Hormone replacement therapy and the risk of endometrial cancer: A systematic review

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Standard

Hormone replacement therapy and the risk of endometrial cancer : A systematic review. / Sjögren, Lea L; Mørch, Lina Steinrud; Løkkegaard, Ellen.

I: Maturitas, Bind 91, 09.2016, s. 25-35.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Sjögren, LL, Mørch, LS & Løkkegaard, E 2016, 'Hormone replacement therapy and the risk of endometrial cancer: A systematic review', Maturitas, bind 91, s. 25-35. https://doi.org/10.1016/j.maturitas.2016.05.013

APA

Sjögren, L. L., Mørch, L. S., & Løkkegaard, E. (2016). Hormone replacement therapy and the risk of endometrial cancer: A systematic review. Maturitas, 91, 25-35. https://doi.org/10.1016/j.maturitas.2016.05.013

Vancouver

Sjögren LL, Mørch LS, Løkkegaard E. Hormone replacement therapy and the risk of endometrial cancer: A systematic review. Maturitas. 2016 sep.;91:25-35. https://doi.org/10.1016/j.maturitas.2016.05.013

Author

Sjögren, Lea L ; Mørch, Lina Steinrud ; Løkkegaard, Ellen. / Hormone replacement therapy and the risk of endometrial cancer : A systematic review. I: Maturitas. 2016 ; Bind 91. s. 25-35.

Bibtex

@article{7e0c894bbed44b49a70462c12caee925,
title = "Hormone replacement therapy and the risk of endometrial cancer: A systematic review",
abstract = "BACKGROUND: In 1975, estrogen only was found to be associated with an increased risk of endometrial cancer. In November 2015, NICE guidelines on hormone therapy were published that did not take this risk into account.AIM: This systematic literature review assesses the safety of estrogen plus progestin therapy according to the risk of endometrial cancer, while considering both regimen and type of progestin.METHODS: PubMed, EMBASE and the Cochrane Library were searched, resulting in the identification of 527 published articles on menopausal women with intact uteri treated with estrogen only, estrogen plus progestin or tibolone for a minimum of one year. Risk of endometrial cancer was compared to placebo or never users and measured as relative risk, hazard or odds ratio.RESULTS: 28 studies were included. The observational literature found an increased risk among users of estrogen alone. Continuous combined therapy showed a lower risk than sequential combined therapy. The newer marketed micronized progesterone increased the risk notably, also when administered continuously. In most studies, tibolone was associated with an increased risk.CONCLUSION: Use of unopposed estrogen, tibolone and sequential combined therapy increases the risk of endometrial cancer. Continuous combined therapy seems risk free, but possibly not when micronized progesterone is used.",
keywords = "Endometrial Neoplasms, Estrogen Replacement Therapy, Estrogens, Female, Humans, Middle Aged, Odds Ratio, Postmenopause, Practice Guidelines as Topic, Progestins, Risk Factors, Journal Article, Review",
author = "Sj{\"o}gren, {Lea L} and M{\o}rch, {Lina Steinrud} and Ellen L{\o}kkegaard",
note = "Copyright {\textcopyright} 2016 Elsevier Ireland Ltd. All rights reserved.",
year = "2016",
month = sep,
doi = "10.1016/j.maturitas.2016.05.013",
language = "English",
volume = "91",
pages = "25--35",
journal = "Maturitas",
issn = "0378-5122",
publisher = "Elsevier Ireland Ltd",

}

RIS

TY - JOUR

T1 - Hormone replacement therapy and the risk of endometrial cancer

T2 - A systematic review

AU - Sjögren, Lea L

AU - Mørch, Lina Steinrud

AU - Løkkegaard, Ellen

N1 - Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

PY - 2016/9

Y1 - 2016/9

N2 - BACKGROUND: In 1975, estrogen only was found to be associated with an increased risk of endometrial cancer. In November 2015, NICE guidelines on hormone therapy were published that did not take this risk into account.AIM: This systematic literature review assesses the safety of estrogen plus progestin therapy according to the risk of endometrial cancer, while considering both regimen and type of progestin.METHODS: PubMed, EMBASE and the Cochrane Library were searched, resulting in the identification of 527 published articles on menopausal women with intact uteri treated with estrogen only, estrogen plus progestin or tibolone for a minimum of one year. Risk of endometrial cancer was compared to placebo or never users and measured as relative risk, hazard or odds ratio.RESULTS: 28 studies were included. The observational literature found an increased risk among users of estrogen alone. Continuous combined therapy showed a lower risk than sequential combined therapy. The newer marketed micronized progesterone increased the risk notably, also when administered continuously. In most studies, tibolone was associated with an increased risk.CONCLUSION: Use of unopposed estrogen, tibolone and sequential combined therapy increases the risk of endometrial cancer. Continuous combined therapy seems risk free, but possibly not when micronized progesterone is used.

AB - BACKGROUND: In 1975, estrogen only was found to be associated with an increased risk of endometrial cancer. In November 2015, NICE guidelines on hormone therapy were published that did not take this risk into account.AIM: This systematic literature review assesses the safety of estrogen plus progestin therapy according to the risk of endometrial cancer, while considering both regimen and type of progestin.METHODS: PubMed, EMBASE and the Cochrane Library were searched, resulting in the identification of 527 published articles on menopausal women with intact uteri treated with estrogen only, estrogen plus progestin or tibolone for a minimum of one year. Risk of endometrial cancer was compared to placebo or never users and measured as relative risk, hazard or odds ratio.RESULTS: 28 studies were included. The observational literature found an increased risk among users of estrogen alone. Continuous combined therapy showed a lower risk than sequential combined therapy. The newer marketed micronized progesterone increased the risk notably, also when administered continuously. In most studies, tibolone was associated with an increased risk.CONCLUSION: Use of unopposed estrogen, tibolone and sequential combined therapy increases the risk of endometrial cancer. Continuous combined therapy seems risk free, but possibly not when micronized progesterone is used.

KW - Endometrial Neoplasms

KW - Estrogen Replacement Therapy

KW - Estrogens

KW - Female

KW - Humans

KW - Middle Aged

KW - Odds Ratio

KW - Postmenopause

KW - Practice Guidelines as Topic

KW - Progestins

KW - Risk Factors

KW - Journal Article

KW - Review

U2 - 10.1016/j.maturitas.2016.05.013

DO - 10.1016/j.maturitas.2016.05.013

M3 - Review

C2 - 27451318

VL - 91

SP - 25

EP - 35

JO - Maturitas

JF - Maturitas

SN - 0378-5122

ER -

ID: 177062959