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No Axillary sUrgical Treatment In Clinically Lymph Node Negative Patients After UltraSonography

No Axillary sUrgical Treatment In Clinically Lymph Node Negative Patients After UltraSonography[NAUTILUS]: A Prospective, Multicenter, Phase III Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04303715
Enrollment
1734
Registered
2020-03-11
Start date
2020-09-15
Completion date
2027-12-31
Last updated
2026-02-13

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

Conditions

Breast Cancer, Sentinel Lymph Node

Brief summary

NAUTILUS study is a prospective, multicenter, RCT. Clinically T1,T2, node negative BCS candidates with no evidence of metastases in AUS are 1:1 randomized into no SLNB group and SLNB group. NAUTILUS study aim to establish the minimally invasive treatment of breast cancer by reexamining the necessity of sentinel lymph node biopsy among patients with invasive breast cancer who have tumors under 5cm, are clinically node-negative, and are having breast conserving surgery performed.

Detailed description

\[Background\] Skipping ALND, the follow-up treatment in SN-positive patients, has non-inferior oncological outcomes compared to SLNB-only group, given that there is no severe SN metastases. Axillary ultrasound can effectively exclude high nodal burden, showing 95% NPV in a systematic review. SLNB has morbidity including lymphedema, limited range of motion, pain, and other post-surgical complications, eventually leading to reduced quality of life. Considering improvement of imaging modalities and adjuvant care, survival outcome of SLNB must be re-evaluated. Especially research reflective of the regional specificities of Korea and Asia-Pacific is needed. \[Study design\] Prospective, Multicenter, RCT. \[Statistical considerations\] According to Z0011 trial, 5yr DFS in eligible patients is expected to be 86%, which is between previous data of 88.6% in cT1,2 and SN-negative patients4, and 83.9% in cT1,2 and 1-2 SN-positive patients. Non-inferiority margin is set at 5%. With 5% significance level and 80% power, 780 patients are needed in each group. Assuming a 10% drop out rate, 1734 patients need to be recruited. \[Screening and Randomization\] Participants undergo screening tests that assess eligibility according to inclusion/exclusion criteria. In order to identify axillary lymph node metastases, axillary ultrasound is first performed by radiologists. Patients showing normal features are enrolled, while for conditionally normal patients, with only 1 suspicion of low nodal burden, axillary lymph node biopsy should be performed. Suspicious patients are excluded under following conditions: patients with 1 or more suspicion of high nodal burden, 2 or more suspicion of low nodal burden, or T2 invasive lobular carcinoma patients with 1 or more low nodal burden. The severity of nodal burden is defined through the criteria. Patients who underwent radiological axillary staging are randomly assigned (1:1) to the study arm and the control arm before surgical care. Stratification is done based on trial centers and tumor sizes. \[Post-surgical care\] All patients are planned to receive ipsilateral whole breast radiation. Patients randomized to non-SLNB arm are recommended to follow high tangential radiotherapy protocol, in which upper margin of radiation field includes axillary level I and II or lies within 2CM from humeral head. Additional treatment may be performed if deemed necessary by the researcher \[Objectives\] 1. Primary objective \- 5yr Disease Free Survival 2. Secondary objectives * 5yr Overall Survival * 5yr Distant Metastasis Free Survival * Axillary recurrence rate * Patient reported AE * QoL

Interventions

PROCEDURENo SLNB

BCS only. Ommission of SLNB by axilla ultrasonography among selective breast cancer patients

PROCEDURESLNB

BCS with SLNB(+/-ALND)

Sponsors

Seoul National University Hospital
Lead SponsorOTHER
National Evidence-Based Healthcare Collaborating Agency
CollaboratorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Women ≥ 19 years * Invasive unilateral breast carcinoma with histological confirmation * History of invasive breast cancer * Histologically or radiologically no suspicion of distant metastases * Performance status corresponding to ECOG grade 0-2 * Tumor size clinically and radiologically ≤ 5cm, independent of hormone receptor and HER2 status * Clinically and sonographically negative axillary lymph nodes before biopsy; core needle biopsy or fine needle aspiration of suspicious lymph node required * BCS candidate with postoperative whole-breast irradiation and adequate systemic therapy * No psychological and geographical restriction in follow-up * Written informed consent

Exclusion criteria

* History of any cancer in the previous 5 years * Bilateral breast cancer * Invasive breast cancer treated with neoadjuvant therapy * Tumor size clinically and radiologically \> 5cm * Mastectomy candidate * Pregnancy and breastfeeding * Male breast cancer * Unable to understand and fill out questionnaires

Design outcomes

Primary

MeasureTime frameDescription
Disease Free Survival (DFS)5 yearsEvaluate 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
Patient reported Adverse Events (AEs)1 yearEvaluate Patient reported Adverse Events
QoL1 yearEvaluate Quality of Life of patient by EORTC QLQ-C30 questionnaire

Countries

South Korea

Contacts

PRINCIPAL_INVESTIGATORWonshik Han

Seoul National University Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026