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Menopoz
HT
(MHT)
Meme
Kanseri
Prof. Dr. Levent M. ŞENTÜRK
• Breast cancer is the most frequent cancer diagnosis in
women (lifetime risk 10%)
• There was a significant increase in incidence rates for
premenopausal and postmenopausal BC in around 20 of
44 populations over the last decade (1998-2012)
• The increase in premenopausal BC is largely in high
income countries
• 2018 BC incidence (/100,000) in high income countries
Premenopausal: 30.6
Postmenopausal: 256
2020
2020
Breast Cancer Epidemiology
• Fig: Average annual
percentage change for
premenopausal and
postmenopausal breast
cancer, 1998–2012
2020
Trends in premenopausal
and postmenopausal
breast cancer truncated
ASIRs, 1998–2012, for each
country
Premenopausal breast
cancer defined as age <50
years and postmenopausal
breast cancer defined as
age ≥50 years
ASIR: age-standardized
incidence rate
• BC risk is lower in women with
• Late menarche
• Early menopause
• Having children early
• Having more children
• Longer duration of breast feeding
Breast Cancer Epidemiology
Reproductive factors
Evidence on breast cancer and MHT
• RR for MHT (=E+P) > E only
• WHI EPT HR: 1.26 (1.01-1.59)
• WHI ET HR: 0.77 (0.62-0.95)
• Progesterone / dydrogesterone < synthetic P
• Continuous > sequential
• Duration effect
• Promoter effect (RR ceased following discontinuation)
• Increase: lobular > ductal
• Better differentiation
• No increase in mortality
After 20 years, no more increase in the
RR, no more deaths… Chlebowski, et al., 2020
8.2y
After 20 years, no more increase in the
RR, no more deaths… Chlebowski, et al., 2020
• WHI: 26,525 postmenopausal wopmen with a
hysterectomy, 50-79yrs. Follow-up 8.2yrs. 
• WHI: No difference (CEE) low vs. standard dose (0.625 mg)
(HR: 0.99 (0.65-1.48))
• WHI: No difference (route): TD E2 vs CEE 0.625mg
(HR: 0.75 (0.47-1.19))
• E2 + progesterone / dydrogesterone;
Finnish registry: E2 + DYD; <5 yrs
RR=1.00
French case-ctrl study: E2 + P/DYD;
RR=0.80 (0.44-1.43)
Shufelt, et al., 2018
Lyytinen et al., 2016
BC - Difference in E / P
Cordina-Duverget et al., 2013
Shufelt, et al., 2018
BC: The level of risk (by Gail)
High risk (>4.00)
• BRCA mut., Family hx: 1st degree premenopausal
• Bx: atypical hyperplasia, LCIS, DCIS
• High breast density: BI-RADS D
• Thoracic radiation
Intermediate risk (≤2.00)
• Reproductive factors: obesity, young age at menarche, nulliparity
• Family hx at older age, Med. breast density: BI-RADS C
• DM, Obesity (post-menopausal)(x1.20-2.50); Alcohol (x1.05-1.40)
Lower risk (<1.00)
• Breast-feeding (>12 mo); Low breast density: BI-RADS A; B
• Multiparity? (≥5; 1st<25 y/o!), low BMI, low BMD, VMS (?SWAN)
• Exercise, Wt. loss at any age;
• Obesity receiving MHT: No increase
GAIL:
www.cancer.gov/bcrisktool
IBIS tool: www.ems-
trials.org/riskevaluator
Breast Imaging Reporting and Data
System (BI-RADS)
(Breast Density; four levels)
Excess risk according to the
baseline risk (by Gail) (1/1,000w)
Santen et al., 2020
Mastalgia as a risk factor for BC (WHI)
Crandall et al., 2011
Modifiable risk factors for BC
• Alcohol: dose dependent
• Inactivity: Exercise decreases the risk even in
women under MHT
• BMI: Weight loss
MHT and Mortality
Benkhadra et al., 2015
• MHT does not affect the risk of death from all
causes (43 RCTs)
• RCTs including women with
• mean age less than 60 and
• MHT started less than 10 years after menopause
showed a reduction of mortality 
RR: 0.70 (0.52-0.95)
