Overview

This trial is active, not recruiting.

Condition ductal breast carcinoma in situ
Treatments magnetic resonance imaging, therapeutic conventional surgery, therapeutic surgical procedure, radiation therapy, endocrine therapy, quality-of-life assessment, laboratory biomarker analysis, cytology specimen collection procedure
Sponsor ECOG-ACRIN Cancer Research Group
Collaborator National Cancer Institute (NCI)
Start date March 2015
End date November 2027
Trial size 350 participants
Trial identifier NCT02352883, E4112, ECOG-E4112, NCI-2014-01261, U10CA037403, UG1CA189828

Summary

This clinical trial studies magnetic resonance imaging (MRI) and gene expression in diagnosing patients with abnormal cells in the breast duct that have not spread outside the duct. MRI uses radio waves and a powerful magnet linked to a computer to create detailed pictures of areas inside the body. MRI may help find and diagnose patients with breast cancer. It may also help doctors predict a patient's response to treatment and help plan the best treatment. Genetic studies may help doctors predict the outcome of treatment and the risk for disease recurrence. Performing MRI with genetic studies may help determine the best treatment for patients with breast cancer in situ.

United States Delaware, Kansas, Louisiana, New York, North Carolina, Pennsylvania, and Washington
Other Countries No locations recruiting

Study Design

Allocation non-randomized
Endpoint classification efficacy study
Intervention model crossover assignment
Masking open label
Primary purpose diagnostic
Arm
(Experimental)
Patients undergo MRI prior to surgery. Patients undergo additional imaging and/or biopsies if indicated based on MRI.
magnetic resonance imaging Magnetic Resonance Imaging
Undergo MRI
quality-of-life assessment Quality of Life Assessment
Ancillary studies
laboratory biomarker analysis
Correlative studies
cytology specimen collection procedure Cytologic Sampling
Correlative studies
(Experimental)
Patients undergo a mastectomy. Patients do not register for Step 3.
therapeutic conventional surgery
Undergo mastectomy
quality-of-life assessment Quality of Life Assessment
Ancillary studies
laboratory biomarker analysis
Correlative studies
cytology specimen collection procedure Cytologic Sampling
Correlative studies
(Experimental)
Patients undergo wide local excision +/- re-excision. Patients may cross-over to Arm B if mastectomy is indicated. Tissue samples collected during surgery are used to calculate the DCIS score using genetic analysis testing. Patients may then proceed to Step 3.
therapeutic surgical procedure
Undergo wide local excision
quality-of-life assessment Quality of Life Assessment
Ancillary studies
laboratory biomarker analysis
Correlative studies
cytology specimen collection procedure Cytologic Sampling
Correlative studies
(Experimental)
Patients undergo endocrine therapy as directed.
endocrine therapy Chemotherapy-Hormones/Steroids
Undergo endocrine therapy
quality-of-life assessment Quality of Life Assessment
Ancillary studies
laboratory biomarker analysis
Correlative studies
cytology specimen collection procedure Cytologic Sampling
Correlative studies
(Experimental)
Patients undergo radiation therapy and endocrine therapy as directed.
radiation therapy Cancer Radiotherapy
Undergo radiation therapy
endocrine therapy Chemotherapy-Hormones/Steroids
Undergo endocrine therapy
quality-of-life assessment Quality of Life Assessment
Ancillary studies
laboratory biomarker analysis
Correlative studies

Primary Outcomes

Measure
Proportion of patients judged to be breast conservation candidates based upon standard imaging and physical examination who convert to mastectomy in step 1 based on MRI findings
time frame: After MRI (within 30 days following study entry), and prior to surgery
Proportion of patients judged to be breast conservation candidates based upon standard imaging and physical examination who have a mastectomy as the final surgical procedure in step 2
time frame: Up to 12 months post-op

