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Sentinel Lymph Node After Neoadjuvant Chemotherapy in Breast Carcinoma (GANEA3)

Primary Purpose

Invasive Breast Cancer, Axillary Metastases

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Tagged axillary metastatic node
Sponsored by
Institut Cancerologie de l'Ouest
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Invasive Breast Cancer focused on measuring Neoadjuvant chemotherapy, Sentinel lymph node, Axillary lymphadenectomy, Tagged axillary metastatic node

Eligibility Criteria

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

Inclusion Criteria:

  1. Patients ≥ 18 years old
  2. Initial diagnosis of operable invasive breast carcinoma
  3. Histologically proven axillary metastasis (cytology or biopsy) before NAC
  4. Patient included in a therapeutic approach of neoadjuvant chemotherapy
  5. Procedure for the detection of sentinel lymph node by isotopic method +/- colorimetric
  6. Information of the patient and obtaining written consent, signed by the patient and the investigator
  7. Affiliated patient or beneficiary of the social security

Exclusion Criteria:

  1. pT4d (inflammatory breast cancer)
  2. Metastatic breast cancer
  3. Any prior chemotherapy for contralateral breast cancer
  4. Local relapse of breast cancer
  5. Axillary metastasis not histologically proven before NAC
  6. Allergy known to the 2 detection products (Blue and radioactive tracer)
  7. Pregnant or lactating woman
  8. Neo Adjuvant chemotherapy contraindicated
  9. Patient protected or under guardianship or unable to give consent
  10. Impossibility of submitting to the medical examination for geographical, social or psychological

Sites / Locations

  • ICO - Site ANGERS
  • Institut Bergonié
  • CHU Brest
  • Centre Jean PerrinRecruiting
  • Centre Georges Francoise LeclercRecruiting
  • Oscar Lambret
  • Centre Léon BérardRecruiting
  • Institut Paoli CalmettesRecruiting
  • Institut de Cancérologie de MontpellierRecruiting
  • APHP - Pitié Salpétrière
  • Hôpital St JOSEPH
  • Anne-Sophie Georges BATS
  • Centre Jean Godinot
  • Céline RENAUDEAURecruiting
  • CURIERecruiting
  • CHP St GREGOIRE
  • IUCT-O
  • Institut de Cancérlogie de LorraineRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Tagged axillary metastatic node

Arm Description

Patients undergo axillary sonography assessment routinely performed to seek suspicious nodes. A cytological examination (biopsy is optional) of the suspicious node is performed. The involved node is then tagged with a metal clip under sonography. Then, patients receive NAC before surgery. Breast surgery (conservative or radical) and axillary surgery are performed during the same procedure, 4 to 6 weeks after completion of NAC.

Outcomes

Primary Outcome Measures

False negative rate
number of cases of false prediction of absence of lymph node involvement to the total number of cases with metastatic lymph node. The rate of FN will be calculated for the involved lymph node tagged with the metal clip, the sentinel node, and the both

Secondary Outcome Measures

Identification rate of involved lymph node tagged
number of cases where the tagged lymph node with a metal clip node is identified during axillary surgery and analyzed in pathology on the total number of procedures
Resection rate of involved lymph node tagged
number of cases where the tagged lymph node is resected during axillary surgery and analyzed in pathology on the total number of procedures
Complication rate
number of complications related to the axillary lymph node tagging procedure on the total number of procedures

Full Information

First Posted
August 10, 2018
Last Updated
April 21, 2022
Sponsor
Institut Cancerologie de l'Ouest
Collaborators
Direction Générale de l'Offre de Soins
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1. Study Identification

Unique Protocol Identification Number
NCT03630913
Brief Title
Sentinel Lymph Node After Neoadjuvant Chemotherapy in Breast Carcinoma
Acronym
GANEA3
Official Title
Sentinel Lymph Node After Neoadjuvant Chemotherapy in Breast Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 8, 2019 (Actual)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
October 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut Cancerologie de l'Ouest
Collaborators
Direction Générale de l'Offre de Soins