BC risk in premenopausal
LNG-IUS20 users
• Two newer high quality registry-based studies
including women aged 18-40 years (premenopausal)
observing >500,000 wy of use found a minimal but
significant risk increase for current users. RR: 1.27
• In the Finnish study an increase in risk was
significant only for a > 5-years-duration of use
• Absolute numbers
• Non-hormonal contraception 55 cases/100,000 wy
• LNG-IUS 70 cases/100,000 wy
+15 cases/100,000 wy
Morch, et al., 2017; Soini et al., 2016
Soini et al., 2016
BC risk in peri and postmenopausal
LNG-IUS20 users
Breast cancer risk and MHT
SUMMARY
BC risk is lower
• With E alone than with EP combination
• With E in combination with Progestorone / Didrogesterone
(DG) than in combination with other progestins (=synthetic)
Breast cancer risk and MHT
SUMMARY
BC risk is lower
• With E alone than with EP combination
• With E in combination with Progestorone / Didrogesterone
(DG) than in combination with other progestins (=synthetic)
Incidence of BC
• Increases with duration of use (Absolute numbers !!!)
• Decreases with time since last use
• Increases with increasing breast density
• Increases with breast tenderness (mastalgia) in EPT, not ET
• No increase in POF!!! No further increase in obese women
Breast cancer risk and MHT
SUMMARY
BC risk is lower
• With E alone than with EP combination
• With E in combination with Progestorone / Didrogesterone
(DG) than in combination with other progestins (=synthetic)
Incidence of BC
• Increases with duration of use (Absolute numbers !!!)
• Decreases with time since last use
• Increases with increasing breast density
• Increases with breast tenderness (mastalgia) in EPT, not ET
• No increase in POF!!! No further increase in obese women
MHT
• Does not cause BC, but has a promoter effect
• Important to stratify on the level of individual risk
• Reduces mortality from all causes (after menopause)
Menopoz
HT
(MHT)
Meme
Kanseri
Prof. Dr. Levent M. ŞENTÜRK
Menopoz
HT
(MHT)
Meme
Kanseri
Prof. Dr. Levent M. ŞENTÜRK
Menopoz
HT
(MHT)
Meme
Kanseri
Prof. Dr. Levent M. ŞENTÜRK
Breast cancer risk and MHT IMS, Keypoints
• The increased risk is primarily associated with the addition of a
synthetic progestogen to estrogen therapy and to duration of
use [B]
• The risk may be lower with micronized progesterone or
dydrogesterone [C]
• The MHT attributable risk is small and decreases when
treatment stops [B]
• There is a lack of safety data supporting MHT use in breast
cancer survivors
• Breast cancer risk should be evaluated before MHT prescription
[D]*
• Any possible increased risk associated with MHT may be
decreased by selecting women with lower baseline risk
including low breast density and by providing education on
preventive lifestyle measures (reducing weight, reducing
alcohol intake, increasing physical activity) [D]
Meta-analysis (51 studies) 1.35 1
NHS EPT 1.32 2
WHI EPT 1.26 3
WHI EPT 1.24 4
MWS EPT/ET 1.66 5
1 . Lancet 1997;350:1047
2 . Chen WY et al, Ann Intern Med
2002;137:798
3. Writing Group for WHI, JAMA
2002;288:321
Study RR
Hormone therapy is associated with a small but significant
risk of breast cancer
4. Chlebowski et al, JAMA
2003;289:3243
5. Beral V, Lancet 2003;362:419-27
Characteristics of HT regimen and breast cancer risk
A. Characteristics of HT regimen
B. Real impact of risk (attributable risk)
1. Estrogen monotherapy versus combined EPT
2. Duration of use
3. Mode (sequential versus continuous)
