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Clinical Pharmacology
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The estrogen alone substudy was also stopped early because an increased risk of stroke was observed, and it was deemed that no further information would be obtained regarding the risks and benefits of estrogen alone in predetermined primary endpoints. Results of the estrogen alone substudy, which included 10,739 women (average age of 63 years, range 50 to 79; 75.3 percent White, 15.1 percent Black, 6.1 percent Hispanic, 3.6 percent Other) after an average follow-up of 6.8 years, are presented in Table 9.
TABLE 9. RELATIVE AND ABSOLUTE RISK SEEN IN THE ESTROGEN
ALONE ONE SUBSTUDY OF WHI
| Event | Relative Risk CE vs Placebo (95% nCIa) |
Placebo n = 5,310 |
CE n = 5,429 |
| Absolute Risk per 10,000 Women-Years |
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| CHD eventsb | 0.95 (0.79–1.16) | 56 | 53 |
| Non-fatal MIb | 0.91 (0.73–1.14) | 43 | 40 |
| CHD deathb | 1.01 (0.71–1.43) | 16 | 16 |
| Strokeb | 1.37 (1.09–1.73) | 33 | 45 |
| Ischemicb | 1.55 (1.19-2.01) | 25 | 38 |
| Deep vein thrombosisb,d | 1.47 (1.06–2.06) | 15 | 23 |
| Pulmonary embolismb | 1.37 (0.90–2.07) | 10 | 14 |
| Invasive breast cancerb | 0.80 (0.62–1.04) | 34 | 28 |
| Colorectal cancerc | 1.08 (0.75–1.55) | 16 | 17 |
| Hip fracturec | 0.61 (0.41–0.91) | 17 | 11 |
| Vertebral fracturesc,d | 0.62 (0.42–0.93) | 17 | 11 |
| Total fracturesc,d | 0.70 (0.63–0.79) | 195 | 139 |
| Death due to other causesc,e | 1.08 (0.88–1.32) | 50 | 53 |
| Overall mortalityc,d | 1.04 (0.88–1.22) | 78 | 81 |
| Global Indexc,f | 1.01 (0.91–1.12) | 190 | 192 |
| aNominal confidence intervals unadjusted for multiple
looks and multiple comparisons. bResults are based on centrally adjudicated data for an average follow-up of 7.1 years. cResults are based on an average follow-up of 6.8 years. dNot included in Global Index. eAll deaths, except from breast or colorectal cancer, definite/probable CHD, PE orcerebrovascular disease. fA subset of the events was combined in a “global index,” defined as the earliest occurrence ofCHD events, invasive breast cancer, stroke, pulmonary embolism, colorectal cancer, hip fracture,or death due to other causes. |
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For those outcomes included in the WHI “global index” that reached statistical significance, the absolute excess risk per 10,000 women-years in the group treated with CE alone were 12 more strokes while the absolute risk reduction per 10,000 women-years was 6 fewer hip fractures. The absolute excess risk of events included in the “global index” was a nonsignificant 2 events per 10,000 women-years. There was no difference between the groups in terms of all-cause mortality. (See BOXED WARNINGS, WARNINGS, and PRECAUTIONS.)
Final centrally adjudicated results for CHD events and centrally adjudicated results for invasive breast cancer incidence from the estrogen alone substudy, after an average follow-up of 7.1 years, reported no overall difference for primary CHD events (nonfatal MI, silent MI and CHD death) and invasive breast cancer incidence in women receiving CE alone compared with placebo (see Table 9).
Centrally adjudicated results for stroke events from the estrogen alone substudy, after an average follow-up of 7.1 years, reported no significant difference in distribution of stroke subtype or severity, including fatal strokes, in women receiving CE alone compared to placebo. Estrogen alone increased the risk of ischemic stroke, and this excess was present in all subgroups of women examined (see Table 9).
Women's Health Initiative Memory Study
The estrogen plus progestin Women's Health Initiative Memory Study (WHIMS), a substudy of WHI, enrolled 4,532 predominantly healthy postmenopausal women 65 years of age and older (47 percent, age 65 to 69 years; 35 percent, 70 to 74 years; 18 percent, 75 years of age and older) to evaluate the effects of daily CE/MPA 0.625 mg conjugated estrogens/2.5 mg medroxyprogesterone acetate on the incidence of probable dementia (primary outcome) compared with placebo.
After an average follow-up of 4 years, 40 women in the estrogen plus progestin group (45 per 10,000 women-years) and 21 in the placebo group (22 per 10,000 women-years) were diagnosed with probable dementia. The relative risk of probable dementia in the hormone therapy group was 2.05 (95 percent CI 1.21–3.48) compared to placebo. It is unknown whether these findings apply to younger postmenopausal women. (See BOXED WARNINGS, WARNINGS, Dementia and PRECAUTIONS, Geriatric Use.)
The estrogen alone WHIMS substudy enrolled 2,947 predominantly healthy postmenopausal women 65 years of age and older (45 percent, age 65 to 69 years; 36 percent, 70 to 74 years; 19 percent, 75 years of age and older) to evaluate the effects of daily CE 0.625 mg on the incidence of probable dementia (primary outcome) compared with placebo.
After an average follow-up of 5.2 years, 28 women in the estrogen alone group (37 per 10,000 women-years) and 19 in the placebo group (25 per 10,000 women-years) were diagnosed with probable dementia. The relative risk of probable dementia in the estrogen alone group was 1.49 (95 percent CI 0.83–2.66) compared to placebo. It is unknown whether these findings apply to younger postmenopausal women. (See BOXED WARNINGS, WARNINGS, Dementia and PRECAUTIONS, Geriatric Use.)
When data from the two populations were pooled as planned in the WHIMS protocol, the reported overall relative risk for probable dementia was 1.76 (95 percent CI 1.19-2.60). Differences between groups became apparent in the first year of treatment. It is unknown whether these findings apply to younger postmenopausal women. (See BOXED WARNINGS, WARNINGS, Dementia and PRECAUTIONS, Geriatric Use.)
Generic Name: Conjugated Estrogens, Medroxyprogesterone Acetate
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