Sentinel Lymph Node After Neoadjuvant Chemotherapy in Breast Carcinoma

Last updated: April 21, 2022
Sponsor: Institut Cancerologie de l'Ouest
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT03630913
ICO-N-2018-03
  • Ages > 18
  • Female

Study 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.

Eligibility Criteria

Inclusion

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 andthe investigator
  7. Affiliated patient or beneficiary of the social security

Exclusion

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 orpsychological

Study Design

Total Participants: 385
Study Start date:
January 08, 2019
Estimated Completion Date:
October 31, 2023

Study 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.

Connect with a study center

  • ICO - Site ANGERS

    Angers, 49055
    France

    Suspended

  • Polyclinique Urbain

    Avignon, 84000
    France

    Site Not Available

  • Institut Bergonié

    Bordeaux, 33076
    France

    Suspended

  • CHU Brest

    Brest, 29609
    France

    Suspended

  • Centre Jean Perrin

    Clermont-Ferrand, 63011
    France

    Active - Recruiting

  • Centre Georges Francoise Leclerc

    Dijon, 21079
    France

    Active - Recruiting

  • Oscar Lambret

    Lille,
    France

    Suspended

  • Centre Léon Bérard

    Lyon, 69373
    France

    Active - Recruiting

  • Institut Paoli Calmettes

    Marseille, 13009
    France

    Active - Recruiting

  • Institut de Cancérologie de Montpellier

    Montpellier, 34298
    France

    Active - Recruiting

  • Centre Antoine Lacassagne

    Nice, 06189
    France

    Site Not Available

  • APHP - Pitié Salpétrière

    Paris, 75013
    France

    Suspended

  • Anne-Sophie Georges BATS

    Paris, 75908
    France

    Suspended

  • Hôpital St JOSEPH

    Paris, 75014
    France

    Suspended

  • Centre Jean Godinot

    Reims, 51726
    France

    Suspended

  • Céline RENAUDEAU

    Saint Herblain, 44805
    France

    Active - Recruiting

  • CURIE

    Saint-Cloud, 92210
    France

    Active - Recruiting

  • CHP St GREGOIRE

    Saint-Grégoire, 35760
    France

    Suspended

  • Centre Paul Strauss

    Strasbourg, 67065
    France

    Site Not Available

  • IUCT-O

    Toulouse, 31059
    France

    Suspended

  • Institut de Cancérlogie de Lorraine

    Vandœuvre-lès-Nancy, 54511
    France

    Active - Recruiting

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