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临床试验/NCT02564848
NCT02564848进行中(未招募)不适用

IIT2015-06-Chung: Safety and Efficacy of Omission of Sentinel Node Biopsy in Patients With Clinical T1-2 Estrogen-Positive Breast Cancer Over Age 65

Cedars-Sinai Medical Center1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2016年1月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
200
试验地点
1
主要终点
Regional recurrence

研究概览

简要总结

This study will examine the outcomes of lumpectomy, surgery to remove a tumor, without sentinel node biopsy (SNB) for women at least 65 years of age with clinically node-negative breast cancer. Clinically node-negative means that during a physical exam your doctor cannot feel or see that any lymph nodes near the breast area are swollen and there is also no imaging evidence, such as from a mammogram, of nodal involvement.

详细描述

The primary objective of the study is to determine whether omission of sentinel node biopsy in patients who meet eligibility criteria results in an acceptable regional recurrence rate over a 6-year period. A regional recurrence is defined as any recurrence in the ipsilateral axillary nodes, supraclavicular nodes or internal mammary nodes.

Eligible patients will undergo standard of care lumpectomy without sentinel node biopsy followed by radiation and hormonal therapy or have already undergone the procedure prior to enrollment in the study. She may also receive chemotherapy as determined by her treating physician. 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
65 Years 至 —(Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Female age 65 and older
  • •Patients enrolled prior to surgery: Diagnosis of clinical T1-2N0, ER+, HER2-negative, invasive breast cancer as determined by treating physician. DCIS or LCIS may be present with invasive cancer.
  • •Patients enrolled after surgery: pT1-2NX, or pT1-2N0, ER+, HER2-negative, invasive breast cancer. DCIS or LCIS may be present with invasive cancer.
  • •Plan to undergo lumpectomy within 3 months of study registration, or underwent lumpectomy within 60 days of study registration (without sentinel node biopsy)
  • •Patients in whom lymph nodes are palpable and not suspicious who are found to be nodal tumor-free by nodal core needle biopsy are permitted, but those with biopsy-proven nodal metastases are excluded

排除标准

  • •Patients with diagnosis of ductal or lobular carcinoma in situ
  • •Patients with diagnosis of inflammatory breast cancer
  • •Patients who have undergone neoadjuvant chemotherapy for current primary breast cancer (past treatments for other cancers are acceptable)
  • •Patients planning to have mastectomy or had a mastectomy of the ipsilateral breast
  • •Prior history of ipsilateral (invasive or DCIS) breast cancer
  • •Diagnosis of clinical T3 or T4 breast cancer

研究组 & 干预措施

Lumpectomy without sentinel node biopsy

Experimental

Subjects will undergo standard of care lumpectomy. A biopsy of the sentinel node will not be performed. After surgery, subjects will receive standard of care radiation on the affected breast and hormonal therapy.

干预措施: Lumpectomy without sentinel node biopsy (Procedure)

结局指标

主要结局

Regional recurrence

时间窗: A regional recurrence during six years of follow-up after lumpectomy.

A regional recurrence is defined as any recurrence in the ipsilateral axillary nodes, supraclavicular nodes or internal mammary nodes and will be determined by physical exam and breast imaging

次要结局

  • Overall survival(From date of diagnosis until the date of death from any cause assessed up to 5 years.)
  • Disease-free survival(From date of diagnosis until the date of locoregional or distant recurrence assessed up to 5 years.)

研究者

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

Alice Chung

Assistant Professor of Surgery

Cedars-Sinai Medical Center

研究点 (1)

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