4. Oversight

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

5. Study Description

Brief Summary
Sentinel lymph node dissection (SLND) after NAC, aimed to reduce the rate of unnecessary axillary lymphadenectomy, is not a standard of care in case of patient with previously involved node before NAC because of a too high false negative rate (FNR). Clinical consequences of FNR of SLND after NAC are currently unknown. Consequently, contrary to adjuvant setting, a risk of SLND false negative case after NAC is not acceptable. GANEA3 aims to evaluate the results of an innovative multiparametric strategy combining (1) an identification before chemotherapy of a lymph node involvement using a metal clip and then its analysis after treatment, (2) the analysis of sentinel lymph node (SLN) after NAC, and (3) analysis of biological parameters of breast tumor before and after NAC, to predict axillary status after NAC. This will identify patients with initial lymph node involvement who could benefit from SLN after NAC without additional axillary dissection with a very low FNR (≤1%). The most "pathological" metastatic lymph node will be identified with a metal clip under ultrasound. They will then receive a NAC before breast and axillary surgery. An assessment of the NAC response at the breast and axillary will be performed by imagery. Then, all patients undergo the resection of the tagged axillary node with the metal clip, SLN detection and biopsy and a complementary axillary lymphadenectomy.
Detailed Description
GANEA3 is a prospective multicenter diagnostic study assessing the benefit of targeting initial involved node in complement to SLND and breast tumor characteristics to predict axillary status after NAC. The diagnostic performances of this strategy will be primarily assessed by the decrease of the FNR with the combined strategy compared to SLND alone. The primary objective is to evaluate the interest of identifying, before NAC, the initial involved lymph node to improve the prediction of axillary status after NAC. The main secondary objectives are : To assess the feasibility, at the time of the surgery, of the identification and resection of the initially involved lymph node, tagged with the metal clip before NAC ; To evaluate the complications related to the setting up of the metal clip for the identification of a lymph node metastatic ; To evaluate the interest and impact of immunohistochemical analysis of tagged lymph node and SLN ; Patients treated for a large early breast cancer (BC) needing NAC undergo axillary sonography assessment routinely performed to seek suspicious nodes. When several suspicious nodes are found only the worst is chosen. A fine needle aspiration is performed to allow cytological examination (biopsy is optional) of the suspicious node. In case of proven axillary involvement, the patient is informed about GANEA 3 study in order to be included. At this step the patient must accept the study and sign the consent form. The involved node is then tagged (with a metal clip) under sonography. In case of multiple suspicious nodes, the radiologist must choose the worst node in order to tag only one involved node. Then, then patients will perform their chemotherapy. The choice of NAC regimen is let at the discretion of each participating team. After NAC, breast tumor size and axillary assessment are performed. Breast and axillary surgery are performed during the same procedure, 4 to 6 weeks after completion of NAC. Breast surgery can be conservative or radical. All patients undergo the resection of the tagged axillary node, SLN biopsy and a complementary axillary lymphadenectomy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Invasive Breast Cancer, Axillary Metastases
Keywords
Neoadjuvant chemotherapy, Sentinel lymph node, Axillary lymphadenectomy, Tagged axillary metastatic node

