MUTAS: MUltimodal Targeted Axillary Surgery

Sponsor
Parc de Salut Mar (Other)
Overall Status
Recruiting
CT.gov ID
NCT04039893
Collaborator
GEICAM (Other)
160
1
1
36.8
4.4

Study Details

Study Description

Brief Summary

The present trial will prospectively evaluate the accuracy of both a systematic predefined axillary ultrasound imaging together with tumor load quantification of suspicious and sentinel axillary lymph nodes to predict overall tumor load in the axilla.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Systematic axillary ultrasound imaging
  • Diagnostic Test: Sentinel node
  • Procedure: Excision of suspicious lymph nodes
  • Procedure: Two steps axillary node clearance
N/A

Detailed Description

Axillary node clearance (ANC) is a controversial intervention in the surgical treatment of breast cancer. Different studies have shown that in some patients with infiltrated axillary lymph nodes but low tumor burden, ANC can be safely omitted. However, indications for ANC persist in nowadays for patients with positive axillary lymph nodes and upfront surgery and patients with positive lymph nodes after neoadjuvant treatment. The present prospective study will evaluate the ability to establish an axillary tumor load with two steps. The first step will be a preoperative predefined systematic axillary ultrasound imaging workflow. The second step will be the tumor load evaluation of suspicious and sentinel axillary lymph nodes. We will also evaluate which patients have infiltrated nodes only beneath the second intercostobrachial nerve. The trial intends to identify patients for who a complete axillary node clearance could be spared.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
160 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Prospective Trial to Evaluate MUltimodal Targeted Axillary Surgery (MUTAS) Approaches in Breast Cancer Patients With Positive Lymph Nodes.
Actual Study Start Date :
Oct 23, 2019
Anticipated Primary Completion Date :
Mar 15, 2022
Anticipated Study Completion Date :
Nov 15, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: Node-positive breast cancer patients

All patients with positive lymph nodes for who an axillary node clearance is proposed as part of the surgical treatment

Diagnostic Test: Systematic axillary ultrasound imaging
Before surgery, all patients will be explored with a pre-defined systematic and reproducible axillary ultrasound imaging workflow intending to establish the number of neoplastic lymph nodes.

Diagnostic Test: Sentinel node
Sentinel nodes will be identified with a radioisotope tracer and blue dye or fluorescein.

Procedure: Excision of suspicious lymph nodes
Nodes suspected to be infiltrated both by physical exploration and/or ultrasound will be excised and evaluated separately.

Procedure: Two steps axillary node clearance
Axillary node clearance will be performed in two steps comprising inferior and superior clearance. The second intercostobrachial nerve will be considered the limit defining the border between superior and inferior axilla.

Outcome Measures

Primary Outcome Measures

  1. Number of patients correctly identified as low axillary tumor load carriers by a pre-defined systematic axillary ultrasound imaging workflow [24 months]

    The accuracy (in terms of sensibility, specificity, positive predictive value and negative predictive value) of the pre-defined systematic ultrasound imaging workflow for identifying patients wih low axillary tumor load will be reported. Low axillary tumor load is defined as two or less infiltrated axillary lymph nodes.

  2. Number of patients correctly identified as low axillary tumor load carriers by the information on tumor load of suspicious and sentinel axillary lymph nodes. [24 months]

    The accuracy (in terms of sensibility, specificity, positive predictive value and negative predictive value) of different tumor load cut-off points of the suspicious and sentinel axillary lymph nodes for identifying patients with low axillary tumor load will be reported.Low axillary tumor load is defined as two or less infiltrated axillary lymph nodes.

  3. Number of patients correctly identified as low axillary tumor load carriers combining both the pre-defined axillary ultrasound imaging workflow with the information on tumor load of suspicious and sentinel axillary nodes [24 months]

    The accuracy (in terms of sensibility, specificity, positive predictive value and negative predictive value) of both the pre-defined systematic axillary ultrasound imaging workflow combined with tumor load information of suspicious and sentinel axillary lymph nodes for identifying patients with low axillary tumor load will be reported.Low axillary tumor load is defined as two or less infiltrated axillary lymph nodes.

Secondary Outcome Measures

  1. Number of infiltrated axillary lymph nodes detected by physical exploration [24 months]

    The difference between the number of positive lymph nodes identified in the final pathology exam and the nodes described as suspicious in physical exploration will be recorded to establish if physical exploration correctly estimates, underestimates or overestimates axillary tumour load.

  2. Number of infiltrated lymph nodes detected by computed tomography [24 months]

    The difference between the number of positive lymph nodes identified in the final pathology exam and the nodes described as suspicious in computed tomography will be recorded to establish if physical exploration correctly estimates, underestimates or overestimates axillary tumour load.

  3. Number of infiltrated lymph nodes detected by magnetic resonance [24 months]

    The difference between the number of positive lymph nodes identified in the final pathology exam and the nodes described as suspicious in magnetic resonance will be recorded to establish if magnetic resonance correctly estimates, underestimates or overestimates axillary tumour load.

  4. Number of patients with low axillary tumor load among menopause status categories [24 months]

    The number of patients with low axillary tumor load in each menopause category will be reported. Patients will be categorized according to their menopausal status (pre-menopause and menopause).

  5. Number of patients with low axillary tumor load among each breast cancer pathology subtype. [24 months]

    The number of patients with low axillary tumor load in each breast cancer pathology subtype (non-specified invasive carcinoma, lobular carcinoma and other carcinomas) will be reported

  6. Number of patients with low axillary tumor load among each breast cancer immunophenotype. [24 months]

    The number of patients with low axillary tumor load in each breast cancer immunophenotypes (luminal , Her2 positive and triple negative carcinomas) will be reported

  7. Number of patients with infiltrated nodes exclusively in the inferior axillary node clearance. [24 months]

    The number of patients with infiltrated nodes exclusively in the inferior axillary node clearance wil be reported. This information shall be obtained from the final pathology report.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Node-positive breast cancer patients confirmed by biopsy or cytology

  • Positivity confirmed before the surgical treatment

Exclusion Criteria:
  • Inability to confirm positive lymph nodes by biopsy or cytology

  • Inability to understand the protocol design

  • Poor understanding of the Spanish language

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital del Mar Barcelona Spain 08003

Sponsors and Collaborators

  • Parc de Salut Mar
  • GEICAM

Investigators

  • Principal Investigator: Maria Vernet-Tomas, MD, PhD, Parc de Salut Mar

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Parc de Salut Mar
ClinicalTrials.gov Identifier:
NCT04039893
Other Study ID Numbers:
  • 2018/8361/I
First Posted:
Jul 31, 2019
Last Update Posted:
Oct 15, 2021
Last Verified:
Oct 1, 2021
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
Keywords provided by Parc de Salut Mar
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 15, 2021