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临床试验/NCT02610621
NCT02610621撤回2 期

IIT2015-11-Giuliano: Safety and Efficacy of Omission of Sentinel Node Biopsy for Breast Cancer Patients Who Plan to Have Adjuvant Chemotherapy

Cedars-Sinai Medical Center2 个研究点 分布在 1 个国家开始时间: 2015年12月最近更新:
适应症

试验速览

阶段
2 期
状态
撤回
试验地点
2
主要终点
A determination of the locoregional recurrence rate in patients with clinically node negative T1 and T2 breast cancer treated with systematic chemotherapy and whole breast radiation in whom sentinel node biopsy is not performed

研究概览

简要总结

Eligible patients will be female, ages 18 and older and have a diagnosis of Clinical T1 or T2 invasive breast cancer with no suspicious palpable adenopathy. Patients will undergo standard of care lumpectomy without sentinel node biopsy and whole breast radiation, followed by chemotherapy.

Sentinel node biopsy is also considered standard care when patients have localized breast cancer. Treatment can often be influenced by whether the results of the biopsy show cancer or not. However, the biologic factors of the primary tumor have become more important in determining treatment recommendations in women with clinically node negative breast cancer.

详细描述

The primary objective of the study is to determine the locoregional recurrence rate in patients with clinically node negative T1 and T2 breast cancer treated with systemic chemotherapy and whole breast irradiation in whom biopsy of the sentinel node is not performed. A locoregional recurrence is defined as any recurrence in the ipsilateral axillary nodes or in the supraclavicular nodes.

After surgery, a patient will receive standard of care radiation on her affected breast and chemotherapy. A physical examination of the affected breast and regional lymph nodes will be conducted every six months for the first two years of follow up and then yearly for the last 3 years of follow up. Imaging of the affected breast will occur every 12 months after surgery per standard of care.

研究设计

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

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Female age 18 and older, not pregnant or lactating
  • Clinical T1 or T2 invasive cancer with no suspicious palpable adenopathy
  • If abnormal axillary nodes are seen on preoperative imaging, a negative fine needle aspiration or core biopsy is required for study entry.
  • Planned treatment with breast conserving surgery and whole breast irradiation
  • Chemotherapy required postoperatively based on patient and tumor characteristics at diagnosis

排除标准

  • Patients with suspicious palpable axillary adenopathy
  • Patients with biopsy demonstrating axillary nodal metastases
  • Patients with treatment by mastectomy
  • Patients who have undergone neoadjuvant chemotherapy
  • Patients with co-morbidities rendering the patient not a candidate for chemotherapy, surgery, or irradiation
  • Patients treated with accelerated partial breast irradiation (APBI)
  • Patients with contraindication to radiation

结局指标

主要结局

A determination of the locoregional recurrence rate in patients with clinically node negative T1 and T2 breast cancer treated with systematic chemotherapy and whole breast radiation in whom sentinel node biopsy is not performed

时间窗: Assessed up to 5 years from date of lumpectomy

次要结局

未报告次要终点

研究者

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

Armando Giuliano

Professor of Surgery

Cedars-Sinai Medical Center

研究点 (2)

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