Axillary Reverse Mapping
- Conditions
- Cancer of the Breast
- Interventions
- Procedure: Axillary Reverse Mapping
- Registration Number
- NCT00572481
- Lead Sponsor
- University of Arkansas
- Brief Summary
We hypothesize that variations in anatomic location of the arm lymphatic drainage system put the arm lymphatics at risk for disruption during a SLNB and / or ALND. Therefore, mapping the drainage of the arm during the procedure would decrease the likelihood of inadvertent disruption of the lymphatics and the subsequent development of lymphedema. A combination of radioactivity and blue dye will be used.
- Detailed Description
Mapping Procedure:
Each patient will receive an injection of 1.0 mCi of technetium-99m sulfur colloid into the normal breast tissue surrounding the primary cancer or biopsy cavity directed subareolar or around the tumor.
If the radioactive SLN cannot be located prior to incision via gamma probe then the blue dye will be used in the breast either in the subareolar plexus or peritumorally at the discretion of the surgeon. For this contingency (expected to occur \<3% of the time), the blue dye will be used in the breast (and NOT the arm), as the prime concern is locating the SLN for staging.
If the blue dye is unnecessary to find the sentinel node draining from the breast, then it will be injected dermally in the upper inner arm along the Biceps groove of the ipsilateral arm in order to locate the draining lymphatics from the arm. No more than 5cc of blue dye will be injected in either the subareolar plexus, peritumorally (intraparenchymal or dermally), or dermally in the patient's ipsilateral arm dependent upon the contingencies stated above. Site of all injections (radioactivity and/or blue dye) will be recorded.
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 1000
- 18-100 years old
- Not pregnant or breastfeeding
- Breast cancer requiring lymph node evaluation for the ipsilateral or contralateral breast OR prophylactic mastectomy
- Willing participation following an informed consent process
- Patient < 18 y/o or > 100 y/o
- Pregnant or breastfeeding
- If a pregnant female should be diagnosed with breast cancer an exception would be considered on a case to case basis.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Sentinel Lymph Node Biopsy Only Axillary Reverse Mapping Axillary Reverse Mapping Full Axillary Lymph Node Dissection Axillary Reverse Mapping Axillary Reverse Mapping
- Primary Outcome Measures
Name Time Method Occurrence of lymphedema by the first year following surgery One year An occurrence will consist of an increase of 20% or more in ipsilateral arm volume over the pre-surgery volume, and be accompanied by a confirmatory diagnosis of lymphedema from the UAMS lymphedema clinic.
- Secondary Outcome Measures
Name Time Method Successful protection of the arm lymphatics during SLNB and/or ALND. Time of surgery successful avoidance of resection and/or successful preservation of structural integrity of arm lymphatics during the surgical procedure.
Occurrence of crossover (i.e., co-localization) between hot breast SLN and blue arm lymphatics. Time of surgery A crossover event will consist of identification of one or more lymph nodes that are both focally radioactive following peritumoral Tc99m injection and noticeably stained blue following ipsilateral arm injection with Lymphazurin.
Characterization of location (typical versus variant) of arm lymphatics. Time of surgery brief location details will also be collected.
Successful identification (i.e., localization) of breast SLN and arm lymphatics Time of surgery successful localization of one or more lymph nodes to which the peritumoral breast region drains
Trial Locations
- Locations (1)
University of Arkansas For Medical Sciences
🇺🇸Little Rock, Arkansas, United States