Importance of Magnetic Resonance Imaging (MRI) in Treating Breast Cancer

NCT ID: NCT00948285

Last Updated: 2019-11-13

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 194 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-07-31
• Study Completion Date: 2018-12-31

Brief Summary

The purpose of this study is to determine if the use of magnetic resonance imaging (MRI) for breast cancer translates into better surgical outcomes. MRIs may help ensure that as little healthy tissue is removed as is possible and may help prevent the need for additional surgical procedures.

Detailed Description

We propose that the role of preoperative staging-MRI in breast cancer be studied by following the occurrence of negative margins at first surgery and the volume of resection in a randomized prospective study. The need for re-excision is an objective marker of satisfactory local surgery and is available as soon as the final pathology report is back. We propose that the closest margin and the rate of re-excision be used as the primary outcome measures to evaluate the contribution of MRI. In addition, since cosmetic preservation is one of the goals of breast conservation, we propose that cosmetic outcome be used as the secondary outcome measure. The visual analogue scale for cosmetic outcome varies between observers and with time; however, the volume of tissue that is excised is an objective surrogate of cosmetic outcome.15 Since the excised volume is dictated by the tumor volume, the only variable under the surgeon's control is the volume of benign tissue excised in order to obtain negative margins. Hence, in this study, we propose to use a volume index of excised margins as an outcome measure for cosmesis. The index value will be calculated for each subject by adding the two measurements of benign margin for each of the three dimensions measured and multiplying them to produce a volume index for each subject.

Conditions

Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

MRI

Preoperative staging with mammogram, ultrasound, and MRI, followed by surgery (n=200)

Group Type: EXPERIMENTAL

MRI

Intervention Type: PROCEDURE

magnetic resonance imaging (MRI)

Non-MRI

Preoperative staging with mammogram and ultrasound alone, followed by surgery (n=200)

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

MRI

magnetic resonance imaging (MRI)

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• Newly diagnosed breast cancer patients
• Breast cancer patients identified as conservation candidates by their surgeons

Exclusion Criteria

• Patients with a history of prior breast cancer treatment (recurrence)
• Patients with breast cancer diagnosis during pregnancy (women who could bear children must have a negative pregnancy test before beginning this study)
• Patients with documented sensitivity to gadolinium (contrast agent used during MRI)
• Patients who weigh more than 350 pounds (weight limit on MRI machine)
• Patients who receive neoadjuvant chemotherapy
• Patients with renal insufficiency (serum Cr > 1.5) due to the danger of nephrogenic systemic sclerosis with the administration of Gadolinium

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 99 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Texas Tech University Health Sciences Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Rakhshanda L Rahman, MD

Role: PRINCIPAL_INVESTIGATOR

Texas Tech University Health Sciences Center

Locations

Texas Tech University Health Sciences Center School of Medicine

Amarillo, Texas, United States

Countries

United States

Other Identifiers

A09-3519

Identifier Type: -

Identifier Source: org_study_id