search
Back to results

De-escalating Axillary Surgery in Breast Cancer Patients in Nigeria

Primary Purpose

Breast Cancer, Axilla; Breast

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Sentinel lymph Node Biopsy
Sponsored by
Nova Scotia Health Authority
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring neoadjuvant, de-escalation, breast cancer, axillary lymph node staging

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Eligible to receive systemic chemotherapy Must include all the following: Tany, cN1 at presentation Biopsy proven pN1 disease after axillary US cN0 after neoadjuvant chemotherapy Exclusion Criteria: Previous / recurrent breast cancer Previous axillary and/or breast surgery Inflammatory breast cancer N2 disease or Stage IV disease

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Other

    Arm Label

    Sentinel Lymph Node Biopsy Arm

    Arm Description

    Patients with non-metastatic, biopsy and clipped locally advanced breast cancer will start systemic chemotherapy as per institutional best practices. Patients with a clinical complete response will be consented for SLNB followed by immediate ALND. Patients with persistent suspicious clinical adenopathy will be consented for ALND alone. All patients regardless of response to NAC will undergo ALND as per current institutional practices. Patients undergoing SLNB followed by ALND will have the procedure performed by study the co-PI at OAUTH who is trained in the performance of SLNB. Histopathologic assessment of the breast and axillary contents will follow a standardized reporting procedure, including the assessment of residual cancer burden in both the breast and the axilla. Presence or absence of residual disease will be reported separately for the SLNB specimens, clipped node and remaining axillary contents.

    Outcomes

    Primary Outcome Measures

    False-negative rate
    • False negative rate (FNR) of pre-op axillary US and single agent SLNB post-NAC for axillary staging

    Secondary Outcome Measures

    pathologic complete response rate
    • Incidence of axillary lymph node clinical and pathologic complete response in patient receiving NAC in Nigeria
    radiographic and clinical concordance
    • Concordance of pre-operative clinical, radiographic and pathologic lymph node status after NAC
    Sensitivity of pre-operative axillary US
    • Performance of pre-operative axillary US to stage the axilla in node positive patients who are cN0 disease after NAC
    Specificity of pre-operative axillary US
    • Performance of pre-operative axillary US to stage the axilla in node positive patients who are cN0 disease after NAC
    False negative rate of pre-operative axillary US
    • Performance of pre-operative axillary US to stage the axilla in node positive patients who are cN0 disease after NAC
    Sensitivity of single-agent sentinel lymph node biopsy
    • Performance of single agent SLNB using methylene blue to stage the axilla in node positive patients who are cN0 disease after NAC
    Specificity of single-agent sentinel lymph node biopsy
    • Performance of single agent SLNB using methylene blue to stage the axilla in node positive patients who are cN0 disease after NAC
    False negative rate of single-agent sentinel lymph node biopsy
    • Performance of single agent SLNB using methylene blue to stage the axilla in node positive patients who are cN0 disease after NAC

    Full Information

    First Posted
    April 11, 2023
    Last Updated
    September 13, 2023
    Sponsor
    Nova Scotia Health Authority
    Collaborators
    Obafemi Awolowo University
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT06039956
    Brief Title
    De-escalating Axillary Surgery in Breast Cancer Patients in Nigeria
    Official Title
    De-escalating Axillary Surgery After Neoadjuvant Chemotherapy in Node Positive Breast Cancer Patients in Nigeria
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    November 1, 2023 (Anticipated)
    Primary Completion Date
    May 31, 2025 (Anticipated)
    Study Completion Date
    May 31, 2028 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Nova Scotia Health Authority
    Collaborators
    Obafemi Awolowo University

