ARM: Axillary Reverse Mapping in Breast Cancer

Sponsor
Hospital Universitari de Bellvitge (Other)
Overall Status
Recruiting
CT.gov ID
NCT05040685
Collaborator
(none)
30
1
1
18
1.7

Study Details

Study Description

Brief Summary

The axillary mapping reverse (ARM) consists in differentiating the upper limb lymph nodes from the breast ones in order to preserve them and reduce the possibility of lymphedema.

A significant decrease of lymphedema rates in patients who was possible associate ARM technique during the axillary surgery improving the quality of life of these patients. There are different visualisation techniques like fluorescence dye.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Axillary mapping reverse
N/A

Detailed Description

Axillary lymph node dissection (ALND) was the standard therapy until 1990-2000, when the technique was replaced, when possible, by another procedure associated with less morbidity: the sentinel lymph node biopsy (SLNB). However, actually, ALND is still the gold standard in some patients. This procedure is associated with substantial morbidity, like lymphedema, shoulder pain, arm numbness, axillary web syndrome and decreased upper-extremity range of motion (ROM), that severely conditions the quality of life of these patients.

In 2007, the investigators had the first reports about a new surgical technique, the axillary mapping reverse (ARM), that consists in differentiating the upper limb lymph nodes from the breast ones in order to preserve them and reduce the possibility of lymphedema.

The current literature shows a significant decrease of lymphedema rates in patients who was possible associate this technique during the axillary surgery improving the quality of life of these patients. There are different visualisation techniques. With the use of indocyanine green, the visualisation rates in the axilla of ARM lymphatics are from 88%, similar to other techniques. Some advantages of fluorescence dye are that no systemic allergic reactions have been reported and the 'green tattoo' disappears quickly.

HYPHOTESIS The axillary mapping reverse (AMR) is able to identify the lymph nodes responsible for lymphatic drainage of the ipsilateral upper limb (ARM nodes) in breast cancer patients who underwent an axillar lymph node dissection.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
This is a prospective not randomized pilot study to validate the axillary mapping reverse technique by using indocyanine green.This is a prospective not randomized pilot study to validate the axillary mapping reverse technique by using indocyanine green.
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Axillary Reverse Mapping (ARM): Validation of Surgical Tecnique in Breast Cancer Surgery
Actual Study Start Date :
Jun 1, 2021
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Axillary mapping reverse

Application of axillary mapping reverse technique

Procedure: Axillary mapping reverse
At the time of performing the ALND associate the ARM, injecting between 2-5mL of indocyanine green subcutaneously in the ipsilateral upper extremity at the medial inter-muscular and massaged for 5 min. First, identify the ARM nodes by indocyanine green, then perform conventional axillary lymphadenectomy trying to preserve the ARM nodes. And, in a second time, extract ARM nodes for their individualized anatomopathological study.

Outcome Measures

Primary Outcome Measures

  1. Rate of patients who it is possible preserve ARM nodes [1 year]

    Determinate the percentage of patients who is possible preserve the ARM node during ALND

Secondary Outcome Measures

  1. Rate of metastatic ARM [1 year]

    Determinate the percentage of metastatic ARM nodes.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
Patients who will undergo ALND in the treatment of breast cancer:
  • cT4a, cT4c and cT4d.

  • cT4b with extensive involvement of the skin.

  • cN0 with SLNB positive (pN+) that need to associate ALND:

  • cT3-T4b.

  • 2 lymph node macrometastasis if cTis, cT1 and cT2.

  • Patients who underwent mastectomy and it is not possible associate adjuvant radiotherapy.

  • cN1:

  • If primary surgery treatment.

  • After neoadjuvant systemic treatment, if there is not a clinical-radiological complete response and/or SLNB positive (ypN+).

  • cN2:

  • If primary surgery treatment.

  • After neoadjuvant systemic treatment, if luminal tumours or there is not a clinical-radiological complete response in triple negative or HER2 overexpressed tumours.

  • cN3.

Exclusion Criteria:
  • Patients with previous axillary surgery (except sentinel node biopsy)

  • Patients who did previous axillary radiotherapy treatment.

  • Patients who do not wish to participate in the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital de Bellvitge Hospitalet de Llobregat Barcelona Spain 08907

Sponsors and Collaborators

  • Hospital Universitari de Bellvitge

Investigators

  • Principal Investigator: Carlos Ortega ExpĆ³sito, MD, Bellvitge Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Amparo Garcia-Tejedor, Principal Investigator, Hospital Universitari de Bellvitge
ClinicalTrials.gov Identifier:
NCT05040685
Other Study ID Numbers:
  • PR139/21
First Posted:
Sep 10, 2021
Last Update Posted:
Aug 3, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Amparo Garcia-Tejedor, Principal Investigator, Hospital Universitari de Bellvitge

Study Results

No Results Posted as of Aug 3, 2022