Loading…

Depot medroxyprogesterone acetate and endometrial cancer: A multicenter case–control study

Objective To assess the associations between depot medroxyprogesterone acetate (DMPA) and endometrial cancer. Methods This multicenter case–control study was conducted among tertiary hospitals in Thailand. Patients were women with endometrial cancer. Controls were women admitted for other conditions...

Full description

Saved in:
Bibliographic Details
Published in:International journal of gynecology and obstetrics 2023-10, Vol.163 (1), p.96-102
Main Authors: Kietpeerakool, Chumnan, Cheewakriangkrai, Chalong, Rattanakanokchai, Siwanon, Rattanalappaiboon, Daungporn, Tiyayon, Jitima, Chalapati, Wadwilai, Tangsiriwattana, Thumwadee, Tangjitgamol, Siriwan, Kleebkaow, Pilaiwan, Khunamornpong, Surapan, Temtanakitpaisan, Amornrat, Sribanditmongkhol, Narisa, Lumbiganon, Pisake
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Objective To assess the associations between depot medroxyprogesterone acetate (DMPA) and endometrial cancer. Methods This multicenter case–control study was conducted among tertiary hospitals in Thailand. Patients were women with endometrial cancer. Controls were women admitted for other conditions, matched for age within 5 years of the patients' age. The controls had to have no abnormal vaginal bleeding, history of hysterectomy, or cancers of the other organs. A standardized questionnaire was used to gather information. Conditional logistic regression was applied to calculate adjusted odds ratio (aORs) and 95% confidence intervals (CIs). Results During 2015 to 2021, 378 patients and 1134 controls were included. Ever use of DMPA was associated with a 70% decreased overall risk of endometrial cancer (aOR, 0.30 [95% CI, 0.21–0.42]). Endometrial cancer risk declined by 3% (aOR, 0.97 [95% CI, 0.96–0.98]) for every 3 months of DMPA use. The magnitude of the decline in endometrial cancer risk did not vary appreciably by cancer subtypes (aOR, 0.26 [95% CI, 0.17–0.41] and 0.38 [95% CI, 0.22–0.65] for low‐grade and high‐grade tumors, respectively). Conclusions Depot medroxyprogesterone acetate use was inversely associated with endometrial cancer risk in a duration‐dependent manner. This association was independent of cancer subtype. Synopsis Depot medroxyprogesterone acetate use was independently associated with a reduced risk of endometrial cancer.
ISSN:0020-7292
1879-3479
1879-3479
DOI:10.1002/ijgo.14846