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Contrast-enhanced Ultrasonography Combined With Blue Dye as Dual-tracer for Sentinel Lymph Node Biopsy (Asclepius)

Primary Purpose

Breast Neoplasms, Neoadjuvant Therapy, Sentinel Lymph Node Biopsy

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
CEUS
blue dye
Sponsored by
First Affiliated Hospital, Sun Yat-Sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Breast Neoplasms focused on measuring contrast enhanced ultrasonography

Eligibility Criteria

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

Inclusion Criteria:

  • ≥18 years old female;
  • ECOG:0 - 1;
  • Biopsy confirmed invasive breast cancer;
  • cT1-4N0-3;
  • Signed informed consent.

Exclusion Criteria:

  • Inflammatory breast cancer;
  • Received ipsilateral axillary surgery previously;
  • During pregnancy.

Sites / Locations

  • The first affiliated hospital of Sun Yat-Sen university

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

CEUS+blue dye

Arm Description

The included patients will accept essential tests and CEUS before and after neoadjuvant chemotherapy to evaluate axillary lymph nodes status. When patients finish neoadjuvant therapy, SLNB with or without axillary lymph node dissection will be performed using CEUS lymphatic mapping to mark SLN on the skin combined with blue dye.

Outcomes

Primary Outcome Measures

False negative rate
The false negative rate (FNR) of sentinel lymph node biopsy using dual-tracer with CEUS and blue dye after neoadjuvant chemotherapy in invasive breast cancer patients. The FNR is calculated as the number of false negative cases divided by the number of false negative plus true positive cases and then multiplied by 100%.

Secondary Outcome Measures

The detective rate of sentinel lymph node biopsy
The detective rate of SLNB after neoadjuvant therapy when using blue dye and CEUS lymphatic mapping as dual tracer. The detective rate is calculated as the number of patients in whom SLN can be detected during SLNB divided by the number of patients with the treatment of SLNB and then multiplied by 100%.
The average numbers of sentinel lymph node
The average numbers of sentinel lymph node is calculated as the number of all SLNs detected during SLNB divided by the number of patients received SLNB and then multiplied by 100%.
The accuracy of CEUS in evaluation of axillary lymph nodes in breast cancer
The accuracy of CEUS in evaluation of axillary lymph nodes in breast cancer patients before and after neoadjuvant therapy. The accuracy rate is calculated as the number of true positive plus true negative cases divided by the number of patients then multiplied by 100%.

Full Information

First Posted
May 31, 2021
Last Updated
June 18, 2021
Sponsor
First Affiliated Hospital, Sun Yat-Sen University
Collaborators
The Seventh Affiliated Hospital of Sun Yat-sen University, Affiliated Hospital of Guangdong Medical University, First Affiliated Hospital of Shantou University Medical College
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1. Study Identification

Unique Protocol Identification Number
NCT04932460
Brief Title
Contrast-enhanced Ultrasonography Combined With Blue Dye as Dual-tracer for Sentinel Lymph Node Biopsy
Acronym
Asclepius
Official Title
A Prospective Multi-center Study: Contrast-enhanced Ultrasonography Combined With Blue Dye as Dual-tracer for Sentinel Lymph Node Biopsy After Neoadjuvant Therapy in Breast Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Unknown status
Study Start Date
June 15, 2021 (Anticipated)
Primary Completion Date
July 15, 2023 (Anticipated)
Study Completion Date
August 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
First Affiliated Hospital, Sun Yat-Sen University
Collaborators
The Seventh Affiliated Hospital of Sun Yat-sen University, Affiliated Hospital of Guangdong Medical University, First Affiliated Hospital of Shantou University Medical College

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
False negative rate (FNR) in patients who has accepted neoadjuvant therapy is high. Blue dye and radioisotope as dual-tracer can decrease FNR. Several large clinical trials showed that using dual trace with blue dye and radioisotope can reduce the FNR to less than 10%. But radioisotope is still not approved in China and can cause radiocontamination. A novel dual-tracer which can decrease the FNR in patients after neoadjuvant therapy is urged to be explored. Contrast enhanced ultrasonography (CEUS) can make the lymphatic drainage path and sentinel lymph nodes visible. Retrospective studies found that CEUS can locate SLN precisely. So this clinical trial aim to evaluate FNR, detective rate and numbers of SLN by using CEUS combined with blue dye as dual-tracer in sentinel lymph node biopsy in breast cancer patients after neoadjuvant therapy and the accuracy of CEUS for the diagnosis of lymph node metastasis before and after neoadjuvant therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Neoplasms, Neoadjuvant Therapy, Sentinel Lymph Node Biopsy
Keywords
contrast enhanced ultrasonography

