Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06518135

Axillary Sentinel Lymph Node Biopsy After Neoadjuvant Chemotherapy in Patients With Initial cN1 Breast Cancer

SLNB has been recommended by domestic and foreign guidelines for patients with initial cN1 and NAC descending to ycN0. However, the best technical path is still not very clear at present, and the long-term tumor safety data is still insufficient. Therefore, it is necessary to further explore the optimal technical pathway and long-term tumor safety for SLNB in patients with initial cN1 and NAC downgrading to ycN0 in the real world.This study will evaluate the optimized technical pathway and long-term tumor safety of SLNB in patients with initial cN1 and NAC downgrading to ycN0 in real-world studies.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Henan cacer hospital

Henan, 450008, China

Location status: Recruiting

Location contact

Liu Zhen

CONTACT

13838308034

About this study

SLNB has been recommended by domestic and foreign guidelines for patients with initial cN1 and NAC descending to ycN0. However, the best technical path is still not very clear at present, and the long-term tumor safety data is still insufficient. Therefore, it is necessary to further explore the optimal technical pathway and long-term tumor safety for SLNB in patients with initial cN1 and NAC downgrading to ycN0 in the real world.This study will evaluate the optimized technical pathway and long-term tumor safety of SLNB in patients with initial cN1 and NAC downgrading to ycN0 in real-world studies. The main endpoint of the study was axillary recurrence free survival. The secondary study endpoints were regional lymph node recurrence free survival, disease-free survival, overall survival, incidence of postoperative upper limb lymphedema, and patient quality of life.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients With ECOG Score 0-1 Points
  • Patients With Breast Cancer Stage cT1-3N1M0 (According to AJCC Version 7) Pathological Diagnosis of Ipsilateral Axillary Lymph Node Metastasis in Patients With Invasive Breast Cancer
  • Patients With Abnormal Axillary Lymph Nodes ≤ 3 Detected by Imaging Examination
  • Patients With Effective Neoadjuvant Therapy (CR+PR)
  • Patients With Clinical Axillary Negative ycN0 After Neoadjuvant Therapy
  • Patients Without Prior History of Ipsilateral Axillary Surgery and Radiation Therapy
  • Patients Without Previous History of Ipsilateral Breast Cancer (Including Carcinoma in Situ)
  • Patients Without Obvious Contraindications for Surgery or Radiation Therapy
  • No Other History of Malignant Tumors Within 5 Years From Enrollment in the Study
  • Patients Who Participate in Other Clinical Trials at the Same Time and Are Judged by the Researchers Not to Affect the Study Protocol Can be Enrolled Normally
  • The patient voluntarily joined this study and signed an informed consent form.

Exclusion criteria

  • Stage IV (metastatic) breast cancer;
  • Simultaneous double breast cancer;
  • Baseline cT4;
  • Baseline cN2-3
  • gestation
  • There are contraindications for SLNB;
  • Suffering from serious comorbidities or other comorbidities that may interfere with the planned treatment, or any other circumstances in which the researcher deems the patient unsuitable to participate in this study

Treatment and study plan

SLNB group

Other

After the completion of neoadjuvant therapy, axillary SLNB should be performed first before breast surgery; If the frozen pathology SLNs are negative, ALND will no longer be performed; If frozen pathological SLNs are positive, ALND should be performed directly; If frozen pathology is false negative.

Other names: experimental group

Primary outcomes

  1. Axillary recurrence-free survival

    Time frame: 5th year after surgery

    The time from surgery to axillary recurrence or last follow-up

Secondary outcomes

  1. regional lymph node recurrence-free survival

    Time frame: 5th year after surgery

    The time from surgery to the occurrence of regional lymph node recurrence, metastasis, or last follow-up

  2. Disease-free survival

    Time frame: 5th year after surgery

    The time from surgery to the occurrence of recurrence, metastasis, or last follow-up

  3. Overall survival

    Time frame: 5th year after surgery

    The time from surgery to patient death or last follow-up

  4. The incidence of postoperative upper limb lymphedema

    Time frame: 5th year after surgery

    By using the circumference method, the styloid process of the ulna is taken as the starting point, with an interval of 10cm and measured up to 40cm. The circumference is measured, and the volume of the affected limb is ≥ 10% or>200ml.

  5. EORTC-QLQ-C30 V3 rating

    Time frame: 5th year after surgery

    The EORTC-QLQ-C30 V3 is the core scale of the quality of life measurement system developed by the European Organization for Research and Treatment of Cancer (EORTC) for cancer patients.

    The scale consists of 30 items, including 5 functional scales (physical function, role function, cognitive function, emotional function, social function), 3 symptom scales (fatigue, pain, malignant vomiting), 6 individual measurement items (swallowing difficulties, loss of appetite, sleep disorders, constipation, diarrhea, economic difficulties), and 1 patient self-assessment item (overall health status).

    The original scores for each item need to be converted into standardized scores ranging from 0 to 100 using a linear formula. The higher the score for each functional dimension, the better the functional status; The higher the score of the symptom scale and individual items, the more obvious the symptoms and the poorer the quality of life.

Study contacts

Contact information is provided by the study sponsor or research team.

Minhao Lv

CONTACT

0371-65587406

Zhenzhen Liu

CONTACT

[email protected]

0371-65587005

Sponsors and collaborators

Lead sponsor

Henan Cancer Hospital

Other Gov

Registry information

Official study title

Axillary Sentinel Lymph Node Biopsy After Neoadjuvant Chemotherapy in Patients With Initial cN1 Breast Cancer: a Prospective, Multicenter, Single Arm, Real World Study

Important dates

Study start
2024
Primary completion
2028
Study completion
2028
First posted
Jul 24, 2024
Registry last updated
Dec 17, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.