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Spots Global Cancer Trial Database for Sentinel Lymph Node After Neoadjuvant Chemotherapy in Breast Carcinoma

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Trial Identification

Brief Title: Sentinel Lymph Node After Neoadjuvant Chemotherapy in Breast Carcinoma

Official Title: Sentinel Lymph Node After Neoadjuvant Chemotherapy in Breast Carcinoma

Study ID: NCT03630913

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

ICO - Site ANGERS, Angers, , France

Institut Bergonié, Bordeaux, , France

CHU Brest, Brest, , France

Centre Jean Perrin, Clermont-Ferrand, , France

Centre Georges Francoise Leclerc, Dijon, , France

Oscar Lambret, Lille, , France

Centre Léon Bérard, Lyon, , France

Institut Paoli Calmettes, Marseille, , France

Institut de Cancérologie de Montpellier, Montpellier, , France

APHP - Pitié Salpétrière, Paris, , France

Hôpital St JOSEPH, Paris, , France

Anne-Sophie Georges BATS, Paris, , France

Centre Jean Godinot, Reims, , France

Céline RENAUDEAU, Saint Herblain, , France

CURIE, Saint-Cloud, , France

CHP St GREGOIRE, Saint-Grégoire, , France

IUCT-O, Toulouse, , France

Institut de Cancérlogie de Lorraine, Vandœuvre-lès-Nancy, , France

Contact Details

Name: JEAN-MARC CLASSE, MD

Affiliation: ICO NANTES

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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