跳至主要内容
临床试验/NCT02456649
NCT02456649已完成不适用

A Phase II Study of the Outcomes of Intraoperative Margin Assessment With Adjunctive Use of MarginProbe in Addition to Standard

Huntington Memorial Hospital2 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2015年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
64
试验地点
2
主要终点
Percentage of patients with histologically positive surgical margins

研究概览

简要总结

The combination of breast conserving surgery (lumpectomy) with radiation therapy has been shown to result in equivalent overall survival rates compared to mastectomy for the local treatment of breast cancer. As a result, the majority of patients diagnosed with breast cancer in the United States undergo lumpectomy as their primary surgical therapy. Multiple studies have demonstrated the association between positive lumpectomy margins and an increased risk of ipsilateral breast tumor recurrence, even with postoperative radiation. Studies report 20-40% of lumpectomy procedures result in one or more involved (positive) surgical margins, leading to the need for further surgery, emotional distress, poorer cosmesis, delay to adjuvant treatments, and increased cost. Current available intraoperative margin assessment techniques include specimen Xray, gross pathology, frozen section, and touch prep cytology. To reduce the incidence of positive margins, the MarginProbe (Dune Medical Devices, Caesarea, Israel) was developed to provide real-time, intraoperative assessment of the presence of tumor at the lumpectomy margin. In the current study, the investigators aim to determine the effectiveness of MarginProbe as an adjunctive tool to standard practice for intraoperative identification of tumor at lumpectomy margins, and its ability to reduce positive margins and decrease the need for additional surgical procedures.

详细描述

In the current study, the investigators aim to determine the effectiveness of MarginProbe as an adjunctive tool to standard practice for intraoperative identification of tumor at lumpectomy margins, and its ability to reduce positive margins and decrease the need for additional surgical procedures.

Aims of the study:

Primary objectives

  1. Determine positive margin rate following lumpectomy

Secondary objectives

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

性别
Female
接受健康志愿者

入选标准

  • Subjects able to read and understand the informed consent

排除标准

  • Subjects unable to read or understand the informed consent.

结局指标

主要结局

Percentage of patients with histologically positive surgical margins

时间窗: 2 weeks after surgery

次要结局

  • Percentage of patients who undergo a second surgery after initial lumpectomy.(2 weeks after surgery)
  • False positive and false negative rate of Intraop MarginProbe results compared to histologic evaluation(2 weeks after surgery)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jeannie Shen

Medical director, Breast Surgery

Huntington Memorial Hospital

研究点 (2)

Loading locations...

相似试验