4. Route (oral versus transdermal)
5. Dose
6. Type of estrogen
7. Type of progestin
1. Estrogen monotherapy versus combined EPT therapy
• EPIC study:
prospective
observational study
• 10 European
countries
• 134,000 women
• Mean follow-up: 8.6
years
Bakken K et al, Int J Cancer 2010
2. Breast cancer risk increases with duration of HT use
EPIC Study, Bakken K et al, Int J Cancer 2010
WHI Study: women with no prior exposure to HT
had no increased risk of breast cancer
Anderson GL,
Maturitas
2006;55:103
1,2
1,3
1,4
1,5
1,6
1,7
1,8
1,9
2
sequentialHT fixed continuous
RR
3. Continuous regimens may be associated with higher
risk compared to sequential regimens
EPIC Study, Bakken K et al,
Int J Cancer 2010
The cumulative exposure to
progestin is lower with the
sequential regimens
Lyytinen H et al, Int J Cancer 2010
• Finnish case-control study
• 10,000 cases and 30,000 controls
aged 50-62
4. The route of HT does not modify the risk of breast
cancer
Oral HT
Transdermal HT
Lyytinen H et al, Int J Cancer 2010
RR
RR
Cases controls
Cases controls
Bakken K et al, Int J Cancer 2010
EPIC study: oral versus transdermal RR 1.13 (NS)
5. Dose of estrogen in HT and breast cancer risk
• No RCT on the effect of different HT doses on
breast cancer risk
• Lower estrogen doses have less impact on breast
density1
• Breast density is a surrogate marker of breast
cancer
Martin LJ et al, Maturitas 2009;64:20-26
Stuedal A Climacteric 2009;12:248-58
Grady D Menopause 2007;14:391-6
Identical HT regimens differing only in E2 dose are
associated with different increases in breast density
Christodoulakos G, Lambrinoudaki I, Vourtsi A et al, Maturitas 2006;54:78
% of subjects with breast density increase
0
5
10
15
20
25
30
35
CEE/MPA low E2/NETA E2/NETA
p=0.6
p=0.04 p=0.04
6. The type of estrogen in HT does not influence
breast cancer risk
• No RCT directly comparing CEE to E2
• EPIC study:
compound RR of breast cancer
estradiol 1.08 – 1.61
CEE 1.16 – 2.18
RR CEE versus E2: 1.15 NS
Bakken K et al, Int J Cancer 2010
• E3N Study (French component of EPIC)
• 80,391 postmenopausal teachers in France
• Mean follow-up: 8.1 years
Fournier A et al, J Clin Oncol 2008;26:1260
7. The type of progestin may modify breast cancer risk
7. The type of progestin may modify breast cancer risk
• All Finnish women > 50 years (221,551 women)
• Follow – up 1994 – 2005
• 6,211 incident cases of breast cancer
Lyytinen H et al, Obstet Gynecol 2009;113:65
B. HT and absolute risk of breast cancer
• Baseline 5-year absolute risk: 1.1%
• HT related RR: 1.26 (WHI)
5-year risk of breast cancer attributable to
HT: 3 women in 1000
Among 50-year old women who use HT (CEE/MPA)
for 5 years, 14 out of 1000 will develop breast cancer
until the age of 55
Risk factors of breast cancer: comparative assessment
Risk factors
• ΒΜΙ (>29,7 Kg/m2) 1.26-2.52
• alcohol (20g /day x 5 years) 1.28
• Hormone Therapy (EPT / WHI) 1.26
• 1st delivery > 30 years 1.5
• Family history of breast cancer 1.5
• Benign breast disease - breast biopsy 1.6-2.8
• Increased breast density 2.0-4.0
RR
Shah NR, Exp Opin Pharmacotherapy 2006;7(18):2455-63
Pichard C et al, Maturitas 2008;60:19-30
Mammographic patterns according to BI-RADS system
I II III IV
< 25% dense > 75% dense
51-75% dense
25-50% dense
RR 1.0 2.03 2.95 4.03
Cummings SR, J Natl Cancer Institute 2009;101:384-389
Individual breast cancer risk assessment
• Age, age at menarche and menopause
• BMI, adult weight gain
• Family history of breast cancer (1st degree relative)
