400 likes | 524 Views
Postmenopausal Hormone Therapy And The Risk of Breast Cancer A Contrary Thought. Leon Speroff, M.D. The Cover of The Lancet July 9-15, 2005. “If everything has to be double-blinded, randomised, and evidence-based, where does that leave new ideas?”. Speroff.
E N D
Postmenopausal Hormone Therapy And The Risk of Breast Cancer A Contrary Thought Leon Speroff, M.D.
The Cover of The LancetJuly 9-15, 2005 “If everything has to be double-blinded, randomised, and evidence-based, where does that leave new ideas?” Speroff
Most Important Unanswered Question Postmenopausal Hormone Therapy and the Risk of Breast Cancer: Do hormones initiate new tumor growth or promote the growth of pre-existing tumors? Speroff
WHI: E/P Updated Breast Cancer Report E/P Placebo Ratio Invasive breast ca Year 1 12 19 cases 0.62 (0.29-1.23) Year 2 26 32 0.77 (0.46-1.30) Year 3 29 22 1.26 (0.73-2.20) Year 4 44 27 1.54 (0.95-2.49) Year 5 43 21 1.99 (1.18-3.35) Year 6 + 45 29 1.35 (0.85-2.16) Noninvasive 47 37 (NS) Deaths 4 4 JAMA 2003;289:3243 Speroff
Reanalysis of World’s Breast Cancer Data >>>>>>>>>>>>>>>>>>>>>>>>>>>>> Findings: Current users 5+ years: RR = 1.35 (1.21-1.49) No effect of family history Lancet 350:1047, 1997 Speroff
Reanalysis of World’s Breast Cancer Data Lancet 350:1047, 1997 Current and recent users had no metastatic disease. Decreased risk of fatal breast cancer in users. Speroff
AN APPARENT PARADOX The observational studies that find: Increased risk At the same time, indicate: Decreased mortality Speroff
BETTER PROGNOSIS FOR ESTROGEN USERS Detection/surveillance Bias: Hormone users have more mammograms. Different biology, corrected for mammography: Fewer large tumors, More grade 1 tumors. Bonnier, et al, Obstet Gynecol 85:11, 1995 Manjer, et al, Int J Cancer 92:919, 2001 Gertig, et al, Br Ca Res Treat 80:267, 2003 Pappo, et al, Ann Surg Oncol 11:52, 2004 Speroff
An Answer to the Apparent Paradox Detection/surveillance bias = Earlier diagnosis PLUS Hormonal effects on a pre-existing tumor = Less aggressive stage Speroff
Review of Oregon Experience Long-term hormone users had: More tumors detected by mammography More ductal ca-in-situ More stage I, node negative tumors Better survival rates (100% after 12 yrs) in tumors detected by mammography) No differences in histology or ER status Am J Surg 2008;196:505
The Hormonal EffectOn Pre-Existing Tumors Differentiation of tumor cells (or inhibition of de-differentiation) allowing time for the stromal reaction that leads to earlier detection. Speroff
Causation or Early Detection • Similar results with: hormone therapy, oral contraceptives, and pregnancy. • Observations that favor early detection: • Increase observed very fast. • ER+ lower grade and stage disease. • Return to baseline after therapy. • Better survival rates. Speroff
Ontogeny of Breast Cancer Cancer Starts Here Stem Cells Hormone Effects Ductal Cells Lobular Cells Transition
WHI: Updated Breast Cancer Report E/P Placebo Ratio Invasive breast ca Year 1 12 19 cases 0.62 (0.29-1.23) Year 2 26 32 0.77 (0.46-1.30) Year 3 29 22 1.26 (0.73-2.20) Year 4 44 27 1.54 (0.95-2.49) Year 5 43 21 1.99 (1.18-3.35) Year 6 + 45 29 1.35 (0.85-2.16) Noninvasive 47 37 (NS) After adjustments 1.20 (0.94-1.53) !! JAMA 2003;289:3243 2010;304:1684 Speroff
