The table below summarizes the available evidence on the risks and benefits of hormone therapy.
Included are all randomized trials and meta-analyses looking at disease incidence or mortality. Inclusion of observational trials was dependent
on size: case-control studies with 500 or more cases of the disease and cohort studies with at least
2,000 women are included here.
The year noted is when the study results were published. The name following the title of the study is the last
name of the first author on the publication.
|
Year
|
Study
|
Study Type
|
Participants
|
Hormones
|
Results
|
Other Notes
|
|
1984
|
Kaufman
|
Case-control
|
1,610 cases, 1,606 controls
|
E
|
No significant difference in risk
|
|
|
1986
|
Brinton
|
Case-control
|
1,960 cases, 2,258 controls
|
E
|
No difference in risk associated with
ever-use; 20 or more years of use increased risk 50%
|
|
|
1989
|
Adami
|
Cohort
|
23,244
|
E
|
Increases risk 10%
|
Average follow-up 6.7 years
|
|
1989
|
Bergkvist
|
Cohort
|
23,244
|
E, E + P
|
E alone increases risk 70% with 9 years
of use; larger but not significant increase in risk with E + P
|
Average follow-up 5.7 years; majority of
participants used E alone
|
|
1989
|
Mills
|
Cohort
|
20,341
|
E, E + P
|
Current use increases risk 69%
|
No distinction between E and E + P; no
strong increase in risk with increasing duration of use
|
|
1991
|
Kaufman
|
Case-control
|
1,686 cases, 2077 controls
|
E
|
No significant difference in risk
|
|
|
1991
|
Toronto Breast Cancer Study,
Palmer
|
Case-control
|
607 cases, 1,214 controls
|
E, E + P
|
No significant difference in risk
|
93% of participants used E alone
|
|
1992
|
Sillero-Arenas
|
Meta-analysis of 23 studies
|
23 case-control, 13 cohort, 1 randomized
|
E, E + P
|
E alone increases risk by 8%; No increased risk with E + P
|
|
|
1994
|
Risch
|
Cohort
|
32,790
|
E, E + P
|
E alone increases risk 7%/year of use;
no significant difference in risk with E + P
|
|
|
1994
|
Schairer
|
Cohort
|
49,017
|
E, E + P
|
No significant difference in overall
breast cancer risk with either E alone or E + P
|
|
|
1995
|
Nurses' Health Study, Colditz
|
Cohort
|
69,586
|
E, E + P
|
E alone increases risk 32%; E + P
increases risk 41%
|
Average follow-up 10.4 years
|
|
1995
|
La Vecchia
|
Case-control
|
2,569 cases, 2,588 controls
|
E, E + P
|
No change in risk associated with ever-use of either E alone or E + P; increases
risk 100% among former users
who discontinued use within last 10 years; no increase in risk among those
who discontinued use >10 years ago
|
No distinction made between E and E + P for time-dependent analyses
|
|
1995
|
Newcomb
|
Case-control
|
3,130 cases, 3,698 controls
|
E, E + P
|
No significant difference in risk for either E alone or E + P
|
|
|
1995
|
Stanford
|
Case-control
|
537 cases,
492 controls
|
E + P
|
No significant difference in risk
|
|
|
1996
|
Persson
|
Cohort
|
22,597
|
E, E + P
|
E + P increased risk 40% after 10 years follow-up
|
No effect seen with estrogen alone; 13 years of follow-up
|
|
1996
|
Willis
|
Cohort
|
422,373
|
E, E + P
|
Decreases breast cancer mortality 16%
|
9 years of follow-up; No distinction between E vs. E + P
|
|
1997
|
Collaborative Group on Hormonal Factors in Breast Cancer
|
Meta-analysis
|
52,705 cases
108,411controls
|
E, E + P
|
Incidence of breast cancer increases
with increasing duration of hormone use
|
Where data was available for type of hormone use (39% of women), on significant difference in risk between E and E + P; effect nearly disappears 5 years after
stopping
|
|
1997
|
Sellers
|
Cohort
|
41,837
|
E, E
+ P
|
No increased risk among women with
family history of breast cancer
|
No distinction between E vs. E + P
|
|
1997
|
Tavani
|
Case-control
|
5,984 cases, 5,504 controls
|
E, E + P
|
Increased risk 20%
|
No distinction between E vs. E + P
|
|
1998
|
Sourander
|
Cohort
|
7,944
|
E
|
No significant difference in risk
|
8 years of follow-up
|
|
1999
|
Lando
|
Cohort
|
5,761
|
E, E + P
|
No significant difference in risk
|
No distinction between E vs. E + P; 22 years of follow-up
|
|
1999
|
Magnusson
|
Case-control
|
3,345 cases, 3,454 controls
|
E, E + P
|
10 or more years of use E alone increases risk 170%; 10 or more years of use E + P increases risk 195%
|
Similar results for former and current
users
|
|
1999
|
Schairer
|
Cohort
|
2,614
|
E
|
Reduces mortality when continued after
cancer diagnosis
|
Mortality results determined 14-22 years post-diagnosis
|
|
2000
|
Ross
|
Case-control
|
3,534
|
E, E + P
|
Increases risk approximately 10% for
each 5 years of use
|
Greater increase in risk among E + P
users than E alone
|
|
2000
|
Pike
|
Case-control
|
3,794 cases, 3,343 controls
|
E, E + P
|
No increased risk with E alone; E + P
increases risk 24% per 5 years of use
|
|
|
2000
|
Schairer
|
Cohort
|
46,355
|
E, E + P
|
Increases risk 1% to 8% for each year of
use
|
Greater increase in risk among E + P
users than E alone
|
|
2000
|
Nurses' Health Study, Colditz
|
Cohort
|
58,520
|
E, E + P
|
Five or more years of use increases risk
40%
|
Greater increase in risk among E + P
users than E alone; increased risk disappears after 2-5 years
discontinuation of use
|
|
2001
|
O'Meara
|
Cohort
|
2,755
|
E, E + P
|
Hormone reduces recurrence and mortality when continued after cancer
diagnosis
|
79% of hormone users used E alone;
results determined 2-19 years after diagnosis
|
|
2002
|
Women's Health Initiative
|
Randomized
|
16,608
|
E + P
|
Increases risk 26%
|
5.2 years of follow-up
|