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
350 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CEUS+blue dye
Arm Type
Experimental
Arm Description
The included patients will accept essential tests and CEUS before and after neoadjuvant chemotherapy to evaluate axillary lymph nodes status. When patients finish neoadjuvant therapy, SLNB with or without axillary lymph node dissection will be performed using CEUS lymphatic mapping to mark SLN on the skin combined with blue dye.
Intervention Type
Procedure
Intervention Name(s)
CEUS
Intervention Description
CEUS is performed before neoadjuvant treatment and surgery to evaluate the status of axillary lymph node and locate the sentinel lymph node.
Intervention Type
Procedure
Intervention Name(s)
blue dye
Intervention Description
Before operation, blue dye is injected for sentinel lymph node mapping.
Primary Outcome Measure Information:
Title
False negative rate
Description
The false negative rate (FNR) of sentinel lymph node biopsy using dual-tracer with CEUS and blue dye after neoadjuvant chemotherapy in invasive breast cancer patients. The FNR is calculated as the number of false negative cases divided by the number of false negative plus true positive cases and then multiplied by 100%.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
The detective rate of sentinel lymph node biopsy
Description
The detective rate of SLNB after neoadjuvant therapy when using blue dye and CEUS lymphatic mapping as dual tracer. The detective rate is calculated as the number of patients in whom SLN can be detected during SLNB divided by the number of patients with the treatment of SLNB and then multiplied by 100%.
Time Frame
6 months
Title
The average numbers of sentinel lymph node
Description
The average numbers of sentinel lymph node is calculated as the number of all SLNs detected during SLNB divided by the number of patients received SLNB and then multiplied by 100%.
Time Frame
6 months
Title
The accuracy of CEUS in evaluation of axillary lymph nodes in breast cancer
Description
The accuracy of CEUS in evaluation of axillary lymph nodes in breast cancer patients before and after neoadjuvant therapy. The accuracy rate is calculated as the number of true positive plus true negative cases divided by the number of patients then multiplied by 100%.
Time Frame
6 months

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥18 years old female; ECOG:0 - 1; Biopsy confirmed invasive breast cancer; cT1-4N0-3; Signed informed consent. Exclusion Criteria: Inflammatory breast cancer; Received ipsilateral axillary surgery previously; During pregnancy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ying Lin
Phone
13076873871
Email
linying3@mail.sysu.edu.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Zhen Shan
Phone
18565396593
Email
szsysu@126.com
Facility Information:
Facility Name
The first affiliated hospital of Sun Yat-Sen university
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510000
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
23683750
Citation
Kuehn T, Bauerfeind I, Fehm T, Fleige B, Hausschild M, Helms G, Lebeau A, Liedtke C, von Minckwitz G, Nekljudova V, Schmatloch S, Schrenk P, Staebler A, Untch M. Sentinel-lymph-node biopsy in patients with breast cancer before and after neoadjuvant chemotherapy (SENTINA): a prospective, multicentre cohort study. Lancet Oncol. 2013 Jun;14(7):609-18. doi: 10.1016/S1470-2045(13)70166-9. Epub 2013 May 15.
Results Reference
result
PubMed Identifier
25452445
Citation
Boileau JF, Poirier B, Basik M, Holloway CM, Gaboury L, Sideris L, Meterissian S, Arnaout A, Brackstone M, McCready DR, Karp SE, Trop I, Lisbona A, Wright FC, Younan RJ, Provencher L, Patocskai E, Omeroglu A, Robidoux A. Sentinel node biopsy after neoadjuvant chemotherapy in biopsy-proven node-positive breast cancer: the SN FNAC study. J Clin Oncol. 2015 Jan 20;33(3):258-64. doi: 10.1200/JCO.2014.55.7827. Epub 2014 Dec 1.
Results Reference
result

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Contrast-enhanced Ultrasonography Combined With Blue Dye as Dual-tracer for Sentinel Lymph Node Biopsy

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