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Sentinel Lymph Node Procedure in Ipsilateral Invasive Breast Cancer Relapse (FIGARO)

Primary Purpose

Invasive Breast Cancer, Ipsilateral Recurrence, Sentinel Lymph Node Biopsy

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Sentinel LN in breast cancer recurrence
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 Neoplasm Staging, Neoplasm Recurrence, Axillary lymph node dissection, Conservative surgery

Eligibility Criteria

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

Inclusion Criteria:

  1. Patients ≥ 18 years old
  2. Invasive recurrence (ductal, lobular, other), homolateral breast carcinoma
  3. Size of the tumor with ultrasound ≤ 5cm
  4. Initial conservative surgery
  5. Patient who has already received SLND for her initial cancer, regardless of the SLND result
  6. Procedure for the detection of lymph node sentinel by isotopic method +/- colorimetric
  7. Minimum delay of one year between the end of radiotherapy for initial breast carcinoma and the treatment / management of ipsilateral recurrence
  8. Pregnancy test (urinary or blood) negative for premenopausal patients
  9. Information of the patient and obtaining written consent, signed by the patient and the investigator

Exclusion Criteria:

  1. Non-invasive recurrence
  2. History of ipsilateral axillary dissection
  3. History of ipsilateral mastectomy
  4. Patient pN + before surgery
  5. Metastasis
  6. Allergy known to 2 detection products (Blue and radioactive tracer)
  7. Pregnant or lactating woman
  8. Patient protected or under guardianship or unable to give consent
  9. Impossibility of submitting to the medical examination for geographical, social or psychological reasons

Sites / Locations

  • Institut Bergonie
  • CENTRE REGIONAL DE LUTTE CONTRE LE CANCER D'AUVERGNE - centre JEAN PERRIN
  • Centre Georges Francoise Leclerc
  • ICM Val d'Aurelle
  • INSTITUT REGIONAL DU CANCER MONTPELLIER - Val D'Aurelle
  • Centre Antoine Lacassagne
  • Ico Nantes
  • Institut Curie
  • IUCT-O Institut Claudius Regaud

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Sentinel LN in breast cancer recurrence

Arm Description

Patients with a biopsy assessing an ipsilateral breast tumor recurrence, and a diagnosis of invasive carcinoma after a previous diagnosis of breast cancer that has been treated by breast conservative surgery at least one year before. Before the SLNB procedure, each patient will have a lymphoscintigraphy to evaluate axillary and extra axillary lymphatic mapping. Patients will be operated by breast conservative surgery (BCS) or mastectomy. Each patient will have a second SLND followed by a systematic complete ALND.

Outcomes

Primary Outcome Measures

False-negative rate in patients with a second SLNB procedure for IBTR
Ratio of the number of cases with detection of negative sentinel axillary lymph node but with at least one metastatic lymph node in the axillary dissection on the total number of patients with at least one detected a sentinel axillary node and at least one metastatic lymph node, either in a sentinel axillary lymph node or in complete ALND

Secondary Outcome Measures

Detection rate
Ratio of the number of patients injected, technetium +/- blue, in which at least one sentinel axillary lymph node was detected intraoperative on the total number of patients injected
lymph node involvement
% of lymph node involvement
patient requiring consolidation radiotherapy
% of patient requiring consolidation radiotherapy on axillary and extra-axillary lymph node sites
% of extra-axillary positivity by lymphoscintigraphy
Lymphoscintigraphy will be performed within 24 hours before surgery
Recurrence Free Survival (RFS)
Time until recurrence

Full Information

First Posted
August 7, 2018
Last Updated
April 19, 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
NCT03630653
Brief Title
Sentinel Lymph Node Procedure in Ipsilateral Invasive Breast Cancer Relapse
Acronym
FIGARO
Official Title
Feasibility and Accuracy of Lymph-node (LN) Restaging by Sentinel LN Procedure and Axillary LN Dissection in Ipsilateral Invasive Breast Cancer Relapse
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Terminated
Why Stopped
The study was stopped prematurely due to insufficient recruitment
Study Start Date
May 29, 2018 (Actual)
Primary Completion Date
December 3, 2020 (Actual)
Study Completion Date
December 3, 2020 (Actual)

