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Oncologic Safety of Sentinel Lymph Node Biopsy in Clinically Palpable Axillary Lymph Node in Breast Cancer Patients

Oncologic Safety of Sentinel Node Biopsy in Clinically Palpable Axillary Lymph Node in Breast Cancer Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05703295
Enrollment
40
Registered
2023-01-30
Start date
2023-02-28
Completion date
2025-03-31
Last updated
2023-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sentinel Lymph Node Biopsy

Keywords

Breast cancer

Brief summary

Evaluation patients with palpable lymph node with breast cancer by sentinel lymph node biopsy and how to affect on the management of breast cancer.

Detailed description

Breast cancer is the most common type of cancer in females and the 3rd leading cause of cancer mortality. One of the important aspects of breast cancer management is axillary staging and the status of axillary lymph nodes is an important prognosticator that affects adjuvant treatment decisions in patients with early breast carcinoma. Sentinel lymph node biopsy (SLNB), is considered to be the standard of care for node negative breast cancer, as it can save patients from the complications of axillary lymph node dissection (ALND). These complications include lymphedema, arm stiffness, and neuralgia, all of which significantly affect the patient's quality of life and raise healthcare costs. It also allows accurate axillary staging with minimal morbidity. Oncologic outcomes in terms of disease-free survival, overall survival, and locoregional recurrence rate were similar in the SLNB alone versus the ALND group in patients with clinically node-negative axilla. In doing the SLNB, a combination of radioactive technetium-99m and blue bye technique is preferred to increase the SLN identification rate than using one technique in isolation. The rationale for performing upfront SLNB as routine for patients being treated for breast cancer should be challenged, for this our study aiming for evaluation of the role of sentinel lymph node biopsy in management of breast cancer.

Interventions

PROCEDUREBiopsy

Sentinel lymph node biopsy

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

1. age more than 18 years. 2. fit for surgery. 3. Patients with no previous breast surgery. .

Exclusion criteria

1. patients less than 18 years. 2. patients unfit for surgery . 3. patients with advanced breast cancer. 4. Patients with previous breast surgery.

Design outcomes

Primary

MeasureTime frameDescription
Oncologic safety of sentinel node biopsy in clinically palpable axillary lymph node in breast cancer patientsbaselineEvaluation patients with palpable lymph node with breast cancer by sentinel lymph node biopsy and how to affect on the management of breast cancer.

Contacts

Primary ContactMohamed Ibrahim Mohamed
mohammedibraheem22@yahoo.com01002844642
Backup ContactMostafa Thabet Ahmed, Professor
mostafaharera@yahoo.com01002798144

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026