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NCT Number: NCT05314114

Selective Omission of Axillary Surgery in Triple-negative and HER2-positive Breast Cancer After NACT

Neoadjuvant chemotherapy (NACT) is standard treatment for many triple-negative (TNBC) and HER2-positive breast cancer. Study showed about half of the biopsy-proven axillary disease will be eradicated by NACT and converted to ypN0 indicating the efficacy of systemic treatment in local disease control.

According to current guidelines, all initial cN0 patients will undergo sentinel lymph node biopsy (SLNB) after NACT and further axillary dissection (ALND) if tumor residual is discovered after SLNB. Data suggest patients who underwent SLNB have a significantly higher rate of disability in the early post-operative period compared to patients who did not and the avoidance of SLNB might translate into a considerable reduction of physical and emotional distress. Recent studies revealed the association between breast pCR and ypN0 status after NACT. Initially cN0 TNBC and HER2-positive breast cancer patients who achieve pCR in breast after NACT have a very low risk of positive lymph node residual and are very unlikely to benefit from further axillary surgery including SLNB.

The investigators designed a clinical trial to test the hypothesis that selective omission of axillary surgery in distinct responders after NACT will not deteriorate survival. In the planned trial, axillary surgery will be completely eliminated for initially cN0 TNBC and HER2-positive breast cancer patients who achieve pCR in breast after NACT determined by lumpectomy.

The trial is designed as a prospective, single-center, single-arm study with a limited number of patients (N=136). Patients will be recruited in China over a period of 36 months. Our results, together with other ongoing studies in other parts of the world with a similar design, might give practice-changing results and spare the time and the costs of a randomized comparison.

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Key information

Age range

18 year–70 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Peking University Cancer Hospital

Beijing, Beijing Municipality, 100142, China

Location status: Recruiting

Location contact

TAO OUYANG, M.D

CONTACT

[email protected]

0086-10-88196696

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Written informed consent
  • Core biopsy confirmed unicentric primary invasive triple-negative or HER2-positive breast cancer. Multifocal or multicentric tumors allowed only if breast-conserving surgery is deemed feasible.
  • At least 18 years of age
  • Initial tumor stage cT1c-T3N0M0 prior to NACT. cN0 stage established by clinical examination and ultrasonography
  • In cases with suspicious lymph node, a negative core biopsy or fine needle aspiration (FNA) biopsy of the sonographically suspected lymph node is required
  • Standard NACT with evident radiologic response
  • Planned breast-conserving surgery with postoperative external whole-breast irradiation

Exclusion criteria

  • History of previous malignancy
  • Histologically proven N1 patients, patients with distant metastasis (M1)
  • Pregnant or lactating patients
  • Inflammatory breast cancer
  • Radiologically non-responsive after NACT
  • Mastectomy planned after NACT
  • planned intraoperative radiotherapy (e.g. Intrabeam) or postoperative partial breast irradiation (e.g. multicatheter technique) alone; both procedures are allowed as boost techniques
  • Written informed consent not obtained

Treatment and study plan

No axillary surgery

Procedure

No axillary surgery

Primary outcomes

  1. ipsilateral axillary recurrence-free survival

    Time frame: 5-year

    time between randomization and confirmed ipsilateral axillary recurrence

Secondary outcomes

  1. locoregional lymph node recurrence-free survival

    Time frame: 5-year

    time between randomization and confirmed locoregional lymph node recurrence

  2. distant metastasis-free survival

    Time frame: 5-year

    time between randomization and confirmed distant metastasis

Sponsors and collaborators

Lead sponsor

Peking University

Other

Registry information

Official study title

Selective Omission of Axillary Surgery in Distinct Responders With Triple-negative and HER2-positive Breast Cancer After NACT

Important dates

Study start
2020
Primary completion
2023
Study completion
2028
First posted
Apr 6, 2022
Registry last updated
Apr 18, 2022

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.

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