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 biopsy (SLNB) has become the standard procedure for staging of patients with clinically node-negative breast cancer. Breast-conserving surgery (BCS) has also been a standard treatment for patients with early breast cancer. However, approximately 10% of patients with BCS develop ipsilateral breast tumor recurrence (IBTR), and mastectomy or resection of the recurrent tumor is generally performed. There are no specific guidelines available regarding staging and treatment of the regional lymph nodes. However, the reported risk of axillary lymph node metastasis among patients with local recurrence after breast surgery and a previous negative sentinel node biopsy of 26 % is too high to be ignored. Moreover, evaluation of the regional lymph node basins might be helpful to decide on the indication for adjuvant radiotherapy and systemic treatment. For these reasons it seems sensible to perform a regional lymph node staging procedure in patients with locally recurrent breast cancer. In general practice, this would mean that patients with recurrent breast cancer and a previous negative sentinel node biopsy would receive an axillary lymph node dissection (ALND) and that patients with a previous ALND would receive no additional axillary staging. Lymphatic drainage after previous breast surgery and/or radiotherapy would be altered and it remains questionable whether SLNB at the time of surgery for IBTR (second SLNB) is technically feasible and ALND can safely be omitted. In this study, investigators propose for all patients the realization of SLNB procedure and systematically ALND whatever the results of SLNB analysis, only on patients previously treated with breast conservative surgery. The aim of this study is to evaluate on a homogeneous prospective multicentric cohort of patients the feasibility and the accuracy of a second SLNB procedure for IBTR.
Detailed Description
FIGARO is a prospective multicentre phase-2 study that aims to evaluate technical feasibility and validity of performing second sentinel lymph node dissection (SLND) in patients with IBTR . To be included, patients must have a biopsy assessing an ipsilateral breast tumor recurrence, and a diagnosis of invasive carcinoma after a previous diagnosis of breast cancer that has been treated by breast conservative surgery at least one year before (time between the end of the previous radiotherapy and the diagnosis of recurrence). At time of recurrence, the patients must be evaluated by X-ray mammography and ultrasonography examination of breast and axilla, and a full general assessment to eliminate distant metastasis. Local recurrences will be operated by breast conservative surgery (BCS) or mastectomy. The decision between BCS and mastectomy will be carefully considered, in accordance with patient preference and other clinical features such as tumor location, tumor size, and breast size taken into account. Each patient will have a second SLNB followed by a systematic complete ALND. Before the SLNB procedure, each patient will have a lymphoscintigraphy to evaluate axillary and extra axillary lymphatic mapping. Lymphoscintigraphy will be performed according to previously reported standard techniques. At 2-20 h after lymphoscintigraphy, SLNB will be performed with or without a blue dye associated injection. An intraoperative gamma ray detection probe will be used during surgery to confirm locations of the sentinel nodes and to facilitate their removal. All sentinel nodes will be removed and sent for histopathologic examination according to previously described standard techniques. A complete ALND (Berg's stage I and II) will be realized and the nodes will be sent for standard histopathologic examination. Further systemic adjuvant therapies will be chosen in a multidisciplinary approach considering prognostic and predictive indicators. All the patients will be followed up for 5 years at 12-month intervals after the second surgery and undergo annual mammography with or without ultrasonography.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Invasive Breast Cancer, Ipsilateral Recurrence, Sentinel Lymph Node Biopsy
Keywords
Neoplasm Staging, Neoplasm Recurrence, Axillary lymph node dissection, Conservative surgery

