Excision Followed by Radiofrequency Ablation for Breast Cancer
Status: | Active, not recruiting |
---|---|
Conditions: | Breast Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 50 - 100 |
Updated: | 7/1/2018 |
Start Date: | June 2010 |
End Date: | June 2020 |
ABLATE Registry: Radiofrequency Ablation After Breast Lumpectomy (eRFA) Added To Extend Intraoperative Margins in the Treatment of Breast Cancer
The purpose of this study will be to evaluate, in a multi-center setting, the ability of
radiofrequency ablation (RFA) of breast cancer lumpectomy sites to extend the "final"
negative margin and consequently decrease the rates of re-operation. During the initial
breast conservation procedure (lumpectomy), immediately following routine surgical resection
of the tumor, radiofrequency energy (RFA) is applied to the wall (bed) of the fresh
lumpectomy cavity, thus extending tumor free margin radially beyond the volume of the
resected specimen.
radiofrequency ablation (RFA) of breast cancer lumpectomy sites to extend the "final"
negative margin and consequently decrease the rates of re-operation. During the initial
breast conservation procedure (lumpectomy), immediately following routine surgical resection
of the tumor, radiofrequency energy (RFA) is applied to the wall (bed) of the fresh
lumpectomy cavity, thus extending tumor free margin radially beyond the volume of the
resected specimen.
Inclusion Criteria:
- Patient is a female, ≥ 50 years of age
- The tumor size is ≤ 3 cm (on pre-study radiologic OR clinical exam)
- The tumor is unicentric and unilateral
- The tumor is not involving the skin
- Pathology confirms ductal in situ (DCIS) OR infiltrating ductal carcinoma (IDC), grade
I-III
- If tumor is IDC, pathology must be hormone receptor positive (ER+ and/or PR+)
- Patient signs current written informed consent and HIPAA forms
Exclusion Criteria:
- Patient is under 50 years of age
- Patient is male
- Tumor > 3 cm in diameter
- Bilateral malignancy
- Clinically positive lymph nodes
- Tumor involving the skin
- Pathology confirms invasive lobular carcinoma
- Breast implants
- Less than 2 years disease-free survival from previous breast cancer
- Neoadjuvant chemotherapy or chemotherapy for another breast cancer within two years
We found this trial at
6
sites
New York, New York 10032
Principal Investigator: Sheldon Marc Feldman, MD
Phone: 212-305-6679
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529 West Markham Street
Little Rock, Arkansas 72205
Little Rock, Arkansas 72205
(501) 686-7000
Principal Investigator: Daniela Ochoa, MD
University of Arkansas for Medical Sciences The University of Arkansas for Medical Sciences (UAMS) in...
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Denver, Colorado 80218
Principal Investigator: Julie Barone, DO, FACS
Phone: 303-318-2271
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San Diego, California 92123
Principal Investigator: Robert Barone, DO
Phone: 858-939-5052
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Tucson, Arizona 85721
(520) 621-2211
Principal Investigator: Rebecca Viscusi, MD
Phone: 520-694-2873
University of Arizona The University of Arizona is a premier, public research university. Established in...
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Westwood, Kansas 66205
Principal Investigator: Marilee McGinness, MD
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