Overview
Women at risk for development of breast cancer and experiencing vasomotor menopausal symptoms (hot flashes) will be randomized to bazedoxifene (BZA) plus conjugated estrogens (CE) for 6 months versus a wait list control. Two risk factors for development of breast cancer will be studied pre-study and after 6 months: fibroglandular volume (FGV) on mammogram as assessed by Volpara software and proliferation by Ki-67 immunocytochemistry in benign breast tissue acquired by random periareolar fine needle aspiration (RPFNA). Change in biomarkers will be compared between groups.
Description
Phase IIB trial of 6 months of BZA 20 mg +CE 0.45 mg (subsequently designated as BZA+CE) vs a waitlist control. Trial is informed by prior results of a single arm trial that used Duavee® (combination of BZA+CE that is FDA-approved for relief of hot flashes). Since Duavee® is currently not available commercially, the two separate components are used instead. Breast imaging, benign breast tissue by RPFNA, and blood for biomarkers will be obtained at baseline and at 6 months using similar assessment techniques. The primary endpoint is the difference between the BZA+CE and control groups for absolute change from baseline to 6 months in the risk biomarker fibroglandular volume (FGV). Volpara® fully automated assessments overcome the interpretive variance inherent in subjective assessments. Additional endpoints include changes in benign breast epithelial immunolabeling for Ki-67, estrogen receptor alpha (ERα), progesterone receptor (PR), and anterior gradient-2 protein (AGR2); and systemic levels of bioavailable hormones, IGF-1, IGFBP3, and measures of insulin sensitivity. The modifying effects of baseline BMI, visceral adipose, and plasma BZA concentrations on markers will be studied.
Eligibility
Inclusion Criteria for Baseline Mammogram and RPFNA Women ages 45 - 60 or ages 61-64 if
their last mammogram was described as heterogeneously or extremely dense.
Current vasomotor symptoms (hot-flashes, night sweats or both). These do not need to be
frequent or severe but should occur at least once a week. Women who feel that they would
likely need a supplement or be at high risk of withdrawal if they were randomized to
waitlist because of vasomotor symptoms are not good candidates for this trial.
Women must be in one of the four menopausal status categories, as defined below.
- Age 45-64 with an intact uterus and no periods in past 12 months. Amenorrhea is not
thought to be due to endometrial ablation, Mirena IUD or other menses suppressing
contraceptives. Category 1: Clinically Postmenopausal
- Age 45-64 with an intact uterus and no periods in past 2 months immediately preceding
eligibility testing; but has not been amenorrheic for 12 months. Amenorrhea not
thought to be due to endometrial ablation, Mirena IUD or other menses suppressing
contraceptives. Category 2: Late menopause transition.
- Age 50-64 and prior hysterectomy, prior endometrial ablation with subsequent lack of
periods, or menses suppression due to Mirena IUD or other types of contraceptives.
Category 3: Menopause transition by symptoms; uterus not intact or menses suppression;
age ≥50.
- Age 45-49 and prior hysterectomy, prior endometrial ablation with subsequent lack of
periods, or menses suppression due to Mirena IUD or other types of contraceptives.
Category 4: Menopause transition by symptoms uterus not intact or menses suppression;
age 45-49.
Must have at least one ovary.
BMI: ≤ 38 kg/m2
At least one breast without prior therapeutic radiation that can be assessed by Volpara®
software.
Chemistry profile showing reasonably normal renal and hepatic function: creatinine <2.0
mg/dL, bilirubin < 2.5 mg/dL, and albumin > 3.4 g/dL within the past 12 months.
Risk Factors/Level. Moderate risk of developing breast cancer based on having at least one
of following:
- First or second degree relative with breast cancer age 60 or younger;
- A prior breast biopsy showing proliferative breast disease, including hyperplasia,
atypical hyperplasia, or lobular carcinoma in situ
- 2 or more prior biopsies regardless of benign histology
- Prior ER-PR- or low risk ER+ DCIS at minimum treated with surgical removal of lesion
with or without radiation therapy.
- Surgical removal of DCIS is defined as no DCIS cells within 2 mm of the margin or if
DCIS cells were present at the margin, a subsequent resection shows no DCIS cells and
there were no residual calcifications on the mammogram.
- Low risk ER+ and/or PR+ DCIS is defined as that which is ≤2 cm in diameter, non-high
grade and occurring in women who are 50 or older.
- Women with known gene mutations associated with an increased risk for breast cancer
such as ATM, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, STK11, P53, PTEN (Note: BRCA1/2 are
excluded as women 45 and over should have undergone risk-reducing bilateral
salpingo-oophorectomy).