Secondary Outcomes

Measure
Factors associated with DCIS score
time frame: After surgery (DCIS Score is determined from surgical specimen)
Diagnostic accuracy of MRI in extent of disease evaluation in patients with DCIS
time frame: Up to 12 months post-op
Proportion of patients who require re-operation because of inadequate excision after MRI
time frame: Up to 12 months post-op
Proportion of patients who proceed to mastectomy after an initial attempt at wide local excision because of either inadequate tumor-free margins (< 2mm), or other reasons
time frame: Up to 12 months post-op
IBE rate
time frame: At 5 years
IBE rate
time frame: At 10 years
Proportion of women who receive treatment that is concordant with their treatment goals and concerns
time frame: Up to 24 months post-op
Proportion of women whose decision autonomy preference was concordant with perceived level of decision involvement
time frame: Up to 5 days after pre-surgical consultation
Decision quality, assessed using the composite of knowledge score and decision process score
time frame: Up to 5 days after pre-surgical consultation
Role of concordance between decision autonomy preference and perceived level of decision involvement, knowledge and decision process scores as independent predictors of decision satisfaction
time frame: Assessed via questionnaire administered at first post-operative visit
Patient-reported quality of life, measured using the Patient Reported Outcomes Measurement Information System (PROMIS)10 instrument
time frame: At 12 months post-op
Patient-reported quality of life, measured using the PROMIS10 instrument
time frame: At 24 months post-op
Role of disease status, diagnostic test results, and surgeon recommendation as predictors of treatment received
time frame: Up to 24 months post-op
Patient-reported diagnostic testing burden of bilateral mammogram, MRI, and biopsies, measured by TMI
time frame: Up to 5 days after pre-surgical consultation

Eligibility Criteria

Female participants at least 18 years old.

Inclusion Criteria: - Registration to Step 1: - Patients must have pathologically confirmed diagnosis of unilateral ductal carcinoma in situ with no evidence of microinvasive or invasive disease obtained by core needle biopsy within 4 months of registration; patients diagnosed by surgical excision are not eligible; patients with synchronous bilateral disease are not eligible; patients with synchronous bilateral disease (i.e., synchronous DCIS or invasive cancer) are not eligible - Patients will be staged prior to registration according to the clinical staging criteria adapted from the American Joint Committee on Cancer (AJCC) Cancer Staging Data Forms of the AJCC Cancer Staging Manual, 7th Edition, 2009; Note: For consistency purposes, AJCC 7th Edition will continue to be used throughout the entire study enrollment period - Required studies include a bilateral screening mammogram within 6 months and diagnostic mammogram of the affected breast within 3 months prior to registration - Patients must not have previous ipsilateral invasive breast cancer or DCIS - Patients must not have known deleterious mutations in breast cancer (BRCA) genes - Patients must not have received hormonal therapy (i.e., tamoxifen, raloxifene, and/or aromatase inhibitors) for prevention of breast cancer within 3 months of the biopsy documenting DCIS - Patients must not have history of chemotherapy for cancer within 6 months prior to registration - No prior history of breast radiotherapy that will prevent the use of radiotherapy for the present DCIS - Patients must be judged to be suitable to undergo MRI and receive the contrast agent gadolinium (exclusions follow): - No history of untreatable claustrophobia; - No presence of metallic objects or implanted medical devices in body (i.e., cardiac pacemaker, aneurysm clips, surgical clips, prostheses, artificial hearts, valves with steel parts, metal fragments, shrapnel, tattoos near the eye, or steel implants); - No history of sickle cell disease; - No contraindication to intravenous contrast administration; - No known allergy-like reaction to gadolinium or moderate or severe allergic reactions to one or more allergens as defined by the American College of Radiology (ACR); patient may be eligible if willing to undergo pre-treatment as defined by the institution's policy and/or ACR guidance; - No findings consistent with renal failure, as determined by glomerular filtration rate (GFR) < 30 mL/min/1.73 m^2 based on a serum creatinine level obtained within 28 days prior to registration; - Weight lower than that allowable by the MRI table; - No prior MRI of the breasts within the 6 months prior to registration - Patients must be eligible for breast-conserving therapy (BCT) based on clinical examination and mammography; if ultrasound is performed, findings must also be consistent with eligibility for BCT - Patients must not have multicentric disease scheduled to undergo multiple lumpectomies; multifocal disease that can be encompassed in a single operative bed are eligible - Women must not be pregnant or breast-feeding; all females of childbearing potential must have a blood test or urine study within 3 weeks prior to registration to rule out pregnancy; a female of childbearing potential is any woman, regardless of sexual orientation or whether they have undergone tubal ligation, who meets the following criteria: - Has not undergone a hysterectomy or bilateral oophorectomy; or - Has not been naturally postmenopausal for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months) - Women of childbearing potential must be strongly advised to use an accepted and effective method of contraception or to abstain from sexual intercourse for the duration of their participation in the study - Registration to Step 2: - MRI has been performed in Step 1, and additional imaging studies and biopsies performed if indicated - The clinician/patient has made the decision as to whether the patient will proceed to wide local excision or mastectomy - Registration to Step 3: - Patient's most recent surgery was wide local excision with or without re-excision and for which there was obtained clear (>= 2 mm) margins at breast conserving surgery, and the pathology reveals pure DCIS; patients with invasive cancer or DCIS with microinvasion will not be registered on step 3, but will be followed for clinical outcomes - The OncotypeDX Patient Report of the DCIS Score from the OncotypeDX Breast Cancer Assay performed by Genomic Health on the excision tissue have been uploaded by the site into the Rave electronic case report forms (eCRF)

