Preoperative and Intraoperative Quantification of Axillary Tumoral Load
NCT ID: NCT02197949
Last Updated: 2016-11-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
12 participants
OBSERVATIONAL
2014-07-31
2016-03-31
Brief Summary
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Despite these facts, a high proportion of patients with a positive axilla at diagnosis and submitted to level I and II axillary lymph node dissection show few lymph nodes infiltrated in the pathological study, frequently four or less neoplastic nodes. New methods of detecting these patients with limited infiltrated nodes should be developed and new approaches to axillary surgery (i.e., partial resection) should be offered.
To date, the only information expected to get after an axillary imaging is performed is if the axilla is infiltrated or not. No information about the tumoral load is demanded. In the other hand, level I and II ALND is performed according to established anatomic limits, without selecting the nodes to be excised neither identifying the ones infiltrated for a directed excision.
The aim of the study is to evaluate the ability of a specified and reproducible imaging protocol for distinguishing patients with a high axillary tumoral load from the ones with a low tumoral load. At the same time, as the initial nodes receiving lymph drainage should be the ones commonly affected, identifying these nodes injecting diluted methylene blue in the retroareolar parenchyma and studying their tumoral load could help selecting patients with high from those with low axillary tumoral load.
Evaluation of both steps (that is, first the imaging protocol followed by the methylene blue protocol), could eventually help to distinguish which patients should be submitted to a classical level I and II ALND and which ones can be spared from excising the lymph nodes not stained by the methylene blue.
Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Breast cancer patients with infiltrated axillary l
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Older than 18 years old
* Able to understand and accept the protocol procedure and to sign an informed consent form in accordance with national legislation.
Exclusion Criteria
* Patients younger than 18 years old.
* Psychiatric disease
* Difficulties to understand Spanish.
18 Years
ALL
No
Sponsors
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Parc de Salut Mar
OTHER
Responsible Party
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Maria del Mar Vernet
MD
Principal Investigators
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Maria del Mar Vernet, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Parc de Salut Mar
Locations
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Hospital del Mar
Barcelona, Barcelona, Spain
Countries
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Other Identifiers
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ELISA
Identifier Type: -
Identifier Source: org_study_id