None listed
Conditions
Interventions
None listed
Sponsors
The Catholic University of Korea
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. 20~ 70 old aged woman (cancer detection time based) 2. histological confirmation of invasive breast cancer 3. margin negative result at the breast conserving surgery 4. underwent breast conserving surgery 6~12 months before 5. underwent mammography, ultrasonography, and breast MRI regularly 6~12
Exclusion criteria
Exclusion criteria: 1. GFR (glomerular filtration rate) < 30 mL/min/1.73m2, or known chronic renal failure 2. Acute renal insufficiency of any intensity, either due to hepato-renal syndrome or occurring in the perioperative liver transplantation period. 3. Distant metastasis at the time of breast conserving surgery 4. Pregnant or lactating women 5. History of contraindication of contrast enhanced MRI such as claustrophobia, hypersensitivity to intravenous contrast media 6. Contraindications to the use of Gd-containing contrast agents (including subjects who are suspected for or known to have NSF) 7. History of severe allergic or anaphylactoid reaction to any allergen including drugs and contrast agents. 8. Patients unable and/or unwilling to comply with treatment or study instructions.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To make assessment on change of breast parenchyma pattern between preoperative MRI and postoperative MRI after breast conserving therapy and chemotherapy. | — |
Secondary
| Measure | Time frame |
|---|---|
| To make assessment of effect of parenchyma enhancement pattern on the breast cancer detection rate | — |
Countries
Korea, Republic of
Contacts
Public ContactBong Joo Kang
The Catholic University of Korea
Outcome results
None listed