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Tagged axillary metastatic node
Arm Type
Experimental
Arm Description
Patients undergo axillary sonography assessment routinely performed to seek suspicious nodes. A cytological examination (biopsy is optional) of the suspicious node is performed. The involved node is then tagged with a metal clip under sonography. Then, patients receive NAC before surgery. Breast surgery (conservative or radical) and axillary surgery are performed during the same procedure, 4 to 6 weeks after completion of NAC.
Intervention Type
Procedure
Intervention Name(s)
Tagged axillary metastatic node
Intervention Description
First, initially metastatic lymph node is tagged with a metal clip under sonography. Then, patients receive NAC before surgery. Breast surgery (conservative or radical) and axillary surgery are performed during the same procedure, 4 to 6 weeks after completion of NAC. SLN isotope detection is performed with or without blue dye. All patients undergo the resection of the tagged axillary node, SLN biopsy and a complementary axillary lymphadenectomy.
Primary Outcome Measure Information:
Title
False negative rate
Description
number of cases of false prediction of absence of lymph node involvement to the total number of cases with metastatic lymph node. The rate of FN will be calculated for the involved lymph node tagged with the metal clip, the sentinel node, and the both
Time Frame
30 days after surgery
Secondary Outcome Measure Information:
Title
Identification rate of involved lymph node tagged
Description
number of cases where the tagged lymph node with a metal clip node is identified during axillary surgery and analyzed in pathology on the total number of procedures
Time Frame
30 days after surgery
Title
Resection rate of involved lymph node tagged
Description
number of cases where the tagged lymph node is resected during axillary surgery and analyzed in pathology on the total number of procedures
Time Frame
30 days after surgery
Title
Complication rate
Description
number of complications related to the axillary lymph node tagging procedure on the total number of procedures
Time Frame
30 days after surgery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients ≥ 18 years old Initial diagnosis of operable invasive breast carcinoma Histologically proven axillary metastasis (cytology or biopsy) before NAC Patient included in a therapeutic approach of neoadjuvant chemotherapy Procedure for the detection of sentinel lymph node by isotopic method +/- colorimetric Information of the patient and obtaining written consent, signed by the patient and the investigator Affiliated patient or beneficiary of the social security Exclusion Criteria: pT4d (inflammatory breast cancer) Metastatic breast cancer Any prior chemotherapy for contralateral breast cancer Local relapse of breast cancer Axillary metastasis not histologically proven before NAC Allergy known to the 2 detection products (Blue and radioactive tracer) Pregnant or lactating woman Neo Adjuvant chemotherapy contraindicated Patient protected or under guardianship or unable to give consent Impossibility of submitting to the medical examination for geographical, social or psychological
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
JEAN-MARC CLASSE, MD
Phone
+33240679910
Email
Jean-Marc.Classe@ico.unicancer.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
JEAN-MARC CLASSE, MD
Organizational Affiliation
ICO NANTES
Official's Role
Study Director
Facility Information:
Facility Name
ICO - Site ANGERS
City
Angers
ZIP/Postal Code
49055
Country
France
Individual Site Status
Suspended
Facility Name
Institut Bergonié
City
Bordeaux
ZIP/Postal Code
33076
Country
France
Individual Site Status
Suspended
Facility Name
CHU Brest
City
Brest
ZIP/Postal Code
29609
Country
France
Individual Site Status
Suspended
Facility Name
Centre Jean Perrin
City
Clermont-Ferrand
ZIP/Postal Code
63011
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pierre GUIMBERGUES, MD
Email
pierre.gimbergues@cjp.fr
First Name & Middle Initial & Last Name & Degree
Pierre GIMBERGUES, MD
Facility Name
Centre Georges Francoise Leclerc
City
Dijon
ZIP/Postal Code
21079
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Clémentine JANKOWSKI, MD
Email
cjankowski@cgfl.fr
First Name & Middle Initial & Last Name & Degree
Clémentine JANKOWSKI, MD
Facility Name
Oscar Lambret
City
Lille
Country
France
Individual Site Status
Suspended
Facility Name
Centre Léon Bérard
City
Lyon
ZIP/Postal Code
69373
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Centre L Bérard, MD
Email
christelle.faure@lyon.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Christelle FAURE, MD
Facility Name
Institut Paoli Calmettes
City
Marseille
ZIP/Postal Code
13009
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Monique COHEN, MD
Email
cohenm@ipc.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Monique COHEN, MD
Facility Name
Institut de Cancérologie de Montpellier
City
Montpellier
ZIP/Postal Code
34298
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
GUTOWSKI Marian, MD
Email
marian.gutowski@icm.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Marian GUTOWSKI, MD
Facility Name
APHP - Pitié Salpétrière
City
Paris
ZIP/Postal Code
75013
Country
France
Individual Site Status
Suspended
Facility Name
Hôpital St JOSEPH
City
Paris
ZIP/Postal Code
75014
Country
France
Individual Site Status
Suspended
Facility Name
Anne-Sophie Georges BATS
City
Paris
ZIP/Postal Code
75908
Country
France
Individual Site Status
Suspended
Facility Name
Centre Jean Godinot
City
Reims
ZIP/Postal Code
51726
Country
France
Individual Site Status
Suspended
Facility Name
Céline RENAUDEAU
City
Saint Herblain
ZIP/Postal Code
44805
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Céline RENAUDEAU, MD
Phone
+33240679900
Email
celine.renaudeau@ico.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Céline RENAUDEAU, MD
Facility Name
CURIE
City
Saint-Cloud
ZIP/Postal Code
92210
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eugénie GUILLOT
Email
eugenie.guillot@curie.fr
First Name & Middle Initial & Last Name & Degree
Eugénie GUILLOT, MD
Facility Name
CHP St GREGOIRE
City
Saint-Grégoire
ZIP/Postal Code
35760
Country
France
Individual Site Status
Suspended
Facility Name
IUCT-O
City
Toulouse
ZIP/Postal Code
31059
Country
France
Individual Site Status
Suspended
Facility Name
Institut de Cancérlogie de Lorraine
City
Vandœuvre-lès-Nancy
ZIP/Postal Code
54511
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Philippe RAUCH, MD
Email
p.rauch@nancy.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Philippe RAUCH, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
31833973
Citation
Ditsch N, Rubio IT, Gasparri ML, de Boniface J, Kuehn T. Breast and axillary surgery in malignant breast disease: a review focused on literature of 2018 and 2019. Curr Opin Obstet Gynecol. 2020 Feb;32(1):91-99. doi: 10.1097/GCO.0000000000000593.
Results Reference
derived

Learn more about this trial

Sentinel Lymph Node After Neoadjuvant Chemotherapy in Breast Carcinoma

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