• Benign breast disease requiring FNA or biopsy
• Previous hormone therapy
• Nulliparity / 1st delivery > 30years
• Daily alcohol intake
• Breast density
Vogel VG et al, Menopause 2008; 15(4 Suppl):782
Santen RJ et al, Endocr Relat Cancer. 2007 Jun;14(2):169-87
Risk factor patient
age 52
menarche 12
1st delivery 27
1st degree relative with breast cancer NO
Breast biopsy NO
Race white
Individual breast cancer risk assessment
US National Institutes of Health, www.cancer.gov accessed April 2010
Patient 5-year risk: 1.2%
Average 5-year risk: 1.4%
National Cancer Institute breast cancer
risk assessment tool
• Breast density:
BI-RADS II
• BMI: 27
• Menopause: 51
Risk factor patient
age 52
menarche 12
1st delivery 34
1st degree relative with breast cancer YES
Breast biopsy YES
No of biopsies 1
Atypical hyperplasia NO
Race white
Individual breast cancer risk assessment
US National Institutes of Health, www.cancer.gov accessed April 2010
Patient 5-year risk: 2.5%
Average 5-year risk: 1.4%
US National Cancer Institute breast
cancer risk assessment tool
• Breast density:
BI-RADS III
• BMI: 27
• Menopause: 51
Summary
• Hormone therapy is associated with a small, but
statistically significant increase in breast cancer risk
• The risk is more apparent with continuous
combined HT regimens
• The risk increases with duration of use
• The risk may differ by the progestin in the HT
regimen
• The absolute risk is small and in most cases has
minor clinical relevance
• HT is acceptable, provided a thorough
assessment of individual risk is performed in each
woman
Lvnt tsmo world menopause day mtg_bionorica_20201214_menopause_mht_meme ca
Lvnt tsmo world menopause day mtg_bionorica_20201214_menopause_mht_meme ca

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Lvnt tsmo world menopause day mtg_bionorica_20201214_menopause_mht_meme ca

  • 2. • Breast cancer is the most frequent cancer diagnosis in women (lifetime risk 10%) • There was a significant increase in incidence rates for premenopausal and postmenopausal BC in around 20 of 44 populations over the last decade (1998-2012) • The increase in premenopausal BC is largely in high income countries • 2018 BC incidence (/100,000) in high income countries Premenopausal: 30.6 Postmenopausal: 256 2020
  • 4. Breast Cancer Epidemiology • Fig: Average annual percentage change for premenopausal and postmenopausal breast cancer, 1998–2012
  • 5. 2020 Trends in premenopausal and postmenopausal breast cancer truncated ASIRs, 1998–2012, for each country Premenopausal breast cancer defined as age <50 years and postmenopausal breast cancer defined as age ≥50 years ASIR: age-standardized incidence rate
  • 6. • BC risk is lower in women with • Late menarche • Early menopause • Having children early • Having more children • Longer duration of breast feeding Breast Cancer Epidemiology Reproductive factors
  • 7. Evidence on breast cancer and MHT • RR for MHT (=E+P) > E only • WHI EPT HR: 1.26 (1.01-1.59) • WHI ET HR: 0.77 (0.62-0.95) • Progesterone / dydrogesterone < synthetic P • Continuous > sequential • Duration effect • Promoter effect (RR ceased following discontinuation) • Increase: lobular > ductal • Better differentiation • No increase in mortality
  • 8. After 20 years, no more increase in the RR, no more deaths… Chlebowski, et al., 2020 8.2y
  • 9. After 20 years, no more increase in the RR, no more deaths… Chlebowski, et al., 2020