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Sentinel LN in breast cancer recurrence
Arm Type
Experimental
Arm Description
Patients with a biopsy assessing an ipsilateral breast tumor recurrence, and a diagnosis of invasive carcinoma after a previous diagnosis of breast cancer that has been treated by breast conservative surgery at least one year before. Before the SLNB procedure, each patient will have a lymphoscintigraphy to evaluate axillary and extra axillary lymphatic mapping. Patients will be operated by breast conservative surgery (BCS) or mastectomy. Each patient will have a second SLND followed by a systematic complete ALND.
Intervention Type
Procedure
Intervention Name(s)
Sentinel LN in breast cancer recurrence
Intervention Description
Sentinel Lymph-Node (LN) procedure and Axillary LN dissection ; Mastectomy or breast conservative surgery
Primary Outcome Measure Information:
Title
False-negative rate in patients with a second SLNB procedure for IBTR
Description
Ratio of the number of cases with detection of negative sentinel axillary lymph node but with at least one metastatic lymph node in the axillary dissection on the total number of patients with at least one detected a sentinel axillary node and at least one metastatic lymph node, either in a sentinel axillary lymph node or in complete ALND
Time Frame
30 days post-surgery
Secondary Outcome Measure Information:
Title
Detection rate
Description
Ratio of the number of patients injected, technetium +/- blue, in which at least one sentinel axillary lymph node was detected intraoperative on the total number of patients injected
Time Frame
1 to 2 hours post-surgery
Title
lymph node involvement
Description
% of lymph node involvement
Time Frame
30 days post-surgery
Title
patient requiring consolidation radiotherapy
Description
% of patient requiring consolidation radiotherapy on axillary and extra-axillary lymph node sites
Time Frame
30 days post-surgery
Title
% of extra-axillary positivity by lymphoscintigraphy
Description
Lymphoscintigraphy will be performed within 24 hours before surgery
Time Frame
Within 24 hours before surgery
Title
Recurrence Free Survival (RFS)
Description
Time until recurrence
Time Frame
Up to 5 years post-surgery

10. Eligibility

Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients ≥ 18 years old Invasive recurrence (ductal, lobular, other), homolateral breast carcinoma Size of the tumor with ultrasound ≤ 5cm Initial conservative surgery Patient who has already received SLND for her initial cancer, regardless of the SLND result Procedure for the detection of lymph node sentinel by isotopic method +/- colorimetric Minimum delay of one year between the end of radiotherapy for initial breast carcinoma and the treatment / management of ipsilateral recurrence Pregnancy test (urinary or blood) negative for premenopausal patients Information of the patient and obtaining written consent, signed by the patient and the investigator Exclusion Criteria: Non-invasive recurrence History of ipsilateral axillary dissection History of ipsilateral mastectomy Patient pN + before surgery Metastasis Allergy known to 2 detection products (Blue and radioactive tracer) Pregnant or lactating woman Patient protected or under guardianship or unable to give consent Impossibility of submitting to the medical examination for geographical, social or psychological reasons
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
VIRGINIE BORDES, MD
Organizational Affiliation
ICO
Official's Role
Study Director
Facility Information:
Facility Name
Institut Bergonie
City
Bordeaux
ZIP/Postal Code
33076
Country
France
Facility Name
CENTRE REGIONAL DE LUTTE CONTRE LE CANCER D'AUVERGNE - centre JEAN PERRIN
City
Clermont-ferrand
ZIP/Postal Code
63011
Country
France
Facility Name
Centre Georges Francoise Leclerc
City
Dijon
ZIP/Postal Code
21079
Country
France
Facility Name
ICM Val d'Aurelle
City
Montpellier
ZIP/Postal Code
34298
Country
France
Facility Name
INSTITUT REGIONAL DU CANCER MONTPELLIER - Val D'Aurelle
City
Montpellier
ZIP/Postal Code
34298
Country
France
Facility Name
Centre Antoine Lacassagne
City
Nice
ZIP/Postal Code
06189
Country
France
Facility Name
Ico Nantes
City
Saint Herblain
ZIP/Postal Code
44805
Country
France
Facility Name
Institut Curie
City
Saint-Cloud
ZIP/Postal Code
92210
Country
France
Facility Name
IUCT-O Institut Claudius Regaud
City
Toulouse
ZIP/Postal Code
31059
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Sentinel Lymph Node Procedure in Ipsilateral Invasive Breast Cancer Relapse

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