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Hormonal contraception and risk of endometrial cancer: a systematic review.
Endocr Relat Cancer 2010; 17(4):R263-71ER

Abstract

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  μg/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.

Authors+Show Affiliations

Department of Endocrinology and Menopause, Centre for Women's Health BW, University Women's Hospital, Calwer Strasse 7, D-72076 Tuebingen, Germany. alfred.mueck@med.uni-tuebingen.deNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Review
Systematic Review

Language

eng

PubMed ID

20870686

Citation

Mueck, Alfred O., et al. "Hormonal Contraception and Risk of Endometrial Cancer: a Systematic Review." Endocrine-related Cancer, vol. 17, no. 4, 2010, pp. R263-71.
Mueck AO, Seeger H, Rabe T. Hormonal contraception and risk of endometrial cancer: a systematic review. Endocr Relat Cancer. 2010;17(4):R263-71.
Mueck, A. O., Seeger, H., & Rabe, T. (2010). Hormonal contraception and risk of endometrial cancer: a systematic review. Endocrine-related Cancer, 17(4), pp. R263-71. doi:10.1677/ERC-10-0076.
Mueck AO, Seeger H, Rabe T. Hormonal Contraception and Risk of Endometrial Cancer: a Systematic Review. Endocr Relat Cancer. 2010;17(4):R263-71. PubMed PMID: 20870686.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Hormonal contraception and risk of endometrial cancer: a systematic review. AU - Mueck,Alfred O, AU - Seeger,Harald, AU - Rabe,Thomas, Y1 - 2010/09/23/ PY - 2010/9/28/entrez PY - 2010/9/28/pubmed PY - 2011/1/8/medline SP - R263 EP - 71 JF - Endocrine-related cancer JO - Endocr. Relat. Cancer VL - 17 IS - 4 N2 - 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  μg/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. SN - 1479-6821 UR - http://www.unboundmedicine.com/medline/citation/20870686/full_citation L2 - https://erc.bioscientifica.com/doi/10.1677/ERC-10-0076 DB - PRIME DP - Unbound Medicine ER -