Also this:
BMJ. 2012 Oct 9;345
"The women in the treated group with an intact uterus started treatment with 2 mg synthetic 17-β-estradiol for 12 days, 2 mg 17-β-estradiol plus 1 mg norethisterone acetate for 10 days, and 1 mg 17-β-estradiol for six days (Trisekvens; Novo Nordisk, Denmark). In women who had undergone hysterectomy, first line treatment was 2 mg 17-β-estradiol a day (Estrofem; Novo Nordisk, Denmark)."
(during intervention, after 10 yrs)
"The occurrence of any cancer did not differ significantly (39 in control group v 36 in treated group; 0.92, 0.58 to 1.45; P=0.71) or breast cancer (17 in control group v 10 in treated group, 0.58, 0.27 to 1.27; P=0.17; fig 4). The occurrence of other cancers did not differ significantly (25 in control group v 26 in treated group; 1.04, 0.60 to 1.80; P=0.88): three women in the control group had a diagnosis of both breast cancer and other cancer. The composite endpoint mortality or breast cancer applied to 40 women in the control group and 22 in the treated group (0.54, 0.32 to 0.91, P=0.020)."
(6 yrs after intervention, follow-up)
"The groups did not differ significantly for breast cancer (26 in control group v 24 in treated group; 0.90, 0.52 to 1.57; P=0.72) or for other cancers (43 in control group v 52 in treated group; 1.21, 0.81 to 1.82; P=0.35, fig 6)."
"A significant interaction was found between hormone replacement therapy and age at baseline for the composite endpoint mortality or breast cancer (P=0.028) with the younger women (<50 years) receiving hormone therapy having a significantly reduced risk (0.49, 0.28 to 0.87, P=0.015, fig 6). Women who had undergone hysterectomy (n=192) and received oestrogen alone had a decreased risk of death or breast cancer compared with women in the control group (0.42, 0.18 to 0.97; P=0.043; fig 6)."
"The rate of breast cancer and other cancer was not increased in the present study, but because of the potential time lag a longer follow-up may be necessary to make more definite conclusions."