Additional Information

Official title Prospective Study of Magnetic Resonance Imaging (MRI) and Multiparameter Gene Expression Assay in Ductal Carcinoma In Situ (DCIS)
Principal investigator Constance Lehman
Description PRIMARY OBJECTIVES: I. To estimate the proportion of patients with ductal carcinoma in situ (DCIS) diagnosed on core needle biopsy judged to be breast conservation candidates based upon standard imaging (mammography +/- sonography) and physical examination (a) who convert to mastectomy in step 1 based on MRI findings, and (b) who have a mastectomy as the final surgical procedure in step 2. SECONDARY OBJECTIVES: I. To assess the relation between baseline clinical covariates (e.g., tumor grade, necrosis, histologic type, mammographic lesion size), MRI morphologic and kinetic features, and the DCIS score. II. To assess the diagnostic accuracy of MRI in extent of disease evaluation in patients with DCIS. III. To estimate the proportion of patients who require re-operation because of inadequate excision after MRI. IV. To estimate the proportion of patients who proceed to mastectomy after an initial attempt at wide local excision because of either inadequate tumor-free margins (< 2 mm), or other reasons. V. To estimate the 5-year and 10-year ipsilateral breast event (in situ and invasive) rate (IBE) among women with DCIS assessed with MRI preoperatively and treated with wide local excision without radiation therapy (if there is a low DCIS score) or with radiation therapy (if there is an intermediate-high DCIS score). VI. To estimate the proportion of women with DCIS who receive treatment that is concordant with their treatment goals and concerns. VII. To estimate the proportion of women with DCIS whose decision autonomy preference was concordant with perceived level of decision involvement. VIII. To assess decision quality using knowledge score and decision process. IX. To assess concordance between decision autonomy preference and perceived level of decision involvement, knowledge and decision process scores as independent predictors of decision satisfaction at the first post-operative visit. X. To assess the relationship of patient-reported outcomes and disease-specific covariates, and quality of life after treatment. XI. To assess the role of disease status, diagnostic test results and surgeon recommendation as predictors of treatment received. XII. To compare the patient-reported diagnostic testing burden of bilateral mammography and MRI as measured by Testing Morbidities Index (TMI). OUTLINE: STEP 1: ARM A: Patients undergo MRI prior to surgery. Patients undergo additional imaging and/or biopsies if indicated based on MRI. STEP 2: Patients are assigned to 1 of 2 treatment arms based on the results of the MRI. ARM B: Patients undergo a mastectomy. Patients do not register for Step 3. ARM C: Patients undergo wide local excision +/- re-excision. Patients may cross-over to Arm B if mastectomy is indicated. Tissue samples collected during surgery are used to calculate the DCIS score using genetic analysis testing. Patients may then proceed to Step 3. STEP 3: Patients are assigned to 1 of 2 treatment arms based on the results of the DCIS score test. ARM D (DCIS score < 39): Patients undergo endocrine therapy as directed. ARM E (DCIS score >= 39): Patients undergo radiation therapy and endocrine therapy as directed. After completion of study treatment, patients are followed up every 6 months for 5 years and then every 12 months for 5 years.
Trial information was received from ClinicalTrials.gov and was last updated in September 2015.
Information provided to ClinicalTrials.gov by Eastern Cooperative Oncology Group.
Location data was received from the National Cancer Institute and was last updated in April 2016.