search
Back to results

A Prospective Validation Cohort Study of a Prediction System on nSLN Metastasis in Early Breast Cancer

Primary Purpose

Lymph Node Metastases, Breast Cancer, Predictive Cancer Model

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
axillary lymph node dissection (ALND)
Sponsored by
Zhejiang Cancer Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lymph Node Metastases focused on measuring non-sentinel lymph node, breast cancer, prediction, CK19, contrast-enhanced ultrasound

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

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

Exclusion Criteria:

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

Sites / Locations

  • Zhejiang Cancer HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

predictive nSLN-

predictive nSLN+

Arm Description

No further axillary lymph node dissection (ALND)

axillary lymph node dissection (ALND)

Outcomes

Primary Outcome Measures

disease-free survival (DFS)
The time from enrollment to the first recurrent or metastasis event

Secondary Outcome Measures

local recurrent rate
The time from enrollment to the first time of local recurrent event (lymph drainage area recurrence)
overal survival (OS)
The time from enrollment to death for any reason

Full Information

First Posted
September 9, 2017
Last Updated
June 2, 2019
Sponsor
Zhejiang Cancer Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT03280134
Brief Title
A Prospective Validation Cohort Study of a Prediction System on nSLN Metastasis in Early Breast Cancer
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Unknown status
Study Start Date
October 15, 2018 (Actual)
Primary Completion Date
December 2019 (Anticipated)
Study Completion Date
June 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zhejiang Cancer Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
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.
Detailed Description
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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymph Node Metastases, Breast Cancer, Predictive Cancer Model
Keywords
non-sentinel lymph node, breast cancer, prediction, CK19, contrast-enhanced ultrasound

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This study based on prospective cohort method and concerning on the two groups (whether ALND or not) by predictive model nSLN results.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
388 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
predictive nSLN-
Arm Type
No Intervention
Arm Description
No further axillary lymph node dissection (ALND)
Arm Title
predictive nSLN+
Arm Type
Active Comparator
Arm Description
axillary lymph node dissection (ALND)
Intervention Type
Procedure
Intervention Name(s)
axillary lymph node dissection (ALND)
Intervention Description
If the patients had predictive nSLN+, need further axillary lymph node dissection.
Primary Outcome Measure Information:
Title
disease-free survival (DFS)
Description
The time from enrollment to the first recurrent or metastasis event
Time Frame
3-year(mid-term) 5-year
Secondary Outcome Measure Information:
Title
local recurrent rate
Description
The time from enrollment to the first time of local recurrent event (lymph drainage area recurrence)
Time Frame
3-year(mid-term) 5-year
Title
overal survival (OS)
Description
The time from enrollment to death for any reason
Time Frame
3-year(mid-term) 5-year

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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 Exclusion Criteria: 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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
XF YU, M.D.
Phone
+8657188122001
Email
yuxf1177@zjcc.org.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
XF YU, M.D.
Organizational Affiliation
Zhejiang Cancer Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Zhejiang Cancer Hospital
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310022
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xing-Fei YU, MD.
Email
yhjzlyy@163.com
First Name & Middle Initial & Last Name & Degree
Xing-Fei YU, MD.

12. IPD Sharing Statement

Citations:
PubMed Identifier
31659631
Citation
Qiao E, Yu X, Zhou L, Wang C, Yang C, Yu Y, Chen D, Huang J, Yang H. A Prospective Validation Cohort Study of a Prediction Model on Non-sentinel Lymph Node Involvement in Early Breast Cancer. Ann Surg Oncol. 2020 May;27(5):1653-1658. doi: 10.1245/s10434-019-07980-x. Epub 2019 Oct 28.
Results Reference
derived

Learn more about this trial

A Prospective Validation Cohort Study of a Prediction System on nSLN Metastasis in Early Breast Cancer

We'll reach out to this number within 24 hrs