    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
    In sub-Saharan Africa, breast cancer patients often present with advanced disease. In my previous research which evaluated over 600 patients from a prospective institutional data base, about 64% of women with a new diagnosis of breast cancer presented with locally advanced disease, including clinically positive axillary adenopathy. Our data also suggests that similar to African American women, triple negative breast cancer (TNBC) is common in Nigeria (43.5%). The overall goal of the project is to evaluate the ability of existing technology in Nigeria to safely de-escalate axillary surgery in the management of locally advanced breast cancer patients. Currently, the standard-of-care for breast cancer patients with palpable axillary adenopathy (clinical N1 disease without evidence of distant metastases) at presentation in Nigeria is neoadjuvant systemic therapy followed by a modified radical mastectomy. This includes a complete axillary lymph node dissection (ALND). However, data from high-income countries however show that up to 85% of patients initially presenting with cN1 disease can be converted to cN0 (i.e. no palpable adenopathy) following NAC. These patients can thus safely undergo sentinel lymph node biopsy (SLNB) with up to 50% of these having pathologic complete response in the lymph nodes. In this patient population, both methylene blue and radio-isotope localization with Tc-99 sulphur colloid are required to ensure adequate performance of the SLNB to stage the axilla(i.e. false negative rate ≤10%). Although widely available in high-income countries, radio-isotope localization is not readily available in Nigeria. This project will explore an alternative to dual agent SLNB localization using readily available resources and multi-disciplinary collaboration in a lower-income environment. De-escalation of axillary surgery in high-income countries has significantly decreased operative morbidity and improved patient reported outcomes without compromising survival. However, context specific research and data from resource limited environments is needed to translate the benefit of de-escalation to sub-Saharan Africa.
    Detailed Description
    The overall goal of my research is to promote the delivery of guideline-concordant breast cancer care to Nigerian breast cancer patients in a pragmatic manner. This project is novel in that the investigators are challenging the existing paradigm of dual agent localization, which is appropriate for a high-income setting, but completely out of reach and thus inapplicable in Nigeria despite the obvious need. I will leverage the African Research Group for Oncology (ARGO) breast cancer data base at OAUTHC and other existing research infrastructure to pursue the following specific aims: Aim 1: Determine the false negative rate of of axillary Ultrasound + single agent sentinel Lymph node biopsy in staging the axilla in cN1 patients who become cN0. The investigators will consent patients with complete clinical complete response (clinical assessment and targeted US) following NAC, for SLNB followed by immediate ALND. Presence or absence of residual disease will be reported separately for the SLNB and the ALND specimens. Positive axillary disease will be defined in a binary manner as any invasive disease (including isolated tumor cells) or not. Using ALND reporting as the gold standard, the investigators hypothesize a FNR of less than 10% following SLNB. Aim 2: To determine the proportion of patients with complete axillary LN Clinical &Pathological cR post NAC. The proportion of patients who return negative for cancer cells following SLNB and or ALND will be determined based on the number of patients with preoperative node positive disease. Both overall pCR and subgroup analysis based on receptor status will be done. The investigators will also assess the concordance of pre-operative clinical and radiographic (i.e. targeted axillary US) assessment of lymph node status with and pathologic lymph node status after NAC. The investigators hypothesize a pCR rate of 50% following completion of NAC This study will build on the peer-reviewed analysis of our own prospective data demonstrating a high incidence of locally advanced disease and chemo-sensitive subtypes (i.e. TNBC), which suggest that a large proportion of our patients may be candidates for de-escalation. The impact of de-escalation would be profound. Preliminary research into lymphedema as a result of ALND in our patient population suggest an incidence of > 35%. The proposed study will provide a strong foundation for future studies evaluating the implementation of this strategy and other resource compatible interventions on breast cancer outcomes in Nigeria.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Breast Cancer, Axilla; Breast
    Keywords
    neoadjuvant, de-escalation, breast cancer, axillary lymph node staging

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    Sentinel Lymph Node Biopsy Arm
    Arm Type
    Other
    Arm Description
    Patients with non-metastatic, biopsy and clipped locally advanced breast cancer will start systemic chemotherapy as per institutional best practices. Patients with a clinical complete response will be consented for SLNB followed by immediate ALND. Patients with persistent suspicious clinical adenopathy will be consented for ALND alone. All patients regardless of response to NAC will undergo ALND as per current institutional practices. Patients undergoing SLNB followed by ALND will have the procedure performed by study the co-PI at OAUTH who is trained in the performance of SLNB. Histopathologic assessment of the breast and axillary contents will follow a standardized reporting procedure, including the assessment of residual cancer burden in both the breast and the axilla. Presence or absence of residual disease will be reported separately for the SLNB specimens, clipped node and remaining axillary contents.
    Intervention Type
    Procedure
    Intervention Name(s)
    Sentinel lymph Node Biopsy
    Intervention Description
    The SLNB will be performed with 5 ml of undiluted methylene blue injected in equal aliquots, peri-tumoral, followed by a 5-minute massage prior to skin incision. Sentinel nodes will be defined as those that have uptake / visible blue staining or suspicious palpable nodes at the discretion of the operating surgeon. Sentinel nodes will be placed in formalin and sent separately. This will be followed by an immediate completion ALND, which will be similarly placed in formalin and sent separately from the SLNB specimen. Specimen radiographs will be performed on all specimens to confirm location of clip within SLNB vs. ALND specimens.
    Primary Outcome Measure Information:
    Title
    False-negative rate
    Description
    • False negative rate (FNR) of pre-op axillary US and single agent SLNB post-NAC for axillary staging
    Time Frame
    immediately after surgery
    Secondary Outcome Measure Information:
    Title
    pathologic complete response rate
    Description
    • Incidence of axillary lymph node clinical and pathologic complete response in patient receiving NAC in Nigeria
    Time Frame
    immediately after surgery
    Title
    radiographic and clinical concordance
    Description
    • Concordance of pre-operative clinical, radiographic and pathologic lymph node status after NAC
    Time Frame
    immediately after surgery
    Title
    Sensitivity of pre-operative axillary US
    Description
    • Performance of pre-operative axillary US to stage the axilla in node positive patients who are cN0 disease after NAC
    Time Frame
    immediately after surgery
    Title
    Specificity of pre-operative axillary US
    Description
    • Performance of pre-operative axillary US to stage the axilla in node positive patients who are cN0 disease after NAC
    Time Frame
    immediately after surgery
    Title
    False negative rate of pre-operative axillary US
    Description
    • Performance of pre-operative axillary US to stage the axilla in node positive patients who are cN0 disease after NAC
    Time Frame
    immediately after surgery
    Title
    Sensitivity of single-agent sentinel lymph node biopsy
    Description
    • Performance of single agent SLNB using methylene blue to stage the axilla in node positive patients who are cN0 disease after NAC
    Time Frame
    immediately after surgery
    Title
    Specificity of single-agent sentinel lymph node biopsy
    Description
    • Performance of single agent SLNB using methylene blue to stage the axilla in node positive patients who are cN0 disease after NAC
    Time Frame
    immediately after surgery
    Title
    False negative rate of single-agent sentinel lymph node biopsy
    Description
    • Performance of single agent SLNB using methylene blue to stage the axilla in node positive patients who are cN0 disease after NAC
    Time Frame
    immediately after surgery

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    70 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Eligible to receive systemic chemotherapy Must include all the following: Tany, cN1 at presentation Biopsy proven pN1 disease after axillary US cN0 after neoadjuvant chemotherapy Exclusion Criteria: Previous / recurrent breast cancer Previous axillary and/or breast surgery Inflammatory breast cancer N2 disease or Stage IV disease
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Gregory Knapp, MD
    Phone
    902-472-1523
    Email
    gregory.knapp@nshealth.ca
    First Name & Middle Initial & Last Name or Official Title & Degree
    Olalekan Olasehinde, MD
    Email
    lekanolasehinde@yahoo.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Olalekan Olasenhinde, MD
    Organizational Affiliation
    Obafemi Awolowo University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    De-escalating Axillary Surgery in Breast Cancer Patients in Nigeria

    We'll reach out to this number within 24 hrs