Accuracy of FNA Versus CNB of Abnormal Axillary Lymph Nodes in Setting of Invasive Breast Cancer
Status: | Recruiting |
---|---|
Conditions: | Breast Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 10/13/2018 |
Start Date: | February 2014 |
End Date: | December 2020 |
Contact: | Nicole Winkler, MD |
Email: | nicole.winkler@hsc.utah.edu |
Phone: | 801-587-4309 |
Ultrasound Guided Core Needle Biopsy Versus Fine Needle Aspiration of Morphologically Abnormal Axillary Lymph Node in Patients With New Diagnosis or Suspected Diagnosis of Invasive Breast Carcinoma
To compare accuracy of ultrasound guided fine needle aspiration (FNA) to core needle biopsy
(CNB) of ultrasound detected abnormal axillary lymph nodes in patients with newly diagnosed
invasive breast cancer or suspected invasive breast cancer.
Hypothesis: FNA and CNB have equivalent diagnostic accuracies
In order to prove our hypothesis, we will perform FNA and CNB on the same lymph node in each
consented patient. The two samples will be evaluated separately by different pathologists
blinded to the material in the other sample.
The results of the biopsies will be compared to the gold standard (lymph node excision).
(CNB) of ultrasound detected abnormal axillary lymph nodes in patients with newly diagnosed
invasive breast cancer or suspected invasive breast cancer.
Hypothesis: FNA and CNB have equivalent diagnostic accuracies
In order to prove our hypothesis, we will perform FNA and CNB on the same lymph node in each
consented patient. The two samples will be evaluated separately by different pathologists
blinded to the material in the other sample.
The results of the biopsies will be compared to the gold standard (lymph node excision).
Inclusion Criteria:
- Recent or suspected diagnosis of invasive breast cancer with abnormal ipsilateral
axillary lymph node
- Able to provide informed consent
Exclusion Criteria:
- Lymph node not amenable to core biopsy
- Patient is unlikely to undergo lymph node excision (i.e. elderly patient with
co-morbidities)
We found this trial at
1
site
Salt Lake City, Utah 84112
Principal Investigator: Nicole Winkler, MD
Phone: 801-587-4602
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