  • 10. • WHI: 26,525 postmenopausal wopmen with a hysterectomy, 50-79yrs. Follow-up 8.2yrs.  • WHI: No difference (CEE) low vs. standard dose (0.625 mg) (HR: 0.99 (0.65-1.48)) • WHI: No difference (route): TD E2 vs CEE 0.625mg (HR: 0.75 (0.47-1.19)) • E2 + progesterone / dydrogesterone; Finnish registry: E2 + DYD; <5 yrs RR=1.00 French case-ctrl study: E2 + P/DYD; RR=0.80 (0.44-1.43) Shufelt, et al., 2018 Lyytinen et al., 2016 BC - Difference in E / P Cordina-Duverget et al., 2013 Shufelt, et al., 2018
  • 11. BC: The level of risk (by Gail) High risk (>4.00) • BRCA mut., Family hx: 1st degree premenopausal • Bx: atypical hyperplasia, LCIS, DCIS • High breast density: BI-RADS D • Thoracic radiation Intermediate risk (≤2.00) • Reproductive factors: obesity, young age at menarche, nulliparity • Family hx at older age, Med. breast density: BI-RADS C • DM, Obesity (post-menopausal)(x1.20-2.50); Alcohol (x1.05-1.40) Lower risk (<1.00) • Breast-feeding (>12 mo); Low breast density: BI-RADS A; B • Multiparity? (≥5; 1st<25 y/o!), low BMI, low BMD, VMS (?SWAN) • Exercise, Wt. loss at any age; • Obesity receiving MHT: No increase GAIL: www.cancer.gov/bcrisktool IBIS tool: www.ems- trials.org/riskevaluator
  • 12. Breast Imaging Reporting and Data System (BI-RADS) (Breast Density; four levels)
  • 13. Excess risk according to the baseline risk (by Gail) (1/1,000w) Santen et al., 2020
  • 14. Mastalgia as a risk factor for BC (WHI) Crandall et al., 2011
  • 15. Modifiable risk factors for BC • Alcohol: dose dependent • Inactivity: Exercise decreases the risk even in women under MHT • BMI: Weight loss
  • 16. MHT and Mortality Benkhadra et al., 2015 • MHT does not affect the risk of death from all causes (43 RCTs) • RCTs including women with • mean age less than 60 and • MHT started less than 10 years after menopause showed a reduction of mortality  RR: 0.70 (0.52-0.95)
  • 17. BC risk in premenopausal LNG-IUS20 users • Two newer high quality registry-based studies including women aged 18-40 years (premenopausal) observing >500,000 wy of use found a minimal but significant risk increase for current users. RR: 1.27 • In the Finnish study an increase in risk was significant only for a > 5-years-duration of use • Absolute numbers • Non-hormonal contraception 55 cases/100,000 wy • LNG-IUS 70 cases/100,000 wy +15 cases/100,000 wy Morch, et al., 2017; Soini et al., 2016 Soini et al., 2016
  • 18. BC risk in peri and postmenopausal LNG-IUS20 users
  • 19. Breast cancer risk and MHT SUMMARY BC risk is lower • With E alone than with EP combination • With E in combination with Progestorone / Didrogesterone (DG) than in combination with other progestins (=synthetic)
  • 20. Breast cancer risk and MHT SUMMARY BC risk is lower • With E alone than with EP combination • With E in combination with Progestorone / Didrogesterone (DG) than in combination with other progestins (=synthetic) Incidence of BC • Increases with duration of use (Absolute numbers !!!) • Decreases with time since last use • Increases with increasing breast density • Increases with breast tenderness (mastalgia) in EPT, not ET • No increase in POF!!! No further increase in obese women
