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No Axillary Surgical Treatment in Clinically Lymph Node Negative Patients on Ultrasonography After Neoadjuvant Chemotherapy

No Axillary Surgical Treatment in Clinically Lymph Node Negative Patients on Ultrasonography After Neoadjuvant Chemotherapy: A Prospective, Phase III Clinical Trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06704945
Acronym
Neo-NAUTILUS
Enrollment
464
Registered
2024-11-26
Start date
2025-06-04
Completion date
2034-12-31
Last updated
2026-01-28

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

Conditions

Breast Cancer, Neoadjuvant Therapy, Sentinel Lymph Node Biopsy

Keywords

Omission of axillary surgery after neoadjuvant chemotherapy, Breast cancer, Neoadjuvant chemotherapy, De-escalation, Omission of surgery

Brief summary

NEO-NAUTILUS is a prospective, multicenter, randomized phase III clinical trial to evaluate whether omitting axillary lymph node surgery (ALND or SLNB) in clinically lymph node-negative breast cancer patients after neoadjuvant chemotherapy is non-inferior to performing SLNB in terms of 5-year disease-free survival.

Detailed description

Background: * No prospective studies have proven that axillary lymph node surgery improves survival in breast cancer patients. * The ACOSOG Z0011 trial showed that additional axillary dissection did not improve recurrence or survival, even with a 23.7% incidence of non-sentinel node metastases. * NSABP B-32 established the oncologic safety of SLNB, significantly reducing complications like lymphedema compared to axillary dissection. However, SLNB still carries risks of lymphedema, sensory changes, seromas, and infections. * The trend has now shifted toward identifying candidates for omitting axillary surgery to minimize unnecessary complications. * The SOUND trial demonstrated non-inferiority of omitting SLNB in early-stage breast cancer patients with negative axillary ultrasound. Five-year distant metastasis-free survival was comparable between SLNB and no-SLNB groups (97.7% vs. 98.0%). * Improved ultrasound accuracy (e.g., FNR: 13.7% in SOUND; 11.3% in NAUTILUS) and the therapeutic contribution of whole-breast radiation likely support these findings. * Patients with a complete pathological response (pCR) in the breast post-NAC rarely have residual lymph node metastases, reducing the need for axillary surgery. * Single-arm studies (e.g., EUBREAST-01, ASICS, ASLAN) have explored omitting axillary surgery in patients with confirmed breast pCR. However, these studies face limitations due to small sample sizes, single-arm design, and the necessity of axillary surgery if pCR is not achieved. * To address these limitations, the NEO-NAUTILUS trial proposes the first randomized trial to compare disease-free survival and local recurrence rates between patients who omit SLNB (experimental group) and those who undergo SLNB (control group) after NAC, focusing on patients deemed axillary node-negative by ultrasound.

Interventions

BCS only. Ommission of axillary surgery. No axillary surgery after neoadjuvant chemotherapy.

BCS with SLNB(+/-ALND)

Sponsors

Seoul National University Hospital
Lead SponsorOTHER
Asan Medical Center
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Women aged ≥19 years. * Histologically confirmed invasive breast carcinoma treated with neoadjuvant chemotherapy. * Clinical staging prior to NAC: cT1-3, cN0, M0 (AJCC 8th Edition). * If pre-NAC staging is cT1-3, cN1, M0, must meet the following criteria: 1. HER2-positive or triple-negative breast cancer (TNBC). 2. At least 30% reduction in tumor size on MRI after NAC (comparing pre- and post-NAC MRI). * Negative axillary lymph node status on ultrasound after NAC. * Planned for breast-conserving surgery with completed neoadjuvant chemotherapy (at least half the planned regimen must be completed). * ECOG performance status of 0-2. * Signed written informed consent before enrollment.

Exclusion criteria

* History of any cancer within the past 5 years. * Bilateral breast cancer. * Patients requiring mastectomy. * Tumor size \>5 cm after NAC. * Male breast cancer. * Pregnant or breastfeeding women. * Inability to understand and complete questionnaires.

Design outcomes

Primary

MeasureTime frameDescription
Invasive Disease Free Survival (iDFS)5 yearsEvaluate invasive disease free survivals

Secondary

MeasureTime frameDescription
Overall Survival (OS)5 yearsEvaluate overall survival
Distant Metastasis Free Survival (DMFS)5 yearsEvaluate distant metastasis free survival
Axillary recurrence rate5 yearsEvaluate ipsilateral axillary recurrence rate
Locoregional Recurrence Rate (LRR)5 yearsEvaluate locoregional recurrence rate
QoL1 yearEvaluate Quality of Life of patient by EORTC QLQ-C30 questionnaire

Countries

South Korea

Contacts

CONTACTWonshik Han, MD, PhD.
hanw@snu.ac.kr82-2-3461-6060

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026