   Endometrial protection from tamoxifen-stimulated changes by a levonorgestrel-releasing intrauterine system: a randomised controlled trial [J].
Gardner, FJE ;
Konje, JC ;
Abrams, KR ;
Brown, LJR ;
Khanna, S ;
Al-Azzawi, F ;
Bell, SC ;
Taylor, DJ .
LANCET, 2000, 356 (9243) :1711-1717
[9]   Levonorgestrel-releasing intrauterine system (LNG-IUS) as a therapy for endometrial carcinoma [J].
Giannopoulos, T ;
Butler-Manuel, S ;
Tailor, A .
GYNECOLOGIC ONCOLOGY, 2004, 95 (03) :762-764
[10]   PRIMARY PREVENTION OF GYNECOLOGIC CANCERS [J].
GRIMES, DA ;
ECONOMY, KE .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1995, 172 (01) :227-235