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临床试验/JPRN-jRCTs061220113
JPRN-jRCTs061220113招募中2 期

Feasibility study of Tailored axillary surgery (TAS) for clinical node-positive breast cancer patients.

Shien Tadahiko0 个研究点目标入组 300 人开始时间: 2023年3月29日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
300

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 18age old 至 <= 74age old(—)
性别
Female

入选标准

  • Those who meet all of the following criteria are eligible
  • 1 Histologically diagnosed invasive breast cancer in the primary lesion of breast cancer
  • 2 Surgery is scheduled as initial treatment
  • 3 The lymph node most suspected of metastasis is pathologically diagnosed as metastasis by cytology or needle biopsy
  • 4 There are 1 3 lymph nodes suspected of metastasis in diagnostic imaging
  • 5 No suspicion of metastasis in all levels II III Rotter endothorax and supracraclavicular lymph nodes
  • 6 The clinical classification of the primary tumor is T1 3
  • 7 Women who are at least 18 years old and 74 years of age or younger on the date of registration
  • 8 Performance status is 0 or 1 in the ECOG criterion
  • 9 The test value within 28 days before registration satisfies
  • 10 Bilateral breast cancer regardless of metachronous or simultaneity
  • 11 Patients can receive standard radiotherapy and systemic drug therapy after surgery
  • 12 Written consent has been obtained from the patient to participate in the study

排除标准

  • 1 Active multiple cancers (simultaneous double cancers/multiple cancers and metachronous duplication with a disease-free period of up to 5 years)
  • Cancer/Multiple Carcinoma. However, even if the disease-free period is less than 5 years, the patient has a complete response to radiation therapy.
  • History of stage 0 beds, stage I laryngeal cancer, or cancer that has been completely resected and has a 5-year relative survival rate of 95% or more is not included in active multiple/multiple cancers).
  • 2 Infectious disease requiring systemic treatment.
  • 3 Fever of 38.0C or higher at the time of registration.
  • 4 Women who are pregnant, potentially pregnant, within 28 days after childbirth, or breastfeeding.
  • 5 The applicant has a mental illness or psychiatric symptom that interferes with daily life and is judged to be difficult to participate in the study.
  • 6 Receiving continuous systemic administration (oral or intravenous) of steroids or other immunosuppressive drugs.
  • 7 Complicated by uncontrolled diabetes.
  • 8 Complicated by uncontrolled hypertension.
  • 9 Unstable angina (angina pectoris that has developed or exacerbated seizures within the last 3 weeks) or has a history of myocardial infarction within 6 months.
  • 10 Interstitial pneumonia, pulmonary fibrosis, severe emphysema, or more.
  • 11 History of axillary surgery or irradiation
  • 12 Other patients who are judged by the principal investigator or co-investigator to be inappropriate as research subjects

研究者

发起方
Shien Tadahiko

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