NL-OMON38406
Completed
Not Applicable
Comparison of pre- and postoperative clinical target volumes at CT and MRI imaging in breast-conserving therapy: A prospective cohort study. - Clinical target volumes in breast-conserving therapy.
niversitair Medisch Centrum Utrecht0 sites27 target enrollmentTBD
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- breast cancer
- Sponsor
- niversitair Medisch Centrum Utrecht
- Enrollment
- 27
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- Female gender;
- •\- Age \>\= 18 years,
- •\- cT1\-T2N0\-1M0 breast cancer;
- •\- Scheduled for breast\-conserving therapy;
- •\- Before breast\-conserving surgery;
- •\- Written informed consent.
Exclusion Criteria
- •\- Legal incapability;
- •\- Insufficient command of the Dutch language;
- •\- History of ipsilateral breast surgery (benign, malign, augmentation, reduction);
- •\- Inability to maintain the standard supine RT treatment position for 30 minutes;
- •\- Exclusion criteria for MRI following the protocol of the department of radiology UMCU;
- •\- GFR of \<45mL/min/1\.73m2\. In patients with known risk factors a minimum GFR of \<60mL/min/1\.73m2 will be required, according to the UMCU protocol;
- •\- Iodine allergy (contraindication for iodine\-based intravenous contrast agents);
- •\- Treated with neo\-adjuvant chemotherapy.
- •\- Treated with modified radical mastectomy.
- •\- Treated with en\-block axillary lymph node dissection.
Outcomes
Primary Outcomes
Not specified
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