Screening MRI for Cancer Recurrence in Patients Treated With Breast Conserving Therapy

NCT ID: NCT01257152

Last Updated: 2016-04-20

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 754 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2010-12-31
• Study Completion Date: 2016-01-31

Brief Summary

A prospective, multicenter study:

• Primary objective: to assess the diagnostic yield of screening MRI compared to physical examination, mammography or ultrasonography in the detection of recurrence in patients treated with breast conserving therapy
• Secondary objective: to describe the size, type, grade, and nodal status of cancers seen only on MRI and to estimate the rate of benign biopsies and short interval follow-up induced only by MRI in this population.

Detailed Description

• Patients treated with breast conserving therapy will be followed for recurrence in the ipsilateral or contralateral breast by physical examination every six month and imaging studies performed annually.
• The imaging including mammography, physician-performed bilateral whole breast ultrasonography and a dynamic breast MRI with gadolinium-containing contrast medium will be performed according to a standard protocol. Interpretation will be conducted independently and classified according to the Breast Imaging Reporting and Data System (BI-RADS) by experienced radiologists.
• Definitive information about the presence of malignancy will be obtained by biopsy directed by the imaging method best depicting the lesion with 14-g or 11-g needle devices or needle localized excision. The absence of breast cancer was determined by means of biopsy, the absence of positive findings on repeat imaging and clinical examination, or both at follow-up.
• After three rounds of annual screening, the diagnostic yield of screening MRI compared to physical examination, mammography or ultrasonography will be assessed.

Conditions

Breast Neoplasms; Neoplasm Recurrence, Local

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Women ≥ 20 years in age;
• Women who underwent breast-conserving surgery for invasive breast cancer, whose final margins were negative and who finished radiation therapy at least 6 months prior to this study;
• No history of breast biopsy of the breast within 6 months prior to this study;
• Signed study-specific informed consent prior to registration;
• Has not had contralateral mastectomy;
• No known metastatic disease;
• Not pregnant or lactating;
• No present signs or symptoms of breast cancer [no palpable mass(es), bloody or spontaneous clear nipple discharge, axillary mass, or abnormal skin changes in the breast(s) or nipple(s)].
• No contraindications to MRI examination.
• No prior MRI, US or mammography within the 6 months prior to the study.

Exclusion Criteria

• Had a screening contrast-enhanced breast MRI within the past 24 months or diagnostic contrast-enhanced MRI on any study breasts within the past 12 months;
• Had breast surgery and/or a core biopsy on the study breast(s) performed within the prior 6 months on the study
• Currently receiving chemotherapy [with exception to participant with personal history of cancer, and on chemoprevention with Tamoxifen, Evista (Raloxifene), Arimidex (Anastrozole), Aromasin (Exemestane) or other aromatase inhibitor];
• Participant with severely impaired renal function with estimated glomerular filtration rate (GFR) < 30 mL/min/1.73m2 and/or on dialysis.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Seoul National University Hospital

OTHER

Sponsor Role: lead

Responsible Party

Woo Kyung Moon

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Woo Kyung Moon, M.D., Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Department of Radiology, Seoul National University Hospital

Locations

Seoul National University Hospital

Seoul, , South Korea

Countries

South Korea

Other Identifiers

Screening MR for Recurred BrCa

Identifier Type: -

Identifier Source: org_study_id