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Sentinel lymph node surgery with contrast enhanced ultrasonography and blue dye methods after neoadjuvant chemotherapy in patients with node-positive breast cancer

Sentinel lymph node surgery with contrast enhanced ultrasonography and blue dye methods after neoadjuvant chemotherapy in patients with node-positive breast cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063788
Enrollment
Unknown
Registered
2022-09-16
Start date
2022-09-16
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

breast cancer

Interventions

Group 1 :Sentinel lymph node surgery with contrast enhanced ultrasonography and blue dye methods

Sponsors

Sichuan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Women aged 18-70 years; 2. According to the 7th edition of the American Joint Committee on Cancer (AJCC) staging system, primary invasive breast cancer with clinical stage of at least T0-4, N1-2, M0 before initial treatment; 3. ECOG score is 0 or 1; 4. Have completed or plan to receive neoadjuvant chemotherapy (the regimen is at the discretion of the patients medical team, and have received at least 6 cycles of neoadjuvant therapy containing anthracyclines and/or taxanes, and patients with HER-2 positive breast cancer should receive a full course of anti-HER-2 therapy); 5. Axillary lymph node biopsy before chemotherapy confirmed positive lymph nodes; 6. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Breast cancer or inflammatory breast cancer during pregnancy; 2. History of previous axillary surgery (including patients with previous history of sentinel lymph node surgery or lymph node biopsy to pathologically confirm the status of the axillary); 3. According to the 7th edition of the American Joint Committee on Cancer (AJCC) staging system, patients with clinical stage of M1 or cN3 before initial treatment.

Design outcomes

Primary

MeasureTime frame
The false negative rate (FNR) for SLN surgery;

Countries

China

Contacts

Public ContactExian Mou

Sichuan Cancer Hospital

785203071@qq.com+86 18583671536

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026