- 10-year relative risk of ≥2X that for the average population for age group as
calculated by IBIS Breast Cancer Risk Evaluation Tool version 8 (Tyrer-Cuzick)
(http://www.ems-trials.org/riskevaluator/); or 10 year risk based on the Breast Cancer
Surveillance Consortium tool Version 2
(https://tools.bcsc-scc.org/BC5yearRisk/calculator.htm)
Vaginal Hormones: Low dose vaginal hormones, such as Estring(®, Vagifem®, Imvexy®, or 0.5
gram or less of conjugated estrogen vaginal cream twice weekly or less often, for vaginal
dryness and dyspareunia may be continued at the same dose.
Systemic Hormones: If previously on oral contraceptives or systemic hormone replacement
such as pills, transdermal patches, oral troches, or injections, must be off for 8 weeks or
more prior to baseline mammogram and RPFNA.
Exclusion Criteria for Screening
Conditions:
- Have a predisposition to or prior history of thromboembolism, deep venous thrombosis,
pulmonary embolism, stroke, or myocardial infarction. Note that individuals with a
prior septic embolus only with no evidence of a clotting disorder are not excluded if
cleared by their cardiologist or internist.
- Prior bilateral oophorectomy
- BRCA1/2 deleterious mutation
- LCIS specifically designated as pleomorphic in the pathology report
- Prior high-risk ER+ and/or PR+ DCIS, defined as high grade, > 2 cm in diameter or
diagnosed at age < 50.
- Prior DCIS with cancer cells at inked margin where there was not an additional
resection.
- Prior invasive breast cancer
- Prior invasive uterine or ovarian cancer
- Current renal or liver disease or clinically significant abnormalities of liver and
renal function tests.
- Known hypoparathyroidism or recent history of triglycerides > 300 mg/dl.
- Women are sufficiently distressed by their vasomotor symptoms, such that they do not
believe they would be able to remain on study for 6 months without additional
medications if their hot flashes were not relieved.
- Any other condition or intercurrent illness that in the opinion of the investigator
makes the woman a poor candidate for RPFNA or treatment with BZA+CE.
Medications
- Current anticoagulant use (must have discontinued for 3 weeks prior to FNA)
- Taking oral or transdermal systemic hormones within two months (eight weeks) prior to
baseline blood, imaging studies or RPFNA. (Note that continued use of vaginal low dose
hormonal preparations for dyspareunia is allowed if the woman had been on for at least
2 weeks prior to baseline testing)
- Taken tamoxifen, raloxifene, or an aromatase inhibitor within 6 months of baseline
blood imaging or RPFNA
Inclusion Criteria for Randomization Study mammograms
- 3D mammograms must be performed within 3 months of RPFNA. Women whose breast size
require mosaic views will not be eligible.
- Clinical mammogram Interpretation: Mammograms read out as Class 0 or IV must be
resolved with additional procedures prior to randomization or entry on intervention
phase. Women having a recent benign biopsy subsequent to a BIRADS IV mammogram with
continuing BIRADs IV on baseline mammogram for Volpara assessment may be entered if
other clinical assessments (i.e., MRI) is judged as not worrisome for cancer and/or
re-biopsy or re-excision is not being considered by the patient's clinical team.
- Raw data DICOM files must be available for generation of Volpara Score Card. Study
consent must be signed prior to sending the DICOM files to the researcher server as
these files will contain patient identifiers.
- A Volpara score card must be generated for at least 1 breast and the FGV must meet
minimal requirements for BMI.
- If BMI < 25 kg/m2, then FGV must average at least 20 cm3 per breast (i.e., ≥20 cm3 if
only one breast evaluable and ≥40 cm3 total if both breasts evaluable).
- If BMI is 25-38 kg/m2 then FGV must be at least 30 cm3 per breast (i.e., ≥30 cm3 if
only one breast evaluable and ≥60 cm3 total if both breasts evaluable).
- The Volpara® "Score Card" must be sent to KUMC prior to randomization.
RPFNA must be performed and specimen received at KUMC in good condition. RPFNA specimen
must have ductal/lobular epithelial cells on Thinprep® slides; but there is no requirement
for a specific cell number, value for Ki-67, or cytomorphology.
Blood must be drawn prior to randomization and sent to KUMC.
Complete Menopause specific quality of life questionnaire, information for hot flash score.
Willing to comply with study procedures.
Participants at KUMC: Dual energy x-ray absorptiometry (iDXA)
Pregnancy test for women <age 55 with intact uterus
Exclusion Criteria for Randomization Intercurrent illness which makes potential participant
unsuitable for study; Starting hormone replacement therapy (prescription pills, injections,
patches) between mammogram/RPFNA and enrollment on study.