  • 21. Breast cancer risk and MHT SUMMARY BC risk is lower • With E alone than with EP combination • With E in combination with Progestorone / Didrogesterone (DG) than in combination with other progestins (=synthetic) Incidence of BC • Increases with duration of use (Absolute numbers !!!) • Decreases with time since last use • Increases with increasing breast density • Increases with breast tenderness (mastalgia) in EPT, not ET • No increase in POF!!! No further increase in obese women MHT • Does not cause BC, but has a promoter effect • Important to stratify on the level of individual risk • Reduces mortality from all causes (after menopause)
  • 25. Breast cancer risk and MHT IMS, Keypoints • The increased risk is primarily associated with the addition of a synthetic progestogen to estrogen therapy and to duration of use [B] • The risk may be lower with micronized progesterone or dydrogesterone [C] • The MHT attributable risk is small and decreases when treatment stops [B] • There is a lack of safety data supporting MHT use in breast cancer survivors • Breast cancer risk should be evaluated before MHT prescription [D]* • Any possible increased risk associated with MHT may be decreased by selecting women with lower baseline risk including low breast density and by providing education on preventive lifestyle measures (reducing weight, reducing alcohol intake, increasing physical activity) [D] Meta-analysis (51 studies) 1.35 1 NHS EPT 1.32 2 WHI EPT 1.26 3 WHI EPT 1.24 4 MWS EPT/ET 1.66 5 1 . Lancet 1997;350:1047 2 . Chen WY et al, Ann Intern Med 2002;137:798 3. Writing Group for WHI, JAMA 2002;288:321 Study RR Hormone therapy is associated with a small but significant risk of breast cancer 4. Chlebowski et al, JAMA 2003;289:3243 5. Beral V, Lancet 2003;362:419-27
  • 26. Characteristics of HT regimen and breast cancer risk A. Characteristics of HT regimen B. Real impact of risk (attributable risk) 1. Estrogen monotherapy versus combined EPT 2. Duration of use 3. Mode (sequential versus continuous) 4. Route (oral versus transdermal) 5. Dose 6. Type of estrogen 7. Type of progestin
  • 27. 1. Estrogen monotherapy versus combined EPT therapy • EPIC study: prospective observational study • 10 European countries • 134,000 women • Mean follow-up: 8.6 years Bakken K et al, Int J Cancer 2010
  • 28. 2. Breast cancer risk increases with duration of HT use EPIC Study, Bakken K et al, Int J Cancer 2010
  • 29. WHI Study: women with no prior exposure to HT had no increased risk of breast cancer Anderson GL, Maturitas 2006;55:103
  • 30. 1,2 1,3 1,4 1,5 1,6 1,7 1,8 1,9 2 sequentialHT fixed continuous RR 3. Continuous regimens may be associated with higher risk compared to sequential regimens EPIC Study, Bakken K et al, Int J Cancer 2010 The cumulative exposure to progestin is lower with the sequential regimens Lyytinen H et al, Int J Cancer 2010 • Finnish case-control study • 10,000 cases and 30,000 controls aged 50-62
  • 31. 4. The route of HT does not modify the risk of breast cancer Oral HT Transdermal HT Lyytinen H et al, Int J Cancer 2010 RR RR Cases controls Cases controls Bakken K et al, Int J Cancer 2010 EPIC study: oral versus transdermal RR 1.13 (NS)
  • 32. 5. Dose of estrogen in HT and breast cancer risk • No RCT on the effect of different HT doses on breast cancer risk • Lower estrogen doses have less impact on breast density1 • Breast density is a surrogate marker of breast cancer Martin LJ et al, Maturitas 2009;64:20-26 Stuedal A Climacteric 2009;12:248-58 Grady D Menopause 2007;14:391-6
  • 33. Identical HT regimens differing only in E2 dose are associated with different increases in breast density Christodoulakos G, Lambrinoudaki I, Vourtsi A et al, Maturitas 2006;54:78 % of subjects with breast density increase 0 5 10 15 20 25 30 35 CEE/MPA low E2/NETA E2/NETA p=0.6 p=0.04 p=0.04
  • 34. 6. The type of estrogen in HT does not influence breast cancer risk • No RCT directly comparing CEE to E2 • EPIC study: compound RR of breast cancer estradiol 1.08 – 1.61 CEE 1.16 – 2.18 RR CEE versus E2: 1.15 NS Bakken K et al, Int J Cancer 2010
  • 35. • E3N Study (French component of EPIC) • 80,391 postmenopausal teachers in France • Mean follow-up: 8.1 years Fournier A et al, J Clin Oncol 2008;26:1260 7. The type of progestin may modify breast cancer risk
  • 36. 7. The type of progestin may modify breast cancer risk • All Finnish women > 50 years (221,551 women) • Follow – up 1994 – 2005 • 6,211 incident cases of breast cancer Lyytinen H et al, Obstet Gynecol 2009;113:65
  • 37. B. HT and absolute risk of breast cancer • Baseline 5-year absolute risk: 1.1% • HT related RR: 1.26 (WHI) 5-year risk of breast cancer attributable to HT: 3 women in 1000 Among 50-year old women who use HT (CEE/MPA) for 5 years, 14 out of 1000 will develop breast cancer until the age of 55
  • 38. Risk factors of breast cancer: comparative assessment Risk factors • ΒΜΙ (>29,7 Kg/m2) 1.26-2.52 • alcohol (20g /day x 5 years) 1.28 • Hormone Therapy (EPT / WHI) 1.26 • 1st delivery > 30 years 1.5 • Family history of breast cancer 1.5 • Benign breast disease - breast biopsy 1.6-2.8 • Increased breast density 2.0-4.0 RR Shah NR, Exp Opin Pharmacotherapy 2006;7(18):2455-63 Pichard C et al, Maturitas 2008;60:19-30
  • 39. Mammographic patterns according to BI-RADS system I II III IV < 25% dense > 75% dense 51-75% dense 25-50% dense RR 1.0 2.03 2.95 4.03 Cummings SR, J Natl Cancer Institute 2009;101:384-389
  • 40. Individual breast cancer risk assessment • Age, age at menarche and menopause • BMI, adult weight gain • Family history of breast cancer (1st degree relative) • Benign breast disease requiring FNA or biopsy • Previous hormone therapy • Nulliparity / 1st delivery > 30years • Daily alcohol intake • Breast density Vogel VG et al, Menopause 2008; 15(4 Suppl):782 Santen RJ et al, Endocr Relat Cancer. 2007 Jun;14(2):169-87
  • 41. Risk factor patient age 52 menarche 12 1st delivery 27 1st degree relative with breast cancer NO Breast biopsy NO Race white Individual breast cancer risk assessment US National Institutes of Health, www.cancer.gov accessed April 2010 Patient 5-year risk: 1.2% Average 5-year risk: 1.4% National Cancer Institute breast cancer risk assessment tool • Breast density: BI-RADS II • BMI: 27 • Menopause: 51
  • 42. Risk factor patient age 52 menarche 12 1st delivery 34 1st degree relative with breast cancer YES Breast biopsy YES No of biopsies 1 Atypical hyperplasia NO Race white Individual breast cancer risk assessment US National Institutes of Health, www.cancer.gov accessed April 2010 Patient 5-year risk: 2.5% Average 5-year risk: 1.4% US National Cancer Institute breast cancer risk assessment tool • Breast density: BI-RADS III • BMI: 27 • Menopause: 51
  • 43. Summary • Hormone therapy is associated with a small, but statistically significant increase in breast cancer risk • The risk is more apparent with continuous combined HT regimens • The risk increases with duration of use • The risk may differ by the progestin in the HT regimen • The absolute risk is small and in most cases has minor clinical relevance • HT is acceptable, provided a thorough assessment of individual risk is performed in each woman