TY - JOUR
T1 - Depot‐medroxyprogesterone acetate (dmpa) and risk of edometrial cancer
AU - THE WHO COLLABORATIVE STUDY OF NEOPLASIA AND STEROID CONTRACEPTIVES
AU - Silpisornkosol, Suporn
AU - Pardthaisong, Tieng
AU - Sahapong, Virote
AU - Theetranont, Choti
AU - Boosiri, Banpot
AU - Chutivongse, Supawat
AU - Virutamasen, Pramuan
AU - Wongsrchanalai, Chansuda
AU - Sindhvananda, Sermsri
AU - Koetsawang, Suporn
AU - Rachawat, Daungdao
AU - Koetsawang, Amom
AU - Langley, F. A.
AU - Thomas Study Coordinator, David B.
AU - Ray, Roberta M.
AU - Noonan, Elizabeth A.
AU - Stanford, Janet L.
AU - Rosenblatt, Karin A.
AU - Holck, Susan
AU - Farley, Timothy M.M.
AU - Thomas, David B.
AU - Ray, Roberta M.
PY - 1991/9/9
Y1 - 1991/9/9
N2 - This is a report of results from a case‐control study of the relationship of the long‐acting progestational contraceptive, depot‐medroxyprogesterone acetate (DMPA) to risk of endometrial carcinoma. Prior use of DMPA and information on known and suspected risk factors for endometrial cancer were ascertained in personal interviews with 122 women with histologically confirmed disease and 939 controls selected from 2 hospitals in Bangkok and 1 in Chiang Mai, Thailand. Based on 3 exposed cases and 84 exposed controls, the relative risk of endometrial cancer was estimated to be 0.21 (95% confidence interval = 0.06,0.79) in women who had ever used DMPA (but who had not first used DMPA in the year prior to diagnosis). All 3 exposed cases had also received estrogens pre‐menopausally. Exposure to such estrogens enhanced risk of endometrial cancer and reduced the apparent protective effect of DMPA. Although based on small numbers of exposed women, the protective effect of DMPA appeared to last for at least 8 years after cessation of use. The reduction in risk of endometrial cancer is at least as great for DMPA as for combined oral contraceptives.
AB - This is a report of results from a case‐control study of the relationship of the long‐acting progestational contraceptive, depot‐medroxyprogesterone acetate (DMPA) to risk of endometrial carcinoma. Prior use of DMPA and information on known and suspected risk factors for endometrial cancer were ascertained in personal interviews with 122 women with histologically confirmed disease and 939 controls selected from 2 hospitals in Bangkok and 1 in Chiang Mai, Thailand. Based on 3 exposed cases and 84 exposed controls, the relative risk of endometrial cancer was estimated to be 0.21 (95% confidence interval = 0.06,0.79) in women who had ever used DMPA (but who had not first used DMPA in the year prior to diagnosis). All 3 exposed cases had also received estrogens pre‐menopausally. Exposure to such estrogens enhanced risk of endometrial cancer and reduced the apparent protective effect of DMPA. Although based on small numbers of exposed women, the protective effect of DMPA appeared to last for at least 8 years after cessation of use. The reduction in risk of endometrial cancer is at least as great for DMPA as for combined oral contraceptives.
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U2 - 10.1002/ijc.2910490207
DO - 10.1002/ijc.2910490207
M3 - Article
C2 - 1831802
AN - SCOPUS:0025826644
SN - 0020-7136
VL - 49
SP - 186
EP - 190
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 2
ER -