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

Breast Cancer Staging MAgnetic Resonance for Treatment (B-SMART)

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00948285
Acronym
BSMART
Enrollment
194
Registered
2009-07-29
Start date
2009-07-31
Completion date
2018-12-31
Last updated
2019-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

breast cancer, magnetic resonance imaging

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.

Interventions

PROCEDUREMRI

magnetic resonance imaging (MRI)

Sponsors

Texas Tech University Health Sciences Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 99 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
A difference of 10% in the margin revision rate in women undergoing breast conservation for cancer.3 years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026