WHI: Updated Breast Cancer Report Problem with tumor size and localized disease: Tumor size of 1.5-1.8 25-28% positive nodes in literature and SEER 15.8% in WHI placebo group WHI: No nodes examined-9.9/9.1%; missing info-4.0/4.7% Tumors less than 1 cm with no node information were classified as localized disease!! Speroff
0.8 0.6 0.4 0.2 0 E+P PLACEBO DETECTION (%) 0 1 2 3 4 5 6 Maturitas 2006;55:103
OHSU HRT WHI HRT SEER Data, 1983-1987
OHSU No HRT WHI No HRT SEER Data, 1983-1987
WHI: Updated Breast Cancer Report E/P Placebo Ratio Invasive breast ca Year 1 12 19 cases 0.62 (0.29-1.23) Year 2 26 32 0.77 (0.46-1.30) Year 3 29 22 1.26 (0.73-2.20) Year 4 44 27 1.54 (0.95-2.49) Year 5 43 21 1.99 (1.18-3.35) Year 6 + 45 29 1.35 (0.85-2.16) After adjustments 1.20 (0.94-1.53) !! Risk decreased with time!! JAMA 2003;289:3243 2010:304:1684 Maturitas 55:103, 2006 Speroff
WHI Comparison: Trial & Observ. Data “Both yield same conclusions when adjusted for time from menopause to treatment.” Problem: Trial- more BSO, parity differences, less mammography, less prior use, fewer risk factors, older, heavier. THE TWO POPULATIONS DIFFER IN RISK PROFILE!! Am J Epidemiol 2008;167:1207 JNCI 2013;105:526 \ Speroff
WHI: Updated E-Only Breast Cancer Report Overall: HR=0.80; CI=0.62-1.04 Adherent Pts: HR=0.67 CI=0.47-0.97 No effect on in-situ disease. Only ductal cancers and in women with no prior hormone therapy. More follow-up mammograms/biopsies/aspirations. JAMA 2006;295:1647 Speroff
WHI: Differences Between E-P and E Arms • Cardiovascular E-only: more obese, • more hypertension & diabetes, less activity. • Breast Cancer E-only: • – more early and less late births. • – 21% more previous and • 17% more with longer duration • of hormone use. • TWO DIFFERENT POPULATIONS! • Ann Epidemiol 2003;13:S78 Speroff
French E3N Cohort Study SPEROFF 133,744 women; 8.6 years follow-up 55% gels; 45% patches E alone RR = 1.29 (1.02-1.65) E/Progesterone RR = 1.00 (0.83-1.22) E/Progestins RR = 1.77 (1.40-2.24) Int J Cancer 2005;114:448 Breast Cancer Res Treat 2008;107:103 Int J Cancer 2011;128:144
French E3N Cohort Study SPEROFF Nonoral E/Progestins <2yrs: 1.37 (1.07-1.72) <1yr: 1.7 (1.3-2.3) Problems: Users & nonusers not comparable Very fast detection! ? Bioequivalent doses ? E/Progestins: More potent differentiation Int J Cancer 2005;114:448 Breast Cancer Res Treat 2008:107:103
Nurses Health Study: Risk of Invasive Breast Cancer ER+/PR+ <5 yrs 5+ yrs E alone 46 1.02 (0.77-1.38 73 1.37 (1.06-1.78) E/P 112 1.74 (1.40-2.17) 99 2.05 (1.64-2.57) E/P users: younger, lower stage & grade, increase only in ER+/PR+ & greater in lean women. Cancer 101:1490, 2004 Speroff
Is E/P Better? Very large prospective study, 374,465 screened women in 6 U.S. mammography registries: <5 yrs 5+ yrs E alone 0.86 (0.71-1.03) 0.92 (0.84-1.00) E/P 0.85 (0.73-0.98) 1.49 (1.36-1.63) After E/P for 5+ yrs: lower grade & stage, more ER+ J Clin Oncol 21:431, 2003 Speroff
Kaiser Cohort Study 1,081 E only; 1,399 E-P; 4,956 nonusers: Breast Ca Case All Causes Mortality Stage I: E only 1.04 (0.77-1.42) 1.23 (0.72-2.10) E-P 0.69 (0.48-0.99) 0.52 (0.26-1.04) Stage II: E only 0.86 (0.65-1.14) 1.01 (0.72-1.41) E-P 0.53 (0.39-0.73)0.69 (0.48-0.98) Br J Cancer 93:392, 2005 Speroff
Breast Cancer Mortality Cancer Epidem Biomark Prev 17:864, 2008 Collaborative Breast Cancer Study Cohort: 12,269 women in Wisc., Mass., NH; followed 1980 to 2006 Tx at DxAdj. Rate Ratio Former E 0.86 (0.71-1.05) Current E 0.91 (0.77-1.09) Former E-P 0.96 (0.62-1.50) Currrent E-P 0.69 (0.55-0.88) E-P for 5 or more years 0.60 (0.43-0.84)
U.S. Breast Cancer Prevalence NEJM 356:1670, 2007 Rate decreased 2.5% in 2002, 7% in 2003, level in 2004. Mostly ER+ tumors in women ages 50-69, BUT SAME DECREASE IN WOMEN 70+ (low use of hormones). Two possible reasons: 1. Use of mammography declined 2000 through 2005. 2. This decrease occurred within two years of initial WHI reports: WILL PRE-EXISTING TUMORS REGRESS OR SHOW UP LATER? 1.56 Speroff
Geneva Prevalence Statistics BMC Cancer 2006;6:78 Beginning in 1997, peak of breast cancer in Geneva: Increased in younger women, peak at age 60-64. Increase only in Stage I & II disease, ER+ tumors. Increase only in hormone users. 1.56 Speroff
E-P Favorably Influences Gene Expression BMC Medicine 2006;4:16 In ER positive tumors, E-P therapy was associated with better survival, altering the regulation of 276 genes involved in DNA repair and cell-cycle regulation. 1.56 Speroff
Progestins & PR-A, PR-B Molec Endocr 19:574, 2005 Br Ca Res Treat 79:233, 2003 • Genes up-reg. by E are down-reg. by progestins. • PR-A excess: aggressive, poorly diff. tumors. • 4. PR-A dominant in absence of progestins. • 4. Progestins decrease breast tissue levels of PR-A, • producing benefical change in PR-A:PR-B ratio. 1.56 Speroff
Benefits of Progesterone Receptor Molec Endocrinol 2008;22:1812 1. PR functions with and without ligand. 2. Antagonizes inflammatory response. 3. Blocks expression of oncogenic growth factors. 4. Inhibits induction of aromatase enzyme activity. 5. Decreases expression of COX-2, mediator of aromatase and HER-2/neu. 1.56 Speroff
Evidence for Beneficial Effect of Progestins 1. E/P increases receptor-postiive tumors quickly. 2. E/P down regulates estrogen-regulated genes. 3. E/P actives repair and normal function genes. 4. E/P alters the PR-A:PR-B ratio. 5. E/P associated with lower grade/stage tumors and reduces breast cancer mortality. 1.56 Speroff
The Message for Clinicians Effect greater with E/P, more rapid, and lower grade/stage, better survival rates: JAMA 289:3243, 2003 JAMA 289:3254, 2003 Cancer 97:1387, 2003 Cancer 100:2328, 2004 Cancer Causes Control 17:695, 2006 Speroff
The Message for Clinicians Effect in ER+/PR+, lobular cancers, only in current users: JAMA 289:3254, 2003 Br J Cancer 91:644, 2004 Cancer 100:2328, 2004 Cancer 101:1490, 2004 Cancer Causes Control 17:695, 2006 Arch Intern Med 166:1027, 2006 Speroff
The Message for Clinicians There is either a small increase in the risk of breast cancer with E/P or the data reflect an impact on pre-existing tumors. It’s possible that E/P causes greater differentiation and earlier detection of pre- existing tumors resulting in better outcomes. Speroff
The Message for Patients The Risk of Breast Cancer: The evidence does not support a major increase in risk. Positive family history not a contraindication. Speroff
The Message for Patients The Risk of Breast Cancer: 1. A contrasting example. 2. An alternative explanation. Speroff