← Back to Clinical Trials
Recruiting NCT04741737

NCT04741737 Repeat Sentinel Lymph Node Biopsy in Ipsilateral Breast Tumor Recurrence

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT04741737
Status Recruiting
Phase
Sponsor Gangnam Severance Hospital
Condition Mastectomy
Study Type INTERVENTIONAL
Enrollment 532 participants
Start Date 2020-03-01
Primary Completion 2024-01-31

Eligibility & Interventions

Sex Female only
Min Age 19 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
reSLNB arm

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 532 participants in total. It began in 2020-03-01 with a primary completion date of 2024-01-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

According to the standard treatment guidelines established until recently, in the case of ipsilateral breast tumor recurrence without systemic metastasis, salvage mastectomy or lumpectomy can be performed when either partial or whole breast radiation therapy is possible. On the other hand, there are currently no standard treatment guidelines for axillary treatment, and the evidence for this is limited. Axillary lymph node metastasis was reported to occur in about 26% of breast cancer patients who had negative sentinel lymph nodes from previous surgery for primary breast cancer and only local recurrence occurred. It is still important in the decision of treatment or adjuvant radiation therapy. However, it is known that most of the patients with ipsilateral breast recurrence do not have axillary lymph node metastasis. Therefore, performing axillary axillary surgery in all of these patients does not help the patient's survival in many cases, but rather can lead to complications such as lymphedema and seroma and postoperative wound infection. A question about the implementation of axillary lymph node resection has been raised and for this reason, it is necessary to study whether surveillance lymph node biopsy is still effective in patients with recurrence in the ipsilateral breast. Most of the studies on ipsilateral breast tumor recurrence without systemic metastasis reported to date are case reports or small retrospective studies. In addition, the combined meta-analysis also has limitations in that the study design is not uniform, and there are many cases in which primary breast cancer surgery performed total mastectomy or axillary lymph node dissection. This study is a multicenter prospective study designed to validate the clinical effectiveness of repeat-SLNB conducted in patients with ipsilateral breast tumor recurrence among patients who previously underwent breast conservation and sentinel lymph node biopsy for unilateral primary breast cancer.

Eligibility Criteria

Inclusion Criteria: 1. Age over 19 years old 2. Patients who are expected to undergo surgery under the diagnosis of ipsilateral breast tumor recurrence(histologically confirmed in situ disease or invasive disease) 3. Patients who had partial mastectomy and sentinel lymph node biopsy for prior operation for the initially diagnosed breast cancer 4. Patients considered to be axillary lymph node negative from clinical findings 5. Patients who understand and willingly participate in the study Exclusion Criteria: 1. Patients with recurrence in other regions. (e.g. ipsilateral axillary lymph node, supraclavicular lymph node, internal mammary lymph node, etc.) 2. Patients who are not eligible to perform SLNB 3. Patients who received mastectomy or axillary lymph node dissection for prior operation 4. Patients who experienced recurrence within a year from the primary operation 5. Patientes who are known to have axillary lymph node metastasis before the secondary operation, histologically confirmed from tissue biopsy or cytology 6. Patients with systemic recurrence 7. Patients with inflammatory breast cancer 5\) Pregnant and lactating patients

Contact & Investigator

Central Contact

Soong June Bae, M.D.

✉ mission815815@yuhs.ac

📞 82-2-2019-4401

Principal Investigator

Joon Jeong

PRINCIPAL INVESTIGATOR

Gangnam Severance Hospital, Yonsei University College of Medicine

Frequently Asked Questions

Who can join the NCT04741737 clinical trial?

This trial is open to female participants only, aged 19 Years or older, studying Mastectomy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04741737 currently recruiting?

Yes, NCT04741737 is actively recruiting participants. Contact the research team at mission815815@yuhs.ac for enrollment information.

Where is the NCT04741737 trial being conducted?

This trial is being conducted at Seoul, South Korea.

Who is sponsoring the NCT04741737 clinical trial?

NCT04741737 is sponsored by Gangnam Severance Hospital. The principal investigator is Joon Jeong at Gangnam Severance Hospital, Yonsei University College of Medicine. The trial plans to enroll 532 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology