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临床试验/NCT03280134
NCT03280134Unknown不适用

CK19 Combined With Contrast-enhanced Ultrasound for Predicting Non-sentinel Lymph Node Status in Early Breast Cancer: a Prospectively Validation Cohort Study of the Predictive Model

Zhejiang Cancer Hospital1 个研究点 分布在 1 个国家目标入组 388 人开始时间: 2018年10月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
388
试验地点
1
主要终点
disease-free survival (DFS)

研究概览

简要总结

In the previous study, the investigator established a predictive model for non-sentinel lymph node involvement in early breast cancer (cT1-2cN0, 1-2 SLNs involvement). To validation the clinical value of the model, the investigator design a prospectively research using the model guiding for further axillary lymph node dissection in SLN-positve early breast cancer.

详细描述

In the previous study, a predictive model for non-sentinel lymph node involvement in early breast cancer (cT1-2cN0, 1-2 SLNs involvement) was established. This model was designed for predicting the status of non-sentinel lymph node in cT1-2cN0 with 1-2 SLNs involvement breast cancer based on peripheral blood CK19 and contrast-enhanced ultrasound. The investigator previously tested this model comparing with MSKCC model in a same population and confirmed a result of satisfactory low false-negative rate and high AUC. This model had a potential practise value in clinic applying. For further validation, the research group design the CK19B trial to prospectively using this model in decision strategy of whether receiving ALND in 1-2SLNs+ patients. If the model predictive result is negative, the risk of nSLNs involvement is estimated very low and the patients should be avoid ALND, even radiotherapy no matter the surgery is mastectomy or conserving. If the model result is positive, then further ALND or radiotherapy should be accepted by patients to decrease the risk of local and regional recurrent. A prospectively and conditional grouping method is planned for this cohort study. The primary endpoint is disease-free survival (DFS) in two groups, the second primary endpoint is local recurrent rate (LRR) and overall survival (OS).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • the test group should be in accordance with the pathological diagnosis of breast cancer, the clinical stage of breast cancer (stage cTis, cI, cII and cT3N1M0), the initial treatment to receive surgical treatment. Complete preoperative clinical diagnosis data, including the ipsilateral axillary lymph node CEUS data and peripheral blood sample; The negative-control group should comply with the pathological diagnosis, breast adenosis, fibrocystic lesions, breast cysts and other benign lesions, with complete preoperative clinical data, also including ipsilateral axillary lymph node CEUS data and peripheral blood sample

排除标准

  • metastatic breast cancer, inflammatory breast disease, surgery without lymph node staging
  • pregnancy or lactation
  • patients with hematopoietic system disease or cancer, autoimmune diseases
  • preservation of substandard peripheral blood samples.

研究组 & 干预措施

predictive nSLN-

No Intervention

No further axillary lymph node dissection (ALND)

predictive nSLN+

Active Comparator

axillary lymph node dissection (ALND)

干预措施: axillary lymph node dissection (ALND) (Procedure)

结局指标

主要结局

disease-free survival (DFS)

时间窗: 3-year(mid-term) 5-year

The time from enrollment to the first recurrent or metastasis event

次要结局

  • overal survival (OS)(3-year(mid-term) 5-year)
  • local recurrent rate(3-year(mid-term) 5-year)

研究者

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

YU Xingfei

Dr.

Zhejiang Cancer Hospital

研究点 (1)

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