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
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