Using photo-medicine to guide reoperation for lymph nodes in recurrent breast cancer
Official title: Photo-medicine-Guided Dual Approach for Reoperation of Sentinel Lymph Nodes in Locally Recurrent Breast Cancer Patients
Run by National Cancer Center, Korea · NCT06780748 · Data updated 2026-11-12
This study is testing a new method using light to help doctors find lymph nodes during surgery for women with recurrent breast cancer to see if it improves treatment planning.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 30 (estimated) |
| Sponsor | National Cancer Center, Korea Government |
| Locations | 1 site (Goyang-si) |
| Status | Recruiting |
| Started | August 13, 2023 |
| Main results expected | December 31, 2025 |
| Study ends | December 31, 2025 |
| Registry record updated | January 17, 2025 |
| Trial ID | NCT06780748 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are female patients aged 18 or older with ipsilateral locally recurrent breast cancer who have previously undergone axillary surgery.
✕Probably not a fit
Patients with distant metastases or those who have undergone ipsilateral mastectomy will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial investigates a dual approach using photo-medicine to guide the reoperation of sentinel lymph nodes in patients with locally recurrent breast cancer. The study aims to improve the identification rate of sentinel lymph nodes, which is crucial for effective staging and treatment planning. Participants will include female patients aged 18 and older who have previously undergone axillary surgery for breast cancer. The trial seeks to clarify the role of sentinel lymph node biopsy in the surgical management of recurrent cases, which remains uncertain according to current guidelines.
Why it matters
Potential benefit: If successful, this approach could enhance surgical outcomes and reduce complications for patients with recurrent breast cancer.
How similar studies have gone: Recent studies have shown promising outcomes for repeat sentinel lymph node biopsy, indicating potential success for this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with ipsilateral locally recurrent breast cancer who previously underwent ipsilateral axillary surgery. * Female patients aged 18 years or older. * Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. * Patients who voluntarily decide to participate in the study and provide written informed consent. Exclusion Criteria: * Patients with distant metastases. * Patients who previously underwent ipsilateral mastectomy. * Pregnant or breastfeeding women. * Patients with a general condition that impairs the ability to understand or provide informed consent.
Where it's running
-
National Cancer Center
Goyang-si, South Korea Recruiting
Study contacts
- Principal investigator: Seeyoun Lee — National Cancer Center, Korea
- Study coordinator: Seeyoun Lee
- Phone: +82-31-920-1736
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Using indocyanine green to find sentinel lymph nodes during mastectomy
This pilot will test whether injecting indocyanine green and using fluorescence during mastectomy can find sentinel lymph nodes in women with clinically node-negative invasive breast cancer.
-
Using indocyanine green to identify sentinel lymph nodes during breast cancer surgery
This project tests whether indocyanine green dye and a fluorescence camera can be used instead of the radioactive tracer to find sentinel lymph nodes in adults having breast cancer surgery who are clinically node-negative.
-
Targeted sentinel node biopsy for breast cancer patients with limited axillary nodal disease
This audit will test if removing the marked node along with the sentinel nodes can identify people with only 1–2 positive axillary nodes so some can avoid a full axillary dissection, for adults with cT1-2 breast cancer and biopsy-proven axillary metastases with no more than two abnormal nodes on imaging.
-
Gyrotonic exercise for elders with breast cancer and Behcet disease
We’re testing whether a gyrotonic exercise program helps older people who have both Behcet disease and breast cancer.
-
PECS II vs SPSIP nerve blocks for pain after mastectomy
This study tests whether two ultrasound-guided nerve blocks (PECS II and SPSIP) differ in how much opioid patients need after mastectomy.
-
CG-7321: a first-in-human test in advanced solid tumors
We’re testing CG-7321 alone and with fulvestrant to see if it’s safe and tolerable in adults with advanced solid tumors.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.