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Completed

NCT Number: NCT00574301

Percutaneous Removal and Margin Ablation for Breast Cancer

We hypothesize that radiofrequency ablation after single-insertion image guided vacuum assisted biopsy (IVEB) can be used to achieve negative margins in small unicentric breast cancers (≤1.5 cm).

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Key information

Age range

18 year–90 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

University of Arkansas For Medical Sciences

Little Rock, Arkansas, 72205, United States

About this study

Using the Mammotome Breast Biopsy System (IVEB) in conjunction with MRI to predict extent of disease, ultrasound to direct removal of the tumor, touch preparation cytology for diagnosis, and ablation of margins using radiofrequency ablation (RFA), we propose to develop a comprehensive system for same-day diagnosis and treatment of patients with small breast lesions.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female, 18 to 90 years of age
  • Non-pregnant, not breastfeeding
  • Pre-study documentation of:
  • Size ≤1.5 cm cancer successfully removed by US-guided IVEB within 30 days of registration
  • Uni-centricity, unilateral cancer by radiology (mammogram and MRI)
  • Location of abnormality > 1 cm from the skin
  • Ductal Carcinoma, Invasive (Grade I-III) or In-Situ
  • No palpable axillary or supraclavicular lymph nodes
  • Good general health
  • Zubrod Performance Status of 0, 1, or 2
  • If prior non-breast malignancy, must have 5 year disease-free survival
  • No prior chemotherapy
  • Hormonal therapy must be stopped
  • Therapy with tamoxifen must have been of 14 days or less duration

Exclusion criteria

  • Subjects less than 18 years of age or greater than 90 years of age
  • Pregnant or breastfeeding
  • Male
  • Prior Breast Biopsy affected breast
  • Breast implants
  • Multicentric disease, bilateral disease
  • Residual disease after IVEB of > 1cm on MRI
  • Lesions > 1.5 cm in diameter
  • Lesions < 1 cm from skin surface
  • Previous radiation therapy to the breast

Treatment and study plan

Percutaneous Removal and Margin Ablation

Procedure

Patients with a diagnosis of unicentric invasive breast cancer diagnosed by IVEB will then be assigned to the next available surgery date. On that day, the patient's axillary staging will be done, followed by ablation of the biopsy cavity using RFA. The breast surgery may include lumpectomy (which will be directed with US-guidance to assure more accurate removal of the en bloc IVEB site and the margin zone of ablation) or simple mastectomy with or without reconstruction. The tissue specimen will be sent immediately from the operating room to Pathology for routine processing.

Other names: Mammotome Breast Biopsy System (IVEB), Ethicon Endo-Surgery, Radiofrequency Ablation (RFA), RITA Medical Systems, Lumpectomy, Mastectomy

Primary outcomes

  1. To quantify the degree of tumor-free margin achieved with image-guided vacuum assisted biopsy followed by ablation with radiofrequency ablation

    Time frame: Post-surgical pathology review

Secondary outcomes

  1. The proportion of patients with viable tumor cells beyond the margin

    Time frame: Post-surgical pathology review

Sponsors and collaborators

Lead sponsor

University of Arkansas

Other

Collaborators

  • Department of Health and Human Services
  • Ethicon Endo-Surgery
  • RITA Medical Systems

Registry information

Important dates

Study start
2002
Primary completion
2007
Study completion
2011
First posted
Dec 17, 2007
Registry